UNITED STATES SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-K

(Mark One)

[X]

☒        ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE

SECURITIES EXCHANGE ACT OF 1934

For the fiscal year ended December 31, 2014

2017

OR

[  ]TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

☐          TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from ______________ to _____________

Commission file number: 0-11635

000-11635

PHOTOMEDEX, INC.FC GLOBAL REALTY INCORPORATED

(Exact name of registrant as specified in its charter)

 
Nevada
59-2058100
(State or other jurisdiction
Other Jurisdiction
(I.R.S. Employer
of incorporation or organization)Organization)
59-2058100
(I.R.S.  Employer
Identification No.)

100 Lakeside Drive,40 Ramland Road South, Suite 100, Horsham, Pennsylvania 19044200 Orangeburg, NY 10962

(Address of principal executive offices, including zip code)

(215) 619-3600

(Issuer'sIssuer’s telephone number, including area code)

Securities registered under Section 12(b) of the Exchange Act:


 
Name of each exchange
Title of each class
Common Stock
 
Name of each exchange
on which registered
Nasdaq Global Select Market, TASE
 
Common StockNasdaq Capital Market, TASE

Securities registered under Section 12(g) of the Exchange Act:

None
(Title of Class)

Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act.

Yes []

Yes☐ No [X]


☒ 

Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Exchange Act.

Yes []

Yes☐ No [X]



☒ 

Indicate by check mark whether the registrant: (i) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (ii) has been subject to such filing requirements for the past 90 days.


Yes [X]   No [__]


Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein and will not be contained, to the best of registrant's knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K or any amendment to this Form 10-K.

Yes [X] No [__]

☐ 

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).


Yes [X] No [__]


☐ 

Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein and will not be contained, to the best of registrant’s knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K or any amendment to this Form 10-K.

Yes ☒  No ☐

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company, or emerging growth company. See the definitions of "large“large accelerated filer," "accelerated filer"” “accelerated filer,” “smaller reporting company,” and "smaller reporting company"“emerging growth company” in Rule 12b-2 of the Exchange Act.


Large Accelerated Filer ☐
Large accelerated filer [__]
Accelerated filer [X]
Filer ☐
Non-Accelerated Filer ☐   (Do not check if a smaller reporting company)
Non-accelerated filer [__]

Smaller reporting company [  ]

Emerging growth company ☐ 


If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐ 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act).


Yes [] No [X]


The number of shares outstanding of our common stock as☒ 

As of June 30, 2014, was 19,049,582 shares. The2017 (the last business day of the registrant’s most recently completed second fiscal quarter), the aggregate market value of the shares of the registrant’s common stock held by non-affiliates (11,790,039 shares), based on(based upon the closing marketsale price ($12.25)of such shares as reported on The Nasdaq Capital Market) was approximately $4.9 million. Shares of the registrant’s common stock asheld by each executive officer and director and by each person who owns 10% or more of June 30, 2014, was $144,427,978.


the outstanding common stock have been excluded from the calculation in that such persons may be deemed to be affiliates of the registrant. This determination of affiliate status is not necessarily a conclusive determination for other purposes. 

As of March 13, 2015,30, 2018, the number of shares outstanding of our common stock was 11,868,619. 

22,101,718DOCUMENTS INCORPORATED BY REFERENCE. The closing market price of our common stock as of March 13, 2015 was $1.70.

None. 






Table of Contents

Part I   
Page
Part I    



1
Item 1A. 3
Item 1A.Risk Factors 2518
Item 1B.  6329
Item 2.  6329
Item 3.  6430
Item 4  6631

 

 

 

 
Item 5.
 

66
Item 6. 
31
Item 6.Selected Financial Data 6832
Item 7.  6932
Item 7A.  8941
Item 8.  8941
Item 9.  8941
Item 9A.  9041
Item 9B.  9342

 

 

 

 
Item 10.
 

93
Item 11. 
42
Item 11.Executive Compensation 9949
Item 12.  10952
Item 13.  11154
Item 14.  11255

 

 

 

 
Item 15.
 


113
 
56
SignaturesItem 16. 119Form 10-K Summary60






i

CAUTIONARY

INTRODUCTORY NOTE REGARDING FORWARD-LOOKING STATEMENTS

Certain statements

Use of Terms

Except as otherwise indicated by the context and for the purposes of this report only, references in this Annual Report on Form 10-K,report to “we,” “our” and “our company” refer to FC Global Realty Incorporated (Formerly: PhotoMedex, Inc.), a Nevada corporation, and its consolidated subsidiaries.

Special Note Regarding Forward Looking Statements

This report and the other materials we have filed or this Report, are "forward-looking statements." Thesewill file with the U.S. Securities and Exchange Commission, or the SEC, contain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, or the Securities Act, and Section 21E of the Securities Exchange Act of 1934, as amended, or the Exchange Act. All statements, other than statements of historical fact, are statements that could be deemed forward-looking statements, including, but not limited to, statements regarding our business strategy, expectations and plans regarding our future operations and our future financial position. When used in this report or in the other materials we have filed or will file with the SEC, the words “believe,” “may,” “will,” “potentially,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “indicate,” “seek,” “project,” “plan,” “could,” “should” or “would” and similar expressions are intended to identify forward-looking statements. Among the factors that could cause or contribute to material differences between our actual results and those indicated from the forward-looking statements are risks and uncertainties inherent in our business, including, but not limited to:

our ability to successfully integrate the acquired real estate business;

our ability to retain key employees;

demand fluctuations in the real estate industry;

adverse changes in economic conditions in markets where our real estate investments may be made;

possible decreases in the market value of our future real estate investments;

our ability to obtain adequate financing to fund our future property acquisitions and project developments;

the possibility that we may not recover our advance costs in each real estate development project;

our reliance on subcontractors to construct each property, and on building supply companies to provide components for each property’s construction;

competition in the real estate industry;

the possibility that legal challenges or governmental regulations may delay the start or completion of construction on our projected real estate ventures, increase our expenses, or limit our construction activities;

the potential for increased costs or shortages of labor or components, or other circumstances beyond our control;

our ability to continue as a going-concern;

our ability to raise capital when needed;

economic, political or other developments in foreign countries in which we do business;

the international nature of our business; and

results of existing or future litigation.

Additional factors that could cause or contribute to such differences include, but are not limited to, statements about the plans, objectives, expectations and intentions of PhotoMedex, Inc., a Nevada corporation, (referred tothose discussed in this Report as "we," "us," "our", "registrant" or "the Company")report, and other statements contained in this Report that are not historical facts. Forward-looking statements in this Report or hereafter includedparticular, the risks discussed under Item 1A. “Risk Factors” and those discussed in other publicly available documents filedwe file with the Securities and Exchange Commission, or the Commission, reportsSEC. Except as required by law, we do not intend to our stockholders and other publicly available statements issued or released by us involve known and unknown risks, uncertainties and other factors which could cause our actual results, performance (financial or operating) or achievements to differ from the future results, performance (financial or operating) or achievements expressed or implied by such forward-looking statements. Such future results are based upon management's best estimates based upon current conditions and the most recent results of operations. When used in this Report, the words "will, " "expect," "anticipate," "intend," "plan," "believe," "seek," "estimate" and similar expressions are generally intended to identify forward-looking statements, becauseupdate these forward-looking statements involve risks and uncertainties. There are important factors that could causepublicly or to update the reasons actual results tocould differ materially from those expressed or implied byanticipated in these forward-looking statements, including our plans, objectives, expectations and intentions and other factors discussed under "Risk Factors." We undertake no obligation to update such forward-looking statements. These forward-looking statements include, but are not limited to, statements about:

forecasts of future business performance, consumer trends and macro-economic conditions;
descriptions of market and/or competitive conditions;
descriptions of plans or objectives of management for future operations, products or services;
our estimates regarding the sufficiency of our cash resources, expenses, capital requirements and needs for additional financing and our ability to obtain additional financing
our ability to protect our intellectual property and operate our business without infringing upon the intellectual property rights of others;
our ability to obtain and maintain regulatory approvals of our products;
anticipated results of existing or future litigation; and
descriptions or assumptions underlying or related to any of the above items.
even if new information becomes available in the future. In light of these risks, uncertainties and assumptions, risksthe forward-looking events and uncertainties, thecircumstances discussed in this report may not occur and actual results could differ materially and events discussedadversely from those anticipated or implied in the forward-looking statements contained in this Annual Report on Form 10-K might not occur. Investorsstatements. Accordingly, readers are cautioned not to place undue reliance on such forward-looking statements.

Stock Split

On September 7, 2016, we completed a 1-for-5 reverse stock split of our outstanding common stock. Accordingly, all share and per share information contained in this report has been restated to retroactively show the forward-looking statements,effect of that stock split. 

ii 

PART I

ITEM 1.BUSINESS.

Our Company

Our company, founded in 1980, is transitioning from its former business as a skin health company to a company focused on real estate development and asset management, concentrating primarily on investments in high quality income producing assets, hotel and resort developments, residential developments and other opportunistic commercial properties.

Until the recent sale of our consumer products division, we were a global skin health company providing integrated disease management and aesthetic solutions to dermatologists, professional aestheticians and consumers. Starting in 2014, we began to sell off certain business units and product lines and on January 23, 2017, we sold the last remaining major product line. Following this transaction, we had only minimal operations and assets remaining, of immaterial value to our company. We are in the process of liquidating the remaining legacy inventory and assets of this business line, after which speaktime we will no longer operate within the skin health business.

Following the Contribution Transaction described below, our focus is to build our company into a leading real estate, asset management and development company concentrating primarily on investments in high yield income producing assets and other opportunistic commercial properties via direct property ownership and asset management. Our objective is to generate long term net asset value growth while adhering to institutional best practices and a deep research process for all investments.

For income producing properties, we intend to acquire assets that provide recurring income with the potential for income growth over the long-term. We believe there can be an attractive risk/reward profile to such properties based on the location and the underlying creditworthiness of the tenants. We intend to use such income generation to fund additional acquisitions and development opportunities and general corporate purposes. In addition, we intend to invest in land assets that can be developed into income generating properties or properties for sale. We believe that our size and scale provide an opportunity to take advantage of smaller-tier assets that most traditional investors do not focus on due to size limitations, thus creating unique investment opportunities. In particular, we intend to target assets in secondary and tertiary markets that require minimal capital expenditures but generate initial unlevered cash flow yields that are higher than those in primary markets.

A second component of our investment strategy will revolve around sourcing asset management opportunities for which we would operate as an asset manager of real estate properties. We are not structured as a Real Estate Investment Trust “REIT”, thus we have the ability to retain earnings and to operate in real estate asset management, development and peripheral real estate activities, items that may be limited by REIT requirements. We will look to utilize our existing infrastructure to provide economies of scale to owners of real estate assets as we grow our portfolio over time.

Recent Developments

Contribution Transaction

On March 31, 2017, we entered into an Interest Contribution Agreement with First Capital Real Estate Operating Partnership, L.P., or the Contributor, First Capital Real Estate Trust Incorporated, or the Contributor Parent (the Contributor and the Contributor Parent are sometimes referred to in this report as the Contributor Parties), and FC Global Realty Operating Partnership, LLC, our wholly-owned subsidiary, or the Acquiror. The parties entered into amendments to the Interest Contribution Agreement on August 3, 2017, October 11, 2017 and December 22, 2017. Pursuant to the Interest Contribution Agreement, as amended (which we collectively refer to as the Contribution Agreement), the Contributor contributed certain real estate assets to the Acquiror. In exchange, the Contributor received shares of our common stock and newly designated Series A Convertible Preferred Stock as described below. We refer to this transaction as the Contribution Transaction.

On May 17, 2017 (referred to in this report as the Closing Date), the Contributor transferred $10 million of assets to the Acquiror, consisting of the following:

three vacant land sites intended for development as gas stations located in northern California,


a 75% interest in a limited liability company that owns a vacant land site intended for development as a gas station, located in northern California; and

a 100% interest in a limited liability company, which we refer to as the Avalon Interest, which owns a 17.9133% interest in a limited liability company called Avalon Jubilee LLC that owns property located in Los Lunas, New Mexico being developed as a single family residential development. As described below, the Contributor Parent agreed to transfer the Avalon Interest within 30 days following the Closing Date.

Pursuant to the terms and conditions of an Agreement to Waive Closing Deliverables, dated as of May 17, 2017, the Contributor agreed to deliver the Avalon Interest to the Acquiror, in up to two installments, on or before the thirtieth (30th) calendar day following the Closing Date. The transfer of both installments of the Avalon Interest was completed on June 26, 2017. Notwithstanding that the Contributor did not complete the transfer of the Avalon Interest to the Acquiror on the Closing Date, the parties agreed that the Acquiror would be entitled to all economic benefits of ownership of the Avalon Interest from and after the date of the Closing Date.

On January 12, 2018, we received a copy of a complaint, dated November 17, 2017, that was filed by Alpha Alpha, LLC in the Thirteenth Judicial District Court in the County of Valencia in the State of New Mexico against Avalon Jubilee, LLC, the holding company that owns the property in Los Lunas, New Mexico, HiTex, LLC, MCBB, LLC, Land Strategies, LLC, Ronald R. Cobb and John Does 1 – 5. The suit asks the court to, among other things, determine whether there have been unauthorized transfers of interest in Avalon Jubilee LLC; and declare who are the holders of interests in Avalon Jubilee LLC. Although the complaint does not name our company or any of its subsidiaries or specifically question our interest in Avalon Jubilee LLC, it raises questions about whether the transfers of interest leading to our acquisition of our interest in Avalon Jubilee LLC were properly made in accordance with the Avalon Jubilee operating agreement. We have begun an internal investigation into this matter and will disclose the results of that investigation once it has been completed. Although neither our company nor any of its subsidiaries is a party to litigation regarding this matter, we recognized an impairment expense of $862 thousand to account for our estimate of the impact that such litigation may have on the operations and fair value of the underlying asset.

The proposed gas station sites are located in Atwater and Merced, California and had an agreed upon value of $2.6 million. We intend to explore our options for the development of these properties. We may (i) lease a property to a developer who will handle all further development of the property, with our company receiving monthly lease payments from the developer; (ii) engage a contractor to develop a property to a certain level, then lease it to a developer which will handle the final development and leasing of the property, with our company receiving monthly payments from the developer; or (iii) engage a contractor to completely develop a property, then lease it directly to a tenant who will remit monthly lease payments back to us. The option or options selected for these properties will depend upon the types of tenants interested in operating gas stations and/or related ventures on those properties, as well as our capitalization and available financial resources. In these arrangements, the construction and/or management of the properties are or will be handled by third-party firms which specialize in such work. Therefore, we anticipate that we will not need to hire significant additional personnel to develop, maintain and manage these properties. As for funding for any costs associated with these properties’ development, although we cannot provide any assurance that we will be able to obtain funding, we will seek funding from one or more of the following potential sources funding from third-party investors, funding as a result of loans secured by the properties, or joint-funding arrangements with developers and/or managers of these properties.

The residential development in New Mexico consists of approximately 250, non-contiguous, single family residential lots and a 10,000 square foot club house. The agreed upon value of this property was approximately $7.4 million. This property already has a management and construction arrangement in place. We are the minority holder in that property, holding a 17.9% interest.

In exchange for these assets, we issued to the Contributor 879,234 shares of our common stock, which represented approximately 19.9% of our issued and outstanding common stock immediately prior to the Closing Date, at a per share value of $2.5183, or $2.2 million in the aggregate. We issued the remaining $7.8 million of the approximately $10 million consideration to the Contributor in the form of 123,668 shares of our newly designated non-voting Series A Convertible Preferred Stock. Each share of the Series A Convertible Preferred Stock is convertible into 25 shares of our common stock, subject to the satisfaction of certain conditions, including stockholder approval of such conversion.


The number of shares of common stock issued to the Contributor and to be issued upon conversion of the Series A Convertible Preferred Stock was determined by dividing the $10 million value of the assets by $2.5183, a specified price per share value which represents a 7.5% premium above the volume-weighted average price of all on-exchange transactions in our common stock executed on The Nasdaq Capital Market, during the forty-three (43) trading days prior to the trading day immediately prior to the public announcement of the transaction by our company and the Contributor Parent on March 31, 2017, as reported by Bloomberg L.P. We believe that the trading price of our common stock at the time of the Contribution Transaction represented the value of our prior medical device business and not our new real estate development business. The value of the contributed assets was arrived at by the mutual agreement of the parties after analyzing each of the assets in comparison to historical sales of similar land parcels. We also assumed the obligations of the Contributor and its affiliates under certain agreements covering the delivered assets, including an Operating Agreement of Central Valley Gas Station Development, LLC, a Delaware limited liability company, dated January 28, 2013, and all amendments thereto; the Operating Agreement of Avalon Jubilee, LLC, a New Mexico limited liability company, dated as of May 16, 2012, and all amendments thereto; a Development Services Agreement, dated September 15, 2015, by and between UR-FC Contributed Assets, LLC, a Delaware limited liability company, as owner, and Land Strategies, LLC, a Nevada limited liability company, as developer, with respect to real property owned by Avalon Jubilee, LLC; and a Construction Contract dated, November 19, 2014, between Central Valley Gas Stations Development, LLC, as owner, and First Capital Builders, LLC, as contractor, with respect to the project known commonly as Green Sands and Buhach Rd., Atwater, CA. The Acquiror expects to enter into amended operating agreements with respect to some or all of these entities. As of the filing of this report, the agreements have not been amended.

Additionally, we assumed those ancillary agreements, commitments and obligations with respect to the delivered assets specified in that certain Assignment and Assumption Agreement, dated as of May 17, 2017.

Under the Contribution Agreement, on the Closing Date our Board was required to consist of seven (7) persons of whom three (3) would be designated by our company, three (3) would be designated by the Contributor Parent, and one (1) nonaffiliated director would be selected by the other six (6) directors; provided, however, that at least four (4) of the members of the Board as so designated would be independent directors. In accordance with the foregoing, on the Closing Date, Lewis C. Pell, Dr. Yoav Ben-Dror and Stephen P. Connelly resigned from our Board, Dr. Dolev Rafaeli, Dennis M. McGrath and Michael R. Stewart were designated by our company, and Suneet Singal, Richard J. Leider and Dr. Bob Froehlich were designated by the Contributor Parent to serve as members of the Board. The seventh director, Darrel C. Menthe, was designated and appointed to the Board by the other directors. On March 4, 2018, Suneet Singal resigned from the Company’s Board of Directors and on the following day, March 5, 2018, Darrel Menthe also resigned from the Company’s Board of Directors. Their resignations were not in connection with any known disagreement with the Company on any matter. Under the provisions of the Stock Purchase Agreement dated December 22, 2017, as reported in the Company’s Current Report on Form 8-K, filed with the Securities and Exchange Commission on December 29, 2017, Opportunity Fund I-SS, LLC, or “Opportunity Fund” has notified the Company that it may exercise its right to appoint two replacement directors to the Company’s Board of Directors, but it has not yet done so. The two directorships resulting from such resignations currently remain vacant. See “Private Placement” below.

Additionally, the following officer changes became effective as of the Closing Date:

Dr. Dolev Rafaeli, Dennis McGrath, and Dr. Yoav Ben-Dror resigned from their positions as officers of our company and its subsidiaries and we acknowledged and agreed that such resignations constituted valid terminations of their respective employment agreements for “Good Reason” (as that term is defined in their respective employment agreements) and the Board consented to the waiver of the notice requirements and cure periods as described in their respective resignation letters and confirmed that each of Messrs. Rafaeli and McGrath are entitled to all of the compensation described in Section 7(c) of their respective employment agreements for the remainder of the term of such employment agreements;

Suneet Singal was appointed as Chief Executive Officer of our company and Stephen Johnson was appointed the Chief Financial Officer of our company (both of Messrs. Singal and Johnson have since resigned as officers of our company); and

Dr. Ben-Dror resigned as managing director of our foreign subsidiaries, including Radiancy (Israel) Limited and Photo Therapeutics Limited in the United Kingdom, and agreed to enter into a non-compete agreement with our company and support the transition of his respective Board duties in lieu of his agreement for lock-up of his shares, and he will be entitled to all his compensation through a term that matches the term of Messrs. Rafaeli and McGrath.

Closing of the Contribution Transaction was subject to customary closing conditions and certain other specific conditions, including the following: (i) the entry into a registration rights agreement requiring us to register for resale the shares being issued in connection with the Contribution Transaction; (ii) the entry into a lock up agreement that restricts the transfer of our shares that are held by certain of our affiliates and certain affiliates of the Contributor Parent; (iii) the restructuring of our Board as described above; (iv) the resignation of certain of our officers as described above; and (v) the entry into an employment agreement with Mr. Suneet Singal, who became our new Chief Executive Officer at the closing.

The Contribution Agreement contemplated that additional contributions would be made prior to December 31, 2017; however, the Contributor failed to satisfy the conditions precedent to those additional contributions before the December 31, 2017 deadline such that only the closing described above was completed.


We elected to early adopt ASU 2017-01,Business Combinations (Topic 805) Clarifying the Definition of a Business.Accordingly, the determination of whether the transaction represents a business combination was evaluated by applying ASU 2017-01 guidance. We have determined that the group of assets assumed do not include (and also, none of them on a stand-alone basis) include, an input and a substantive process that together significantly contribute to the ability to create output and thus it was determined that the contribution represents an acquisition of assets rather than a business combination. Accordingly, the total sum of the fair value of consideration given (i.e. the fair value of the equity interests issued) together with the transaction costs, was allocated to the individual assets acquired and liabilities assumed based on their relative fair values at the date of acquisition. Such allocation did not give rise to goodwill.

The terms of the Series A Convertible Preferred Stock are governed by a certificate of designation, or the Series A Certificate of Designation, filed by us with the Nevada Secretary of State on May 15, 2017. Pursuant to the Series A Certificate of Designation, we designated 3,000,000 shares of our preferred stock as Series A Convertible Preferred Stock. Following is a summary of the material terms of the Series A Convertible Preferred Stock:

Dividends. Except for stock dividends or distributions for which adjustments are made, holders of Series A Convertible Preferred Stock shall be entitled to receive dividends on shares of Series A Convertible Preferred Stock equal (on an as-if-converted-to-common-stock basis) to and in the same form as dividends actually paid on shares of the common stock when, as and if such dividends are paid on shares of the common stock. No other dividends shall be paid on shares of Series A Convertible Preferred Stock.

Liquidation. Upon any liquidation, dissolution or winding-up of our company, whether voluntary or involuntary, the holders of Series A Convertible Preferred Stock shall be entitled to receive out of the assets, whether capital or surplus, of our company the same amount that a holder of common stock would receive if the Series A Convertible Preferred Stock were fully converted (disregarding for such purposes any conversion limitations) to common stock immediately prior to such liquidation, which amount shall be paidpari passuwith all holders of common stock. We must mail written notice of any such liquidation to each holder not less than 45 days prior to the payment date stated therein.

Voting Rights. Except as otherwise provided in the Series A Certificate of Designation or as otherwise required by law, the Series A Convertible Preferred Stock shall have no voting rights. However, as long as any shares of Series A Convertible Preferred Stock are outstanding, we shall not, without the affirmative vote of the holders of a majority of the then outstanding shares of the Series A Convertible Preferred Stock, (a) alter or change adversely the powers, preferences or rights given to the Series A Convertible Preferred Stock or alter or amend the Series A Certificate of Designation, (b) amend our articles of incorporation or other charter documents in any manner that adversely affects any rights of the holders, (c) increase the number of authorized shares of Series A Convertible Preferred Stock, or (d) enter into any agreement with respect to any of the foregoing.

Conversion. Each share of Series A Convertible Preferred Stock shall be convertible, at any time and from time to time from at the option of the holder thereof, into that number of shares of common stock determined by dividing $62.9575 by the Conversion Price. The Conversion Price for the Series A Convertible Preferred Stock is equal to $2.5183, subject to adjustment as described in the Series A Certificate of Designation.

Payout Notes and Stock Grant Agreement

Under the Contribution Agreement, amounts due to Dr. Dolev Rafaeli and Dennis M. McGrath under their employment agreements, as well as amounts due to Dr. Yoav Ben-Dror for his services as a board member and officer of our foreign subsidiaries, were converted to convertible secured notes in the principal amounts of approximately $3.1 million, $0.98 million and $1.5 million, respectively, following approval from our stockholders on October 12, 2017 (which we refer to as the Payout Notes). The Payout Notes were due on October 12, 2018, carried a ten percent (10%) interest rate, payable monthly in arrears commencing on December 1, 2017, and were secured by a security interest in all of our assets pursuant to a security agreement that we entered into with the holders of the Payout Notes on October 12, 2017. The Payout Notes were convertible into shares of our common stock and we agreed to register the shares underlying the Payout Notes within thirty (30) days of issuance with best efforts to cause the registration statement covering such shares to become effective within one-hundred twenty (120) days of issuance. On November 14, 2017, we filed a registration statement on Form S-3 (which we refer to as the First Registration Statement) to register all shares that may be issued upon conversion of the Payout Notes, which was subsequently amended to include the Payout Shares issued under the Stock Grant Agreement described below.


On December 22, 2017, we entered into a stock grant agreement, or the Stock Grant Agreement, with Dr. Dolev Rafaeli, Dennis M. McGrath and Dr. Yoav Ben-Dror (collectively referred to herein as the Note Holders) to (i) cause the early conversion of the Payout Notes into an aggregate of 5,628,291 shares of our common stock (which we refer to as the Payout Shares), (ii) effectuate the release of all security interests associated with the Payout Notes, (iii) provide for the issuance of an aggregate of 1,857,336 additional shares of common stock to the Note Holders as consideration for the various agreements of the Note Holders contained in the Stock Grant Agreement (which we refer to as the Additional Shares), (iv) provide for certain cash payments to the Note Holders in amounts equal to the interest payments that would have been made to the Note Holders absent the conversion of the Payout Notes, (v) obtain the agreement of the Note Holders to provide certain support services to our company, and (vi) obtain the conditional resignation of certain of the Note Holders from our Board of Directors. Accordingly, the Payout Notes were paid in full.

Pursuant to the Stock Grant Agreement, we agreed to make twelve (12) monthly payments on the first of each month commencing on January 1, 2018 in the amounts of approximately $21, $7, and $10 thousand, respectively, to Messrs. Rafaeli, McGrath, and Ben-Dror, respectively (which we refer to as the Cash Payments). The Cash Payments are consideration for certain consulting services to be provided by the Note Holders specified in the Stock Grant Agreement.

As promptly as possible following entry into the Stock Grant Agreement, we are required to file a proxy statement and hold a special meeting of our stockholders to authorize and approve the issuance of the Additional Shares. We are required to issue the Additional Shares promptly, but in any event within ten (10) days after we obtain stockholder approval of such issuance. As of the date of this Annual Reportreport, we have not yet filed such proxy statement.

In furtherance of obtaining such stockholder approval, on December 22, 2017, the Contributor, the Note Holders and certain other significant stockholders of our company, including OFI (as defined under “Private Placement” below), entered into a shareholder voting support and confidentiality agreement, or the Note Holder Voting Agreement, pursuant to which such stockholders agreed to vote their shares in favor of the transactions contemplated by the Stock Grant Agreement, including the issuance to the Note Holders or their designees of common stock equal to 20% or more of the common stock or 20% or more of the voting power outstanding before the issuance (which we refer to as the Note Holder 20% Proposal), and also agreed to certain transfer restrictions on the securities of our company owned by them. Under the Note Holder Voting Agreement, such stockholders may not transfer or otherwise dispose of any equity securities of our company until the earlier of: (i) the first business day following approval of the Note Holder 20% Proposal by our stockholders, (ii) the mutual written consent of the parties to the Note Holder Voting Agreement, or (iii) December 31, 2018. Such transfer restrictions do not apply to (y) the exercise of any option, warrant or other securities convertible or exchangeable for securities of our company or (z) to any transfer by the Contributor or the Contributor Parent, in each case, to any holder of a security issued by it. The Note Holder Voting Agreement also includes a power of attorney pursuant to which each stockholder designated and appointed our company and its duly authorized officers and agents as its agents and attorney in fact to act on the stockholder’s behalf to execute any proxy relating to any meeting of our stockholders for the purposes set forth in the Note Holder Voting Agreement.

On December 22, 2017, in connection with the Stock Grant Agreement, we entered into a registration rights agreement, or the Note Holder Registration Rights Agreement, with the Note Holders, pursuant to which we agreed to register the Additional Shares under the Securities Act. We agreed to file a registration statement covering the resale of the Additional Shares within 30 days of the Stock Grant Agreement and cause such registration statement to be declared effective under the Securities Act as soon as possible but, in any event, no later than 120 days following the filing date if such registration statement is filed on Form 10-K. WeS-3 or 150 days if such registration statement is filed on Form S-1. If such registration statement is not filed or declared effective by the SEC on or prior to such dates, or if after such registration statement is declared effective, without regard for the reason thereunder or efforts therefor, such registration statement ceases for any reason to be effective for more than an aggregate of 30 trading days during any 12-month period, which need not be consecutive, then in addition to any other rights the Note Holders may have under the Note Holder Registration Rights Agreement or under applicable law, we are required to pay to each Note Holder an amount in cash, as partial liquidated damages and not as a penalty, equal to 1.0% of the product obtained by multiplying (x) $1.00 by (y) the number of shares of common stock held by the Note Holder included in the registration statement (such product referred to as the Note Holder Investment Amount); provided that, in no event will we be liable for liquidated damages in excess of 1.0% of the Note Holder Investment Amount in any single month and that the maximum aggregate liquidated damages payable to the Note Holders under the Note Holder Registration Rights Agreement shall be ten percent (10%) of the Note Holder Investment Amount. The registration rights provision contained in the Payout Notes was incorporated by reference into the Note Holder Registration Rights Agreement, except that the Note Holders waived the breach by our company for failure to timely file the First Registration Statement and agreed that they are not under any obligation, and we expressly disclaim any obligation,entitled to update or alter any forward-looking statements, whetherliquidated damages as a result of new information, future eventssuch failure. Under the Note Holder Registration Rights Agreement, the Note Holders are entitled to liquidated damages if the First Registration Statement is not declared effective within 120 days following the date of the Payout Notes, but the Note Holders subsequently agreed to waive their rights to such liquidated damages until April 20, 2018. On January 23, 2018, we filed a registration statement on Form S-3 for the Additional Shares. The Note Holders waived their rights to liquidated damages in connection with the late filing of such registration statement and in connection with the effectiveness deadline for such registration statement until April 20, 2018.


Pursuant to the Stock Grant Agreement, Dr. Dolev Rafaeli and Dennis M. McGrath agreed to resign from our Board of Directors effective upon the last to occur of (i) receipt of all of the Payout Shares and all of the Additional Shares, (ii) receipt of all of the Cash Payments (either in accordance with the schedule provided in the Stock Grant Agreement or, otherwise. All subsequent forward-looking statements attributableat our option, in one lump sum on an accelerated basis), and (ii) the date that the Payout Shares and the Additional Shares have been registered for re-sale in accordance with the Note Holder Registration Rights Agreement.

Private Placement

On December 22, 2017, we entered into a securities purchase agreement, or the Purchase Agreement, with Opportunity Fund I-SS, LLC, a Delaware limited liability company, or OFI, under which OFI may invest up to $15 million in our company in a series of closings, in exchange for which OFI will receive shares of our newly designated Series B Preferred Stock at a purchase price of $1.00 per share.

On December 22, 2017, we completed the first closing under the Purchase Agreement, pursuant to which OFI provided $1.5 million to us in exchange for 1,500,000 shares of Series B Preferred Stock. On January 24, 2018, we completed a second closing under the Purchase Agreement, pursuant to which OFI provided approximately $2.2 million to us in exchange for 2,225,000 shares of Series B Preferred Stock. Under the Purchase Agreement, OFI may, but is not obligated to, make additional investments in one or more subsequent closings until an aggregate amount of $15 million has been invested or the Purchase Agreement has been terminated in accordance with its terms.

Under the Purchase Agreement, the proceeds from the first closing were to be used for working capital and general corporate purposes, the proceeds from the second closing were to be used to perform due diligence and invest in Income Generating Properties (as defined in the Purchase Agreement) that have been approved by our company’s Board of Directors, and proceeds from subsequent closings were to be used to invest in Income Generating Properties (as defined in the Purchase Agreement) that have been approved by our Board of Directors or as otherwise agreed to between us and OFI in writing prior to such subsequent closings. On March 16, 2018, we and OFI entered into a letter agreement, pursuant to which OFI agreed that we may use all proceeds for the purposes and uses described in a budget agreed to between us and OFI at the time the letter agreement was signed. In connection with such letter agreement, we agreed to provide OFI, on a quarterly basis, on or prior to 15 days after the end of each quarter, a report that describes, in reasonable detail, the actual expenses incurred, and payments made during such period compared to the expenses and payments specified in the budget for such period, certified by our Chief Financial Officer.

The terms of the Series B Preferred Stock are governed by a certificate of designation, or the Series B Certificate of Designation, filed by the Company with the Nevada Secretary of State on December 22, 2017. Pursuant to the Series B Certificate of Designation, we designated 15,000,000 shares of our preferred stock as Series B Preferred Stock. Following is a summary of the material terms of the Series B Preferred Stock:

Dividends. Holders of shares of Series B Preferred Stock shall receive cumulative dividends, pro rata among such holders, prior to and in preference to any dividend on our outstanding common stock at the per annum rate of 8% of the Series B Original Issue Price (as defined below). Dividends on each share of Series B Preferred Stock will accrue daily and be cumulative from December 22, 2017 (which we refer to as the Series B Original Issue Date) and shall be payable upon the occurrence of any voluntary or involuntary liquidation, dissolution or winding up of the Company (which we refer to as a Liquidation Event), a conversion or a redemption. The “Series B Original Issue Price” shall mean $1.00 per share, subject to appropriate adjustment in the event of any stock dividend, stock split, combination or other similar recapitalization with respect to the Series B Preferred Stock. Holders shall also be entitled to receive dividends on shares of Series B Preferred Stock equal (on an as-if-converted-to-common-stock basis regardless of whether the Series B Preferred Stock is then convertible or otherwise subject to conversion limitations) to and in the same form as dividends actually paid on shares of our common stock when, as and if such dividends are paid on shares of the common stock.


Liquidation. In the event of (i) a Liquidation Event or (ii) a merger or consolidation (other than one in which our stockholders own a majority by voting power of the outstanding shares of the surviving or acquiring corporation) or a sale, lease, transfer, exclusive license or other disposition of all or substantially all of our assets (we refer to any such event as a Deemed Liquidation Event), the holders of shares of Series B Preferred Stock then outstanding shall be entitled to be paid out of our assets available for distribution to stockholders before any payment shall be made to the holders of our common stock, Series A Convertible Preferred Stock or any other class of securities authorized that is specifically designated as junior to the Series B Preferred Stock (referred to herein as Junior Securities) by reason of their ownership thereof, butpari passu with the holders of shares of any class of securities authorized that is specifically designated aspari passu with the Series B Preferred Stock (referred to herein as the Parity Securities) on a pro rata basis, an amount per share equal to the Series B Original Issue Price, plus any accrued dividends thereon. If upon any such Liquidation Event or Deemed Liquidation Event, our assets available for distribution to stockholders shall be insufficient to pay the holders of shares of Series B Preferred Stock the full amount to which they shall be entitled and the holders of Parity Securities the full amount to which they shall be entitled, the holders of shares of Series B Preferred Stock and the holders of shares of Parity Securities shall share ratably in any distribution of the assets available for distribution in proportion to the respective amounts which would otherwise be payable in respect of the shares held by them upon such distribution if all amounts payable on or with respect to such shares were paid in full. Upon a Liquidation Event or a Deemed Liquidation Event, in the event that following the payment of such liquidation preference we shall have additional cash and other assets available for distribution to stockholders, then the holders of shares of Series B Preferred Stock shall participatepari passu with the holders of shares of Parity Securities and Junior Securities based on the then current conversion rate (disregarding for such purposes any conversion limitations) with respect to all remaining distributions, dividends or other payments of cash, shares or other assets and property of our company, if any.

Voting Rights. On any matter presented to our stockholders for their action or consideration, each holder of Series B Preferred Stock shall be entitled to cast the number of votes equal to the number of whole shares of common stock into which the shares of Series B Preferred Stock held by such holder are convertible as of the record date for determining stockholders entitled to vote on such matter (subject to the conversion limitations described below). Except as provided by law or by the other provisions of the Series B Certificate of Designation, the holders shall vote together with the holders of shares of common stock as a single class. However, as long as any shares of Series B Preferred Stock are outstanding, we shall not, without the affirmative vote of the holders of a majority of the outstanding shares of Series B Preferred Stock, or the Requisite Holders, (i) issue any class of equity securities that is senior in rights to the Series B Preferred Stock, (ii) issue any Parity Securities, (iii) alter or change adversely the powers, preferences or rights given to the Series B Preferred Stock or alter or amend the Series B Certificate of Designation, (iv) amend our articles of incorporation or other charter documents in any manner that adversely affects any rights of the holders of Series B Preferred Stock, (v) except pursuant to the redemption provisions of Parity Securities, redeem any shares of our preferred stock or common stock (other than pursuant to employee or consultant agreements giving us the right to repurchase shares at the original cost thereof upon the termination of services and provided that such repurchase is approved by our Board of Directors), or (vi) enter into any agreement with respect to any of the foregoing.

Conversion. Each share of Series B Preferred Stock plus accrued, but unpaid, dividends thereon, or the Aggregate Preference Amount, shall be convertible, at any time and from time to time at the option of the holder thereof, into that number of shares of common stock determined by a formula (computed on the date of conversion), (i) the numerator of which is equal to the Aggregate Preference Amount and (ii) the denominator of which is equal to the quotient of the Conversion Price divided by $1.33. The “Conversion Price” for the Series B Preferred Stock shall initially be equal to $0.8684, subject to adjustment as described in the Series B Certificate of Designation. In addition, upon the earlier to occur of: (i) a Deemed Liquidation Event or (ii) if there has not been a breach or default by us under the Purchase Agreement that has occurred and is continuing, May 31, 2018, each share of Series B Preferred Stock plus accrued, but unpaid, dividends thereon shall be automatically converted into that number of shares of common stock determined by dividing $1.33 by the Conversion Price. Notwithstanding the forgoing, if we have not obtained approval from our stockholders with respect to the issuance of shares upon conversion in excess of 19.99% of the issued and outstanding common stock on the applicable conversion date (which we refer to as the Stockholder Approval), then we may not issue, upon conversion of the Series B Preferred Stock, a number of shares of common stock which, when aggregated with any shares of common stock issued on or after the Series B Original Issue Date and prior to such conversion date, would exceed 19.99% of the issued and outstanding shares of common stock (subject to adjustment for forward and reverse stock splits, recapitalizations and the like) (we refer to such number of shares as the Issuable Maximum). Each holder shall be entitled to a portion of the Issuable Maximum equal to the quotient obtained by dividing (i) the Series B Original Issue Price of such holder’s Series B Preferred Stock by (ii) the aggregate Series B Original Issue Price of all Series B Preferred Stock issued to all holders.


Redemption. If (i) there is a breach by us of any of our representations and warranties contained in Sections 3.1(a) (Subsidiaries), 3.1(b) (Organization and Qualification), 3.1(c) (Authorization; Enforcement), 3.1(d) (No Conflicts), 3.1(f) (Issuance of the Shares), 3.1(g) (Capitalization), or 3.1(n) (Taxes) of the Purchase Agreement that has not been cured within 30 days after the date of such breach or (ii) Stockholder Approval has not been obtained by March 31, 2018 (each event being referred to herein as a Redemption Event), then each holder of Series B Preferred Stock may, at its option, require us to redeem any or all of the shares of Series B Preferred Stock held by such holder at a price per share equal to $1.33, plus accrued, but unpaid, dividends through and including the date of such redemption. We must provide a notice, or an Event Notice, to each holder of the occurrence of a Redemption Event of the kind described in (i) above (referred to herein as a Breach Event) as soon as practicable after becoming aware of such Breach Event, but in any event, not later than fifteen (15) days after such Breach Event and such notice shall provide a reasonable description of such Breach Event. A holder must send written notice of redemption, or a Redemption Notice, to us within ninety (90) days after (i) we provide such holder an Event Notice with respect to a Breach Event or (ii) the occurrence of a Redemption Event of the kind described in (ii) above. For the avoidance of doubt, if we do not timely provide an Event Notice, the holder shall nevertheless have the right to deliver a Redemption Notice in connection with any Redemption Event. If a holder fails to send a Redemption Notice on or prior to the 90th day after the occurrence of any Redemption Event, then such holder will lose such holder’s right to redemption with respect to the particular Redemption Event, but not any other Redemption Event. We did not obtain Stockholder Approval prior to March 31, 2018.

The Purchase Agreement is subject to the usual pre- and post-closing representations, warranties and covenants. In addition, we agreed that, so long as the shares of Series B Preferred Stock purchased by OFI are outstanding, our debt (as defined by U.S. generally accepted accounting principles, or GAAP) shall not exceed 45% of our fixed assets without the prior written consent of the Requisite Holders. Subject to stockholder approval, we also agreed to amend the certificate of designation for our Series A Convertible Preferred Stock to change the conversion price from $2.5183 to $1.12024021352 such that each share of Series A Convertible Preferred Stock will be initially convertible into 56.20 shares of common stock instead of 25 shares of common stock. In addition, we agreed that at any time prior to the termination of the OFI Voting Agreement (as defined below), we shall cause any person who acquires any securities from us or any of our affiliates that, together with all securities held by such acquirer and its affiliates, will own, directly or indirectly, five percent (5%) or more of our outstanding common stock (after giving effect to the right of any such person to convert or exchange securities), to become a party to the OFI Voting Agreement by causing such person, as a condition to the delivery of such securities, to sign a counterpart signature page thereto that joins such person to the OFI Voting Agreement.

We also agreed to nominate two (2) directors to our Board of Directors upon request of OFI. In furtherance thereof, on December 22, 2017, Messrs. Suneet Singal and Darrel C. Menthe delivered resignation letters to our Board of Directors pursuant to which they resigned from the Board of Directors effective automatically on the third (3rd) day following written request to do so from OFI. Notwithstanding the fact that OFI has not yet requested Messrs. Singal and Menthe to resign from our Board of Directors, Messrs. Singal and Menthe did resign on March 3, 2018. Their resignations were not in connection with any known disagreement with the Company.

As promptly as possible following the first closing, we are also required to file a proxy statement and hold a special meeting of our stockholders to authorize and approve the issuance of shares of common stock upon conversion of the Series B Preferred Stock and the amendment to the certificate of designation for our Series A Convertible Preferred Stock described above. As of the date of this report, we have not yet filed such proxy statement.

In furtherance of obtaining such stockholder approval, on December 22, 2017, OFI entered into a shareholder voting support and confidentiality agreement, or the OFI Voting Agreement, with the Contributor and certain other significant stockholders of our company, including the Note Holders, pursuant to which the such stockholders agreed to vote their shares in favor of the transactions contemplated by the Purchase Agreement, including the issuance to OFI or its designees of common stock upon conversion of its Series B Preferred Stock equal to 20% or more of the common stock or 20% or more of the voting power outstanding before the issuance (which we refer to as the OFI 20% Proposal), and also agreed to certain transfer restrictions on the securities of our company owned by them. Under the OFI Voting Agreement, such stockholders may not transfer or otherwise dispose of any equity securities of our company until the earlier of: (i) the date of termination of the Purchase Agreement in accordance with its terms; (ii) the later of (a) the date that this registration statement becomes effective or (b) the first business day following approval of the OFI 20% Proposal by our stockholders, (iii) the mutual written consent of the parties to the OFI Voting Agreement, or (iv) December 31, 2018. Such transfer restrictions do not apply to the exercise of any option, warrant or other securities convertible or exchangeable for securities of our company, or following stockholder approval of the OFI 20% Proposal, to the following transfers: (i) if the stockholder is a corporation, partnership, limited liability company or other entity, any transfer to an affiliate if such transfer is not for value; or (ii) if the stockholder is an individual, transfers, (a) for nominal consideration or as a gift to any person acting on its behalf are expresslymember of such stockholder’s immediate family (defined as the spouse, parents, lineal descendants, the spouse of any lineal descendant, and brothers and sisters) or a trust for the benefit of such stockholder or any member of such stockholder’s immediate family, (b) in connection with estate or tax planning, (c) to non-profit organizations qualified in their entiretyas charitable organizations under Section 501(c)(3) of the Internal Revenue Code of 1986, as amended, or (d) upon the death of such stockholder pursuant to a will or other instrument taking effect upon the death of such stockholder, or pursuant to the applicable laws of descent and distribution to such stockholder’s estate, heirs or distributes. The restrictions also do not apply to any transfer by the cautionary statements containedContributor or the Contributor Parent, in each case, to any holder of a security issued by it. The OFI Voting Agreement also includes a power of attorney pursuant to which each stockholder designated and appointed our company and its duly authorized officers and agents as its agents and attorney in fact to act on the stockholder’s behalf to execute any proxy relating to any meeting of our stockholders for the purposes set forth in the OFI Voting Agreement.


As a condition to the first closing, we entered into a registration rights agreement, or the OFI Registration Rights Agreement, with OFI, pursuant to which we agreed to register all shares of common stock that may be issued upon conversion of the Series B Preferred Stock, or the Registrable Securities, under the Securities Act. We agreed to file a registration statement covering the resale of such Registrable Securities within 30 days of the first closing and cause such registration statement to be declared effective under the Securities Act as soon as possible but, in any event, no later than 120 days following the filing date if such registration statement is filed on Form S-3 or 150 days if such registration statement is filed on Form S-1. If such registration statement is not filed or declared effective by the SEC on or prior to such dates, or if after such registration statement is declared effective, without regard for the reason thereunder or efforts therefor, such registration statement ceases for any reason to be effective for more than an aggregate of 30 trading days during any 12-month period, which need not be consecutive, then in addition to any other rights the holders of Series B Preferred Stock may have under the OFI Registration Rights Agreement or under applicable law, we shall pay to each holder an amount in cash, as partial liquidated damages and not as a penalty, equal to 1.0% of the product obtained by multiplying (x) the Series B Original Issue Price by (y) the number of shares of Registrable Securities held by the holder (such product referred to herein as the Investment Amount); provided that, in no event will we be liable for liquidated damages in excess of 1.0% of the Investment Amount in any single month and that the maximum aggregate liquidated damages payable to the holders under the OFI Registration Rights Agreement shall be ten percent (10%) of the Investment Amount. On January 23, 2018, we filed a registration statement on Form S-3 to register the shares issued to OFI in the first closing. OFI waived its right to liquidated damages in connection with the late filing of such registration statement.

Under the Purchase Agreement, we also agreed to indemnify and hold OFI and its successors and permitted assignees (collectively referred to herein as the Investor Indemnified Parties) harmless from, any and all Damages (as defined below) incurred or suffered by such Investor Indemnified Party arising out of any inaccuracy or other breach of any representation or warranty of our company in any of the Transaction Documents (as defined in the Purchase Agreement) or any breach of covenant or agreement made by us in any of the Transaction Documents. “Damages” means the amount of (i) the sum of the aggregate amount of all damages, losses, liabilities and expenses (including reasonable expenses of investigation and reasonable attorneys’ fees and expenses) in connection with any action, suit or proceeding whether involving a third party claim or a claim solely between the parties, but excluding any incidental, indirect or consequential damages, losses, liabilities or expenses; (ii) multiplied by the Indemnity Gross Up Factor. The “Indemnity Gross Up Factor” is equal to X divided by Y, where X is equal to 1 and Y is equal to 1 minus a fraction, the numerator of which is equal to the number of shares of common stock held by OFI, determined and on a fully diluted basis assuming the full conversion of shares of Series B Preferred Stock that OFI is then entitled to convert; and the denominator of which is the number of shares of common stock determined on a fully diluted basis. Notwithstanding the foregoing, no Investor Indemnified Party shall be entitled to indemnification unless and until the aggregate Damages incurred in respect of all claims collectively exceeds $50,000 whereupon Investor Indemnified Parties shall only be entitled to indemnification for all such Damages in excess of such $50,000 threshold.

The Purchase Agreement may be terminated by the written agreement of us and OFI, or by us or OFI if the final closing does not take place prior to December 31, 2018.

Our Prior Business Operations

Under its previous name, PhotoMedex, Inc., our company was, until the recent sale of the last significant business unit (its consumer products division which was sold to ICTV Brands, Inc., or ICTV, on January 23, 2017; see Note 2, Discontinued Operations, to our consolidated financial statements), as described below and in other sections of this section.

PART I
Item 1.
Business
Our Company
PhotoMedex, Inc., re-incorporated in Nevada December 30, 2010, originally formed in Delaware in 1980, isreport, a Global Skin Health products and services company providing integrated disease management and aesthetic solutions to dermatologists, professional aestheticians and consumers. We provideprovided proprietary products and services that addressaddressed skin diseases and conditions including psoriasis, vitiligo, acne, actinic keratosis (a precursor to certain types of skin cancer), photo damage and photo damage. Our experienceunwanted hair.


Before we commenced our current real estate business, we organized our business into three operating segments based upon our management structure, products and services offered, markets served and types of customers, as follows: The Consumer segment (sold to ICTV on January 23, 2017) derived its revenues from the design, development, manufacturing and selling of long-term hair reduction and acne consumer products. The Physician Recurring segment derived its revenues from the XTRAC (sold to MELA Sciences on June 22, 2015) procedures performed by dermatologists, the sales of skincare products (sold to Pharma Cosmetics on September 15, 2016), the sales of surgical disposables and accessories to hospitals and surgery centers (sold to Dalian JiKang Medical Systems September 1, 2015) and on the repair, maintenance and replacement parts on various products. The Professional segment generated revenues from the sale of equipment, such as lasers, medical and esthetic light and heat based products and LED products.

We still market and sell our LHE® brand products, which were included in the physician market provides the platform to expand our skin health solutions to spa markets, as well as traditional retail, online and infomercial outlets for home-use products. ThroughProfessional segment, through our subsidiary, Radiancy, Inc., which was merged into PhotoMedex in 2011, we've added a range of home-use devices under the no!no!® brand, for various indications including hair removal, acne treatment, skin rejuvenation, and lower back pain. In addition, our professional product

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line increased its offerings for acne clearance, skin tightening, psoriasis care and hair removal sold to physician clinics and spas.
On May 12, 2014, PhotoMedex, Inc. acquired 100% of the shares of LCA-Vision Inc., a Delaware corporation ("LCA-Vision" or "LCA"). LCA is a provider of fixed-site laser vision corrections services at its LasikPlus® vision centers. The results of operations of LCA-Vision have been included from May 13, 2014 through December 31, 2014Radiancy. We are in the consolidated financial statements. PhotoMedex subsequently sold LCA on January 31, 2015. See Discontinued Operations below.
Also on May 12, 2014, PhotoMedex entered into an $85 million senior secured credit facilities ("process of liquidating the Facilities") with JP Morgan Chase ("Chase") which included a $10 million revolving credit facilityremaining legacy inventory and a $75 million four-year term loan. The facilities were utilized to refinance the existing term debt with Chase, fund the acquisition of LCA and for working capital and other general corporate purposes. Interest is determined at Eurodollar plus a margin between 3.25% and 4.50%. The margin is updated quarterly based on the then-current leverage ratio. The facilities are secured by a first priority security interest in and lien on all assets of the Company. All current and future subsidiaries are guarantors on the facilities.
There are financial covenants including a maximum leverage covenant and a minimum fixed charge covenant,this business line, after which the Company must maintain. These covenants are determinedquarterly based on a rolling past four quarters of financial data. As of June 30, 2014 the Company failed to meet the financial covenants and as of December 31, 2014, the Company continued to fail to meet these covenants and remains in default.
On August 4, 2014, the Company received a notice of default and a reservation of rights from Chase and engaged a third-party independent advisor to assist the Company in negotiating a longer term solution to the defaults. The parties had entered into an initial Forbearance Agreement (the "Initial Forbearance Agreement") on August 25, 2014. On November 4, 2014, the Company entered into an Amended and Restated Forbearance Agreement (the "Amended Forbearance Agreement") with the lenders that are parties to the Credit Agreement and with Chase, as Administrative Agent for the Lenders.
Effective February 28, 2015, the Company entered into a Second Amended and Restated Forbearance Agreement (the "Second Amended Forbearance Agreement") with the lenders (the "Lenders") that are parties to the Credit Agreement dated May 12, 2014, and with JP Morgan Chase, as Administrative Agent for the Lenders.
Pursuant to the terms of the Second Amended Forbearance Agreement, the Lenders have agreed to forbear from exercising their rights and remedies with respect to the Specified Events of Default from August 25, 2014 until April 1, 2016, or earlier if an event of default occurs (the "Forbearance Period"). Chase and the Lenders agreed that the Company shall not be obligated to pay the principal amounts set forth in Section 2.08(b) of the Credit Agreement for any date identified therein during the period beginning on February 28, 2015 and ending on the end of the Forbearance Period (the "Effective Period") and that any failure to do so shall not constitute a default or event of default. Instead, the Lenders and the Company agreed that the Company would make prepayments against the Term Loan of $250,000 on the first business day of each month during the Forbearance Period, which will be applied in direct order of maturity. The Company also agreed that, on or before the fifth calendar day of each month, the Company would pay against the Term Loan $125,000 to the extent that the cash-on-hand exceeds $5 million, and 100% of the cash-on-hand in excess of $7 million, also to be applied to the Term Loan in inverse order of maturity.
Under the provisions of the Second Amended Forbearance Agreement, the Company will not have to comply with certain financial covenants contained in Section 6.11 of the Credit Agreement for the Forbearance Period, and that any failure to do so shall not constitute a default or event of default. However, the Company will have to meet certain minimum EBITDA targets (as defined in the forbearance agreement) for the quarters ending March 31, 2015, June 30, 2015, September 30, 2015 and December 31, 2015.
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Pursuant to the Second Amended Forbearance Agreement, all loans under the Facilities shall, beginning November 1, 2014, bear interest at the CB Floating Rate (as defined in the Credit Agreement) plus 4.00%. Additionally, following the occurrence and continuance of any default or event of default (other than a Specified Event of Default), the Company's obligations under the Facilities shall, at the option of Chase and the Lenders, bear interest at the rate of 2.00% plus the rate otherwise in effect.
The Company and its subsidiaries have also agreed not to pay in cash any compensation to the either the Company's Chief Executive Officer or President that is based on a percentage of sales or another metric other than those officers' base salary, perquisites and standard benefits provided to or on behalf of those executives under the terms of their employment agreements. Those payments may be accrued or deferred and paid in cash only after the repayment of the Facilities in full.
The Company has agreed to provide, on or before May 29, 2015, a strategic business plan for the overall direction of the Company's and its subsidiaries' businesses, including projected income statements, balance sheets, schedules of cash receipts and cash disbursements, payments and month-end balances, and detailed notes and assumptions, projected on a monthly basis through April 1, 2016. The Company has also agreed to provide quarterly updates to that plan by August 31, 2015, November 30, 2015 and February 29, 2016.
The Company continues to retain the services of both Getzler Henrich & Assoc. LLC, a third-party independent business advisor, as well as Canaccord Genuity, Inc., a banking and financial services company, and has also retained the services of Nomura Securities International, Inc., also a banking and financial services company. During the Forbearance Agreement, the Company and these advisors will continue to prepare and distribute offering memoranda and other marketing materials to prospective lenders with regard to a proposed credit facility for the Company, the proceeds of which would be in an amount sufficient to repay in full and in cash the Company's remaining obligations under the Facilities, and to explore other strategic alternatives. The closing of any such refinancing or alternative arrangement would occur no later than the end of the Forbearance Period.
The Company agreed to limit certain capital expenditures to $100,000 per quarter, except for those involving the Company's XTRAC® or VTRAC® medical devices, and will not make investments or acquire any other interests in affiliated companies except as agreed to by the Lenders.
As consideration for the Lender's entry into the Second Amended Forbearance Agreement, the Company has agreed to pay the Lenders certain forbearance fees (the "Forbearance Fees"), which are earned on the last business day of each of the specified months: for May and June 2015, $750,000 each month; for July through September 2015, $1,000,000 each month; for October through December 2015, $1,250,000 each month; and for January through March 2016, $1,500,000 each month. The fees are due in full upon the completion of the forbearance period. However, should the Company complete a capital transaction acceptable to the Lenders that reduces the then-outstanding principal balance of the Term Loan to less than $10 million and repays all Forbearance Fees accrued and unpaid to that date, the monthly Forbearance Fee for the remainder of the Forbearance Period shall be earned and accrued in an amount that is 50% of the amount specified for each of the remaining months. In addition, the $500,000 Forbearance Fee set forth in Section 4.10(b) of the Amended Forbearance Agreement remains due and payable to the Lenders on the earlier of the Expiration Date or the Termination Date of the Forbearance Period.  All Forbearance Fees are considered earned and are included in the Obligations under the Credit Agreement.
The Second Amended Forbearance Agreement is also subject to customary covenants, including limitations on the incurrence of or payments on indebtedness to other persons or entities and requirements that the Company provide periodic financial information and information regarding the status of outstanding litigation involving the Company and its subsidiaries to the Lenders.
On March 3, 2014, PhotoMedex' wholly-owned subsidiary, Radiancy, Inc., formed a wholly-owned subsidiary in Hong Kong, Radiancy (HK) Limited, through which we have started to directly market certain products and services to patients and consumers in selected markets in that region.
On March 5, 2014, PhotoMedex formed a wholly-owned subsidiary in India, PhotoMedex India Private Limited, through which we plan to directly market certain products and services to patients and consumers in selected markets in that country.
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On August 18, 2014, the Company formed a wholly-owned subsidiary in Korea, PhotoMedex Korea Limited, through which we plan to directly market certain products and services to patients and consumers in selected markets in that country.
Discontinued Operations
As stated above, on May 12, 2014, the Company acquired LCA. See Our Company.
LCA is a provider of fixed-site laser vision corrections services at its LasikPlus® vision centers. This business, from May 2014 through December 31, 2014, was a fourth business segment for the Company, referred to as the Clinics Segment. Through this segment:
We provided fixed-site laser vision correction services at our LasikPlus® vision centers. Our vision centers provided the staff, facilities, equipment and support services for performing laser vision correction that employ advanced laser technologies to help correct nearsightedness, farsightedness and astigmatism. Our vision centers were supported by independent ophthalmologists and credentialed optometrists, as well as other healthcare professionals. The ophthalmologists perform the laser vision correction procedures in our vision centers, and ophthalmologists or optometrists conduct pre-procedure evaluations and post-operative follow-up care in-center. Most of our patients receive a procedure called laser-assisted in situ keratomileusis ("LASIK"), which we began performing in the United States in 1996.
As of December 31, 2014, we operated 59 LasikPlus fixed-site laser vision correction centers, generally located in metropolitan markets in the United States consisting of 51 full-service LasikPlus fixed-site laser vision correction centers and nine pre- and post-operative LasikPlus satellite vision centers. Included in the 51 full-service vision centers were four vision centers owned and operated by ophthalmologists who license our trademarks.
The main product line through LCA was Laser vision correction procedures that reshape the cornea with an excimer laser to correct refractive vision errors by changing the curvature of the cornea. These procedures may reduce the need for wearing corrective lenses such as glasses and contact lenses. Our doctors make an assessment of a patient's candidacy for laser vision correction and determine the correction required to program the excimer laser. The software of the excimer laser then calculates the number and pattern of pulses needed to achieve the intended correction using a specially developed algorithm. The typical laser vision correction procedure takes approximately 15 – 20 minutes to complete. The eye is anesthetized using topical eye drops. The patient reclines under the laser, a lid speculum holds the eyelids open, and the patient focuses on a blinking fixation light while the excimer laser pulses are applied. The excimer laser is a high-energy ultraviolet "cold" laser, meaning that no heat is generated. This non-thermal ablation permits precise reshaping of the cornea. The amount of tissue ablated and the ablation pattern depend upon the refractive error being corrected. Shortly after the procedure, the patient leaves the laser vision center with instructions to rest the remainder of the day. Follow-up visits with an optometrist or ophthalmologist are typically scheduled for one day, one week and one to three months post-procedure.
LASIK
In 1995, LCA began performing laser vision correction, including LASIK which continues to account for the majority of the laser vision correction procedures performed in the United States. In LASIK procedures, our surgeons use a femtosecond laser to create a thin flap in the cornea, which remains hinged to the eye. The surgeon then lays back this corneal flap and applies excimer laser pulses to the exposed surface of the cornea to treat the eye according to the patient's prescription. The surgeon then folds the corneal flap back to its original position and inspects it to ensure that it remains secured in position by the natural suction of the cornea. Because the surface layer of the cornea remains intact with LASIK, a bandage contact lens is normally not required and the patient typically experiences little discomfort. LASIK often has the advantage of more rapid recovery than Photorefractive Keratectomy ("PRK"), with most patients seeing well enough to drive a car the next day. The LASIK procedure generally allows an ophthalmologist to treat both eyes of a patient during the same visit.
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PRK
In PRK procedures, the ophthalmologist removes the thin layer of cells covering the outer surface of the cornea (the epithelium) in order to apply the excimer laser pulses directly to the surface of the cornea. Following the PRK procedure, the ophthalmologist places a bandage contact lens on the eye to protect it. The patient may experience discomfort and blurred vision until the epithelium heals, which can take several days. The doctor generally will prescribe certain topical pharmaceuticals for use by the patient post-procedure to assist in alleviating discomfort, minimizing infection and helping to promote corneal healing. Although a patient generally experiences substantial improvement in clarity of vision within a few days following the procedure, it can take several months for the full benefits of the PRK procedure to be realized. Some patients elect to have one eye treated in one visit and the second eye treated at a later date.
LASIK and PRK procedures are performed using the same excimer lasers and offer the same results after healing occurs. Each has its advantages. Based on the pre-procedure examination and assessment, our doctors determine which laser correction procedure is best for each patient.
For the LCA-Vision business, we faced competition as laser vision correction, whether performed at one of our vision centers or elsewhere, is an alternative to other surgical as well as non-surgical treatments to correct refractive vision disorders. These non-surgical treatments include eyeglasses and contact lenses. Other refractive surgery procedures include refractive lens exchange and ICL.
We also faced competition from other providers of laser vision correction. A fragmented system of local providers, including individual or small groups of opticians, optometrists and ophthalmologists, and chains of retail optical stores and multi-site eye care vision centers deliver eye care services in the United States. Industry sources estimate that local ophthalmologists and hospitals service approximately 70% of the laser vision correction market. Corporate laser vision correction providers, such as LasikPlus®, are a specialized type of provider, operating multi-site eye care centers that provide primarily laser vision correction.
The LCA headquarters and one of the laser vision correction centers are located in an office building that we owned in Cincinnati, Ohio, which contains approximately 30,000 square feet. The other laser vision correction centers and our corporate data center were in leased locations. The typical vision center location is in a professional office building or retail site and includes a laser surgery room, private examination rooms and patient waiting areas. Vision centers range in size from approximately 2,400 to 6,100 square feet with lease expiration dates through September 30, 2021.
After preliminary investigations and discussions, the Board of Directors of the Company, with the aid of its investment banker, decided to enter into, substantive, confidential discussions with potential third-party buyers and began to develop plans for implementing a disposal of the assets and operations of the business. Effective January 31, 2015, PhotoMedex and LCA entered into a Stock Purchase Agreement (the "Stock Purchase Agreement") with Vision Acquisition, LLC ("Vision"), under which Vision acquired LCA and its subsidiaries from PhotoMedex for a total purchase price of $40 million in cash (the "Purchase Price"). After giving effect to working capital and indebtedness adjustments and the payment of professional fees, the Company realized net proceeds of approximately $36.5 million from this sale, of which $2 million was placed in escrow. Pursuant to the Termination of Joinder, dated as of January 31, 2015, LCA has been released from all of its obligations, including its guarantee and collateral obligations, in connection with the Facilities. The Company has used the proceeds from this transaction to pay down portions of its outstanding revolving line of credit and term loan under the Credit Agreement. As a result of that transaction, PhotoMedex's creditors agreed to waive certain prepayments set for February 1st and February 15th.
Based on the above information, the Company accordingly classified this former segment as held for sale and discontinued operations in accordance with ASC Topic 360.The results of operations of LCA-Vision have been included from May 13, 2014 through December 31, 2014 in the consolidated financial statements as assets and liabilities held for sale as of the balance sheet date. For the statement of operations, the activity related to LCA is captured as discontinued operations.
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Our Key Strategies
Our technologies, products and research efforts are directed to addressing a worldwide aesthetic industry valued at $34 billion annually. We provide dermatologists, professional aestheticians, and consumers with the equipment and skin care products they need to treat psoriasis, vitiligo, acne, and UV damage, among other skin conditions. In December 2011, PhotoMedex merged with Radiancy Inc. which brought to PhotoMedex the no!no!® line of home-use consumer products for hair removal, acne treatment, skin rejuvenation and lower back pain. Radiancy also markets capital equipment to physicians, salons and med spas for hair removal, acne treatment, skin tightening and rejuvenation and psoriasis care. In addition to a synergistic product line, Radiancy possesses a proprietary consumer marketing engine built upon direct-to-consumer sales and creative marketing programs that drive brand awareness. During 2013 and throughout 2014, we began to benefit from the impact of these marketing methodologies and expertise on our XTRAC® Excimer Laser and NEOVA® topical skin care lines while continuing to realize organic and geographic growth of additional brands.
Skilled Direct Sales Force to Target Physician and Professional Segments
PhotoMedex has long been active in physician sales, having developed a portfolio of medical devices and topical formulations that are provided under various financial arrangements primarily to dermatologists and plastic surgeons as well as other aesthetic professionals at salons and med spas. These products comprise medical lasers for skin diseases such as psoriasis and vitiligo, phototherapies for acne and sun damage, therapeutic skin care and surgical laser systems, among other products. One of our competitive advantages is an experienced, 44-person, physician-targeted sales force that is currently selling into 3,000 U.S. locations. We are focused on capitalizing on this skilled sales force in order to drive greater adoption of our line of proprietary products. These products provide skin rejuvenation, acne treatment, hair removal and other services for dermatologists and med spas
Expertise in Global Consumer Marketing
We have a highly advanced consumer sales engine accompanied by creative marketing programs, well-tested and successful direct-to-consumer marketing strategies and a global distributor and retail network. The no!no!® products are sold at roughly 5,000 retail outlets across 55 countries, through infomercials and print, radio other television advertising worldwide, online, on home shopping channels and at stores and kiosks.
We have continued to capitalize upon our consumer marketing expertise to further patient awareness of our XTRAC® Excimer Laser and NEOVA® topical skin care products, which have traditionally been marketed only to physicians and aesthetic professionals. By incorporating a direct-to-consumer/patient element, we have increased brand awareness and direct patients into physicians' practices in search of these products. Our experience in effectively penetrating culturally distinct regions with targeted advertising is also anticipated to further benefit the expansion of our non-device technologies into global consumer channels.
Corporate Cultures and Clinical Excellence
We believe that the combination of our consumer and physician businesses will enable a revenue and earnings growth potential that neither firm would have been able to achieve independently. Beyond these benefits, we have also developed complementary corporate cultures, with shared commitments to innovation, product quality and a high level of customer service to address the evolving needs of customers. We also emphasize the development of products and technologies that are backed by science and clinical support. We hold more than 90 clearances from the U.S. Food and Drug Administration (FDA) under Section 510(k) of the Food, Drug and Cosmetic Act, indicating that we have permission to commercialize such products in the U.S. based on having submitted safety and efficacy information to the FDA. See Government Regulations – Regulations Relating to Products and Manufacturing discussion below.
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Full Product Life Cycle Model
Since 2004, we have introduced a portfolio of professional-grade consumer products for hair removal, acne treatment, skin rejuvenation, facial skin tightening and lower back pain. These products - marketed globally under the no!no!® and Kyrobak® brands - are built upon the same technology platforms that are used in medical devices for physicians and aestheticians. We have been able to bring the clinical solutions used by physicians and med spas to the consumer home-use market by successfully miniaturizing equipment into handheld or lightweight convenient-to-carry products and engaging in a multi-faceted worldwide sales and marketing strategy. Under this type of "full product life cycle model," the development of medical technology cleared through regulatory agencies, such as the FDA, and acceptance by physicians can ultimately lead to an effective new technology for consumer use.
Once a product idea is generated, it is refined and tested through the development stage, which includes leveraging the knowledge of our Scientific Advisory Board; our marketing organization then works to encourage physician adoption of the new process/product. While many companies may stop at this point, our full product life cycle encourages us to continue to innovate and broaden our market opportunity by further miniaturizing professional technologies for home-use. Optimizing technologies for consumer use involves many considerations, including understanding and matching consumer expectations and providing superior customer service, eliminating the need for consumers to calibrate or safety test devices in the way that professionals are required to do for in-office capital equipment, and setting price points that are favorable for us but affordable for consumers. These key elements were the basis for Radiancy's no!no!® product line, which received the Consumer Survey of Product Innovation's 2011 "Product of the Year" award in the At Home Beauty Treatment category and the HSN Most Innovative Product Award for 2012.
Our Global Growth Strategies
The global market for aesthetic devices and procedures continues to expand, driven by an individual desire to improve one's appearance; a higher disposable income being spent on aesthetic treatments; an aging population in the industrialized world that desires a more youthful look; a younger generation seeking preventive solutions for the inevitable aging process; technological advances making products available to a consumer market that were previously only possible at the physician level; an increasing number of conditions, including acne and wrinkles, that can now be non-invasively treated; and a lower procedural cost, which has expanded the availability and affordability of many procedures to a greater number of individuals.
We are focused on addressing the above-mentioned trends by growing and expanding our three core business segments: consumer, physician recurring and professional. We possess a solid line of technology platforms that are currently driving, and are expected to continue to drive, new product introductions and consequently greater revenues. We are focused on growth both through geographic expansion and the pursuit of additional diversified marketing initiatives that are intended to increase market share and sustain the profitability that we have reported thus far.
Our three main sources of revenue generation form our three business segments: Consumer segment, Physician Recurring segment and Professional segment. For a period of May to December 2014 we had a fourth segment of business, the Clinics segment which represented the LCA Vision business. See Discontinued Operations above. Specific growth strategies as they relate to each of these core business channels are described below.
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Consumer Segment
Expand into additional geographic markets. We intend to continue implementing a global multichannel sales and marketing strategy. We have sold more than 5 million no!no!® units to consumers, the majority of these over the past four years. Growth has been largely driven by North America (with a population of 318 million), United Kingdom (pop. 64 million), Canada (pop. 35 million) and Japan (with a population of 127 million), although our products are sold across 55 countries. During 2013 we launched our consumer marketing platform in Germany (population of approximately 81 million people) and in Brazil (population of approximately 187 million people) and more recently, in 2014, in Columbia (pop. 47 million) and Hong Kong (pop. 7 million). Our ability to grow organically is significantly dependent upon the ability to advertise our products locally in a cost effective manner and therefore subject to the volatile availability of such advertising media.
Strengthen our retail distribution channel. We intend to continue the expansion and growth of our retail presence in the US and internationally. In the US in 2013 we expanded the in-store availability of our flagship product, no!no! Hair, which is now available for sale at approximately 950 Bed Bath & Beyond stores nationwide. This adds to the Company's rapidly growing global retail footprint including more than 7,500 retail outlets worldwide.
Diversify media campaigns, extending beyond the historical overnight infomercial audience to also target short-form infomercials and daytime advertising. We will continue to diversify our media campaigns beyond the overnight infomercial audience (the 28-minute infomercial) by increasing our advertising expenditures for infomercials in short form (30 second, 1 minute, 2 minute and 5 minute) in daytime media buys. Furthermore, we continue to test and expand a variety of media messages in various formats (TV, radio, print) and in multiple languages. In addition, the Company continues to seek alternative means of reaching consumers to create awareness of our products in order to reduce its reliance on traditional television advertising, particularly aimed at offsetting the long-term trends of consumers seeking forms of entertainment that are different from historical TV broadcast and cable formats.
Capitalize on our consumer marketing expertise to bring NEOVA® and our other products into the consumer segment. With our marketing expertise, we are positioned to introduce other technologies—either via product extension from the health and wellness area of the no!no!® and Kyrobak® brands or from our NEOVA® and XTRAC® technologies – into the consumer markets
Build out brand extensions of the no!no!® and LHE and Kyrobak product lines into additional health and wellness areas. There are several additional brand extensions in the development pipeline that are in the process of being readied for launch, which could increase the growth trajectory of our existing product offerings.
Leverage technology development in the physician and professional segments to drive new products for the consumer channel. We believe that our consumer line can continue to increase market penetration. We have expertise in adapting products for consumer markets, as we have taken proprietary technologies focused toward physicians and med spas and adapted them to the home-use market and will attempt to continue to grow sales and increase gross margins in this manner.
Physician Recurring Segment
Incorporate direct-to-consumer sales strategies to educate patients about the availability of treatments for psoriasis, vitiligo and other skin care concerns and, in turn, motivate patients to seek out XTRAC® and NEOVA® technologies sold by physicians, clinicians and other aesthetic professionals. Via the reverse merger, we now have greater options to offer our physician community. We currently sell into over 3,000 physician offices. With a direct-to-patient strategy creating awareness, we believe that we can drive these revenues significantly higher given the safety and effectiveness of our technology in treating psoriasis and vitiligo compared to alternatives on the market.
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In 2012 we launched a direct to patient and physician education campaign in the US for psoriasis and vitiligo patients. The Live Clear. Live Free. campaign is designed to accelerate awareness of the XTRAC® excimer laser treatment, improve patient care, expedite information sharing, and reduce healthcare costs for what many believe is one of the most challenging skin diseases. The national and local advertising campaigns include TV, radio and direct mail marketing. 'Live Clear. Live Free.' brings PhotoMedex's support of practices that administer XTRAC® excimer laser therapy to a new level. The campaign also drives awareness of the standard of care for psoriasis and vitiligo, attracting physicians outside of the dermatology discipline nationwide. As more physicians offer XTRAC®, PhotoMedex continues to close the gap between advancements and availability to improve patient care and lower healthcare costs.
We conducted a market survey in early January 2011 of both physicians and patients of our XTRAC therapy. The results indicated that physicians were aware of the technology and felt positively about it. However, patients were largely unaware of the XTRAC treatment. When patients were made aware of the treatment, they asked where they could find it. Based on the results of the survey, we believe that we can dramatically change the dynamics of this component of our business by increasing consumer awareness.

Seek to increase insurance reimbursement for vitiligo treatments using the XTRAC lasers. The XTRAC Excimer Laser is a procedure for psoriasis that is reimbursable by almost all major insurance companies, including Medicare. Although substantial improvement in the number of companies paying health insurance claims for vitiligo has recently occurred, it still lags behind psoriasis.


Professional Segment
Use PhotoMedex's 44-person U.S. direct sales force to increase sales of our professional products. Our current expertise in professional markets has opened channels for our LHE and Omnilux equipment. In addition, we intend to continue our international expansion and further the existing initiatives in Korea and India.
Our Products
We emphasize the development of physician-endorsed skin care products based on science. Once cleared for use by the required regulatory agencies, like the FDA, these products are commercialized through a systematic, proprietary marketing program that we view as integral to our business success. Some of our products, which are described in more detail below, are expected to be significant growth drivers for us. Our primary technology and product platforms are described below.
We evaluate four principal criteria in determining where to allocate product development resources:
demonstrable clinical efficacy and safety;
intellectual property protection;
cost of goods; and
market opportunity.
Specifically, new projects must be able to work effectively, but also have a low enough cost of goods to achieve a favorable price point for consumers and a favorable margin for us to advertise our products effectively. As well, the market should be well defined and large enough to accommodate the new product with room for growth as we ramp up marketing efforts.
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These platforms include the following:
Our Thermicon® technology and no!no!® product line;
Professional equipment built upon our Light and Heat Energy (LHE®) technology which is also incorporated into some of our consumer devices;
Our XTRAC® technology to treat psoriasis and vitiligo;
Our topical NEOVA® formulations to combat UV-induced damage causing premature skin aging;
Light-emitting diode (LED) technology used in our Omnilux™ and Lumière™ Light Therapy systems as well as in some of our consumer devices; and
Our Kyrobak® technology which incorporates Continuous Passive Motion (CPM) and Oscillation Therapy is for the relief of unspecified, lower back pain.
We also operate a surgical business, which includes the LaserPro® Diode surgical laser system and UniMax® family of laser micromanipulators for the delivery of laser energy in microsurgical procedures.
THERMICON® HEAT TRANSFER TECHNOLOGY
Our no!no!® hair removal products are built upon our proprietary heat-based Thermicon®brand technology to address consumer concerns over perceived limitations of existing hair removal products, including safety and pain, and to overcome inherent limitations of light-based hair removal solutions. Unlike other products that use methods that are painful, have side effects, are limited in body areas that can be treated or that emanate from the principle of selective thermolysis, the Thermicon® brand devices are based on heat only and are therefore applicable for all hair colors and skin types, can be used on all body areas, and if used per instructions do not have adverse events, and are virtually painless. Thermicon®brand devices utilize a high-temperature thermodynamic wire filament that is activated when the devices are moved in contact with and across the treatment area. We believe that the no!no!® brand hair removal products have several advantages over existing products for both the consumer and professional hair removal market, including:
Broad Applicability. Where other hair removal products such as shavers, waxing, threading and laser-based and intense pulsed light-based products are either limited by body area treated, are only effective at treating certain hair colors and skin types or are limited by the age of the consumer, products employing the Thermicon®brand devices technology, which do not rely upon light, are virtually painless and without side-effects and are equally effective across all hair colors and all skin types. Therefore, we believe that unlike other hair removal methods (such as shaving, threading and waxing), including light based devices, Thermicon®brand devices effectively remove hair on people with light hair or dark skin.
Compact Size. Since the Thermicon®brand devices do not require large energy sources or cooling systems, we are able to produce compact, hand-held, portable, reachable wireless products uniquely suitable for the consumer market, without sacrificing safety or efficacy.
Pain-Free. Many traditional hair-removal procedures, such as waxing or shaving, can cause nicks, cuts and significant pain. We believe that users of products employing the Thermicon®Brand devices experience only a mild tingling sensation.
Low Cost of Goods to MSRP ratio. Thermicon® brand technology has an average retail price of around $270 in the US and between $300-400 in other markets. In contrast, other hair removal methods, require consumers to undergo expensive in-office (or in-spa) visits for treatments that can cost several thousands of dollars. The Thermicon® brand platform enables a low cost of goods, and therefore a beneficial relationship cost of goods to MSRP.

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no!no!® Product Line: "Professional Technology Made for Consumers"
We have realized favorable market adoption of Thermicon® brand technology, which not only overcomes the challenges of other hair removal methods but also puts control of the hair removal process in consumers' hands.
We market a full line of consumer products based on the patented Thermicon® brand technology. These products are sold globally through infomercials and television shopping channels, retail stores, online shopping websites and worldwide strategic distribution agreements.
Since 2007, we have introduced a series of no!no! devices. Every product evolution—from the no!no! Classic™, the no!no! Hair™, the no!no! Hair for Men™, the no!no! Plus™ to the no!no! PRO 3™ and the no!no! PRO 5™—represents continued innovation and product line extension. Notably, each of the prior brands is still marketed even as we continue to introduce new product extensions like the no!no! Micro and no!no! Ultra launched in 2014. Going forward, we believe that the no!no! pipeline is considerable, with multiple new products and devices being developed with some that already have launched overseas. We are committed to effectively managing our product life cycle, seeking to ensure that, when there is a change in growth trajectory,time we will likely possess new, enhanced technologies that are synergistic with our platform.
no longer operate this business.

The no!no!® line of products also includes a consumables-based revenue model, which helps provide us with a growing, high-margin recurring revenue stream as consumers make repeat purchases of refill Thermicon tips, buffers and topical products.

LIGHT AND HEAT ENERGY (LHE®)
Our proprietary LHE® brand technology combines the benefits of direct heat and a full-spectrum light source. This technology is used primarily in our professional products, which entail capital equipment sold to physicians and skin care specialists worldwide. This technology has also been adapted to our hand-held consumer line of products like no!no! Skin, a medical devicesource for acne.
LHE capitalizes upon the principles of selective photothermolysis, which is a type of photo (or light-based) therapy in which heat is generated using selective absorption of light within the targeted tissue. Selective photothermolysis entails precisely targeting a pigmented tissue or structure with a specific wavelength of light that is absorbed into and limited to the target area but does not penetrate into the surrounding area. Heat is also produced and directed to the target with minimal effect on surrounding skin.
While there are many phototherapy options available for patients today, including laser and intense pulse light (IPL), we believe that we have optimized the light/heat relationship. Both Laser and IPL treatments filter out the heat given off by their flashes or pulses of light, primarily relying on the light energy to cause a clinical change. We believe that by not using the heat energy as well, laser and IPL technologies must be administered at high densities, which may require skin cooling techniques to protect patients from burns.
In contrast, LHE technology was developed with the objective of efficiently using both light and heat energy to provide a greater treatment advantage. In doing so, LHE® brand products can deliver less energy density (known as "low fluences") to the target skin area, which is believed to create a safer, more efficient product. We believe that lowering the fluence of our LHE® brand products reduces the need for skin cooling techniques, simplifies the treatment process and decreases the risk of harmful side effects. In addition, balancing light and heat enables phototherapy treatments for more sensitive skin types as well as a broader spectrum of hair colors.
We have incorporated patented internal filters that protect the skin during treatment with LHE technology. We also offer a specialized light unit assembly for use on sensitive skin to further enhance our products' safety and comfort without compromising results.
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As a result of our LHE technology, we have created an LHE® brand professional product line designed for clinical efficacy in a variety of clinical applications, including psoriasis care, acne treatment, skin tightening, skin rejuvenation, wrinkle reduction, collagen renewal, vascular and pigmented lesion treatments and hair removal. (Note that not all applications are clearedThis technology was originally used primarily in the U.S.)
We believe that LHE can be more attractive than both laserour professional products, including capital equipment sold to physicians and IPL technologies dueskin care specialists worldwide. The technology was then adapted to our cost structure, efficacy and easehand-held consumer line of application. Medical devices that use LHE can treat a larger spot size than a laser-based system, with less discomfort and without requiring post-treatment skin cooling. As well, our research finds that our LHE approach offers meaningful results for thin and/or light hair. The technology also enables the development of smaller equipment, which is more affordable than bulky laser systems for many clinicians.
Benefits of the LHE approach are summarized below.
Non-invasive, non-abrasive treatments;
No down time;
Clinically proven results;
Safety and efficacy for all skin types;
Especially suited for Skin Types V-VI; and
Easy to use
The no!no! Skin™
LHE® brand technology is also used in theproducts like no!no! Skin, a handheldmedical device for acne. Except for occasional sale of left over inventory, this business segment has basically ceased operations with the NEOVA sale September 23, 2016.

Sale of Prior Business

On March 31, 2016, we completed the sale to The Lotus Global Group, Inc. of all of the tangible and intangible assets of the Omnilux product line for $220 thousand ($110 thousand was received as a refundable deposit during December 2015 in advance and $110 thousand was received in April 2016), pursuant to the Agreement for Sale of Assets dated March 31, 2016. Management does not believe that the sale of the Omnilux product line represented a strategic shift for our company. As a result, the above transaction has not been reflected in the accompanying consolidated financial statements as discontinued operations (see Note 2, Discontinued Operations, to our consolidated financial statements). We recorded a loss on the disposal of those assets in the amount of $843 thousand for the year ended December 31, 2016.

On August 30, 2016, we entered into an Asset Purchase Agreement for the sale of our Neova product line. The sale was completed on September 15, 2016, resulting in immediate cash proceeds to us of $1.5 million and we recorded a loss of $1,731 thousand from the transaction during the third quarter ended September 30, 2016, and for the year ended December 31, 2016. The parties entered into several ancillary agreements as part of this transaction, including a Neova Escrow Agreement and a Neova Transition Services Agreement. Under the Neova Escrow Agreement, $250 thousand of the Purchase Price was placed into an escrow account held by U.S. Bank National Association as Escrow Agent. The funds were to remain in escrow until September 15, 2017, one year following the closing of the transaction. We received $158 thousand of these on December 13, 2017 and recognized an additional loss of $92 thousand on the sales of the Neova product line for the amount of funds withheld from the escrow account.

On October 4, 2016, we entered into an Asset Purchase Agreement with ICTV for the sale of our consumer division for $9.5 million, including $5 million in cash plus a $4.5 million royalty agreement. We also entered into a Transition Services Agreement, pursuant to which we agreed to provide ICTV with certain accounting, benefit, payroll, regulatory, IT support and other services for periods ranging from approximately three months to up to one year following the closing date, during which time ICTV would arrange to transition the services it receives to its own personnel.

This transaction was completed on January 23, 2017, (see Note 2 Discontinued Operations). We considered a number of factors before entering into the Asset Purchase Agreement, including, among other things, the price to be paid by ICTV, the strategic and financial benefits that the asset sale would provide to us, our extensive search process with respect to the sale of the business, the future business prospects of the business and the terms and conditions of the Asset Purchase Agreement. Ultimately, we concluded that the price offered by ICTV was a fair offer for the consumer products division.

On July 12, 2017, we entered into a Termination and Release Agreement under which the Asset Purchase Agreement described above was terminated and is of no further force and effect, except for certain surviving rights, obligations and covenants described in the Termination and Release Agreement. Pursuant to the Termination and Release Agreement, ICTV paid us $2 million in cash and we agreed that ICTV will have no further royalty or other payment obligations under the Asset Purchase Agreement. We derecognized the $4.5 million royalty receivable (which had been recognized on January 23, 2017) and recognized a total loss of $2 million in the nine-month period ended September 30, 2017, resulting in an adjustment of $2 million to the amount of the loss on the disposal of the asset. We had classified the assets of the consumer division as assets held for sale as of December 31, 2016.


As partial consideration for the releases provided by ICTV pursuant to the Termination and Release Agreement and in accordance with the terms therein, on July 12, 2017, we entered into a Bill of Sale and Assignment, which provides that we shall sell, assign, transfer, convey and deliver to ICTV, and ICTV purchase and accept from us, all of the right, title and interest, legal or equitable, in and to a deposit in the amount of $210 thousand held by a consumer division vendor, Sigmatron International, Inc., pursuant to an arrangement between us and Sigmatron International, Inc.

As part of the sale of the consumer product sold worldwide underline, which transaction was determined to represent a complete liquidation of a foreign subsidiary, the cumulative translation adjustment of $3,228 thousand related to that foreign entity was reclassified from accumulated other comprehensive income (loss) and reported as part of gain or loss from the sale.

Organizational Chart

The following chart depicts our no!no!® brand. The no!no! Skinorganizational structure following the sale of our prior business and the Contribution Transaction. All subsidiaries are wholly-owned unless otherwise indicated.

 

Our Real Estate Business

Our focus is to build our company into a 510(k)-cleared productleading real estate, asset management and development company, concentrating primarily on investments in high yield income producing assets and other opportunistic commercial properties via direct property ownership and asset management. Our objective is to generate long term net asset value growth while adhering to institutional best practices and a deep research process for all investments.


Income Producing Properties

For income producing properties, we intend to acquire assets that has been clinically demonstratedprovide recurring income with the potential for income growth over the long-term. We believe there can be an attractive risk/reward profile to resolve or improve acne lesions by 81% within 24 hours. It usessuch properties based on the same LHE® brand technology from our physician LHE® brand products but is optimized for home use.

The no!no! Skin puts out wide spectrum light (from 400 to 2,000 nm)location and gentle pulses of heat to penetrate blocked pores and stop acne at its source. The device seeks to pinpoint Propionibacterium acnes (P. acnes), or acne-causing bacteria, in the pore. The green light serves to stimulate the release of oxygen radicals, which attack the P. acnes. Simultaneously, the red light produces an anti-inflammatory reaction that reduces pimples' visible swelling. The addition of heat intensifies the process and gently opens the pores to release the clog and further soothe the inflammation.
The no!no! GLOW applies the same LHE® brand technology from our physician LHE® devices but is optimally miniaturized for home use.
KYROBAK
Kyrobak uses clinically proven, proprietary technology to treat unspecified, lower back pain. The unique combination of Continuous Passive Motion (CPM) and Oscillation therapy is a non-invasive, relaxing method for long lasting relief of back pain. Used for better than 3 decades in professional rehabilitation and chiropractic settings, CPM has been proven to increase mobilityunderlying credit attributes of the joints, draw more oxygentenants. In addition, we may invest in loans that are secured by income producing properties or ground leases on such properties. We believe that owning a diversified portfolio of actively managed properties and blood flowother real estate related investments can produce a consistent stream of income with long-term upside potential from income growth or redevelopment.

Real Estate Development

We look to invest in land assets that can be developed into income generating commercial, residential and hospitality properties, for-sale residential properties, or mixed-use development opportunities. Such properties may require extensive planning, and for these investments, we may partner with local developers, architects, and engineers to maximize the area, allowing the muscles to relaxhighest and release pressure between the vertebrae allowing the spine to open up and decompress.

Given that back pain is the leading cause of disability in Americans under the age of 45 and that it affects 25 Million Americans, from 25- 64, annually,best use. We focus on development properties where we believe the market needrisk profile is unfilled and the population underserved. Through our direct-to-consumer initiatives, we will be targeting the estimated 80% of Americans who have suffered lower back pain at least once in their lives with the Kyrobak brand device and a series of accessories poised to grow the brand further.
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XTRAC® EXCIMER LASERS
XTRAC is a legacy, ultraviolet (UV) light, excimer laser technology from Pre-merged PhotoMedex. It received an FDA clearance in 2000 and has since become a widely recognized treatment among dermatologists for psoriasis and other skin diseases for which there are no cures. Excimer lasers emit very concentrated UV light and are used in ophthalmology and dermatology practices. Our XTRAC brand lasers deliver ulta narrow-band ultraviolet B (UVB) light to affected areas of the skin in order to treat an array of skin conditions, including psoriasis and vitiligo, which combined affect up to 10.5 million people in the U.S. and 190 million people worldwide.
Present in natural sunlight, UVB is an accepted psoriasis treatment that penetrates the skin to slow the growth of damaged skin cells. UVB therapy occurs as patients expose their affected skin to a UVB light source for a set length of time on a regular schedule. In our XTRAC system, we have refined the delivery of optimum amounts of UVB directly to skin lesions. The XTRAC lasers emit a high-intensity beam of ultra-narrow-band UVB, which many studies prove can clear psoriasis faster and produce longer remissions than broad-band UVB. In comparison to broad-band UVB, narrow-band UVB also require fewer treatments to produce the desired effect.
We market two excimer laser brands: the XTRAC Ultra Plus and the XTRAC Velocity. The Velocity is a more advanced and faster machine, allowing clinicians to treat a greater surface area in a shorter period of time. It is designed to treat generalized psoriasis, but can be used for all disease levels (mild, moderate and severe).
The XTRAC products are sold to physicians primarily overseas, while in the US under a recurring revenue model, we generate incremental income on a per-use basis from these machines. We estimate that there are roughly 700 XTRAC lasers in use in the U.S., leaving considerablemisunderstood thus creating significant opportunity for growth, as the target U.S. audience for XTRAC lasers comprises approximately 3,500 dermatologists who perform disease management. This market excludes nearly 7,000 other U.S. dermatologists who are either in academia or not actively treating skin diseases.
To develop the XTRAC machines, our medical engineers and research team collaborated with Dr. Rox Anderson, director of the Wellman Center for Photomedicine at Massachusetts General Hospital, Harvard Medical School. The resulting device produced a monochromatic wavelength (308 nm) of UV light known to positively impact the psoriasis action spectrum.
We have found that XTRAC treatment leads to remission of patients' psoriasis in an average of 8 to 12 treatments. Treatment protocols recommend that patients receive two treatments per week with a minimum of 48 hours between treatments. Our data shows that XTRAC has an 89% efficacy and produces only minimal side effects. In support of its clinical effect, the XTRAC Excimer Lasers have been cited in over 45 clinical studies and research programs, with findings published in peer-reviewed medical journals around the world. The products have also been endorsed by the National Psoriasis Foundation, and their use for psoriasis is covered by nearly all major insurance companies, including Medicare.
XTRAC is a reimbursable procedure for psoriasis under three Current Procedural Terminology ("CPT") codes. It reimburses each treatment at approximately $175, with typical charges ranging from $150 to $250 depending on the amount of body surface being treated.
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Psoriasis Treatment Options
There are essentially three main types of psoriasis treatments, as listed below.
Topical therapies:
These can include corticosteroids, vitamin D3 derivatives, coal tar, anthralin and retinoids, among others, that are sold as a cream, gel, liquid, spray, or ointment. The efficacy of topical agents varies from person to person, although these products are commonly associated with a loss of potency over time as people develop resistance.
Phototherapy:
This is the area in which we operate. Our XTRAC Excimer Lasers are FDA-cleared, fully reimbursable, National Psoriasis Foundation-endorsed phototherapy treatments for psoriasis. In addition to treatment with XTRAC machines at a clinician's office, patients have the option of purchasing at-home UV light systems.
Systemic medications:There are a number of prescription medications available for psoriasis, which are given either by mouth or as an injection. Generally, these drugs are administered only after both topical treatments and phototherapy have failed, or for people who have severe disease or active psoriatic arthritis.
Ongoing Clinical Trial
The XTRAC® Excimer Lasers are particularly significant and beneficial for moderate and severe psoriasis patients who prefer a noninvasive treatment approach without the side effects of invasive, systemic agents, or to patients who have developed a resistance to topical agents. In many cases, UVB phototherapy can also be combined with topical or systemic medications in order to enhance efficacy. With this in mind, our XTRAC® lasers have been studied in a clinical trial in combination with Galderma Laboratories, L.P.'s topical psoriasis therapies Clobex and Vectical Ointment. Clobex is a topical corticosteroid cleared to treat moderate-to-severe plaque psoriasis. It is sold as a spray, shampoo, or lotion. Vectical Ointment is a topical treatment for mild-to-moderate plaque psoriasis. The trial was led by Dr. John Koo and Dr. Ethan Levin at the University of California, San Francisco.
The study's primary endpoint is to achieve a Psoriasis Area and Severity Index (PASI) score of 75 or better in 12 weeks and subsequently maintain that clearance for an extended period of time. A PASI 75 score indicates a 75% reduction in disease, and is a benchmark endpoint for most clinical trials of psoriasis. Preliminary results for the first 21 patients that completed the new XTRAC treatment protocol were reported in the Journal of Dermatological Treatment in February 19, 2014. By week 12, 76% of the patients had a reduction in Psoriasis Area and Severity Index of at least 75% (PASI-75) and 52% had a Physicians Global Assessment of "clear" or "almost clear." If this trend continues excimer laser therapy combined with an optimized topical agent may provide an extremely effective treatment of moderate and severe psoriasis that avoids the risk of serious side effects associated with many current systemic Biologic agents.
Using the XTRAC Excimer Lasers to Treat Vitiligo and Other Skin Diseases
UV light therapy is considered to be an effective and safe treatment for many skin disorders beyond psoriasis. To this effect, the XTRAC technology is FDA cleared for the treatment of not only psoriasis but also vitiligo (a skin pigment deficiency), atopic dermatitis (eczema) and leukoderma, which is a localized loss of skin pigmentation that occurs after an inflammatory skin condition, such as a burn, intralesional steroid injection, or post dermabrasion.
XTRAC technology works for vitiligo patients in much the same way as for psoriasis patients, although vitiligo treatment requires more therapy sessions. The XTRAC UVB light functions to reignite the skin's melanocytes (the cells that produce melanin), which causes pigment to return. To date, there is not sufficient data to confirm how long patients can expect their vitiligo to be in remission after XTRAC therapy. Based on anecdotal reports, we believe that re-pigmentation may last for several years.
Traditionally, vitiligo treatments have been considered cosmetic procedures, and as such, were not reimbursed by insurance companies. However, over the past two years, there has been a significant increase in insurance coverage for these procedures, although it still lags behind the widespread reimbursement for psoriasis.
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Due to a greater prevalence of vitiligo among people with darker skin types, regions such as the Middle East, where there is also a social stigma about the condition, are considerable markets for our XTRAC lasers.
Awareness of the positive effects of XTRAC treatments is the greatest limiting factor in making XTRAC treatments available to those who suffer from psoriasis and vitiligo. Therefore, we have initiated a direct to patient advertising campaign aimed at motivating psoriasis and vitiligo patients to seek out XTRAC treatments from our dermatologist customers. Specific advertisements encourage prospective patients to contact the Company's patient advocacy center through telephone or web site whereby we provide information on the treatment, insurance coverage and ultimately schedule an appointment for the prospective patient with one of our dermatologist customers for an evaluation and treatment regimen.
NEOVA® PHYSICIAN-DISPENSED SKIN CARE
Our NEOVA skin care line is designed as a therapeutic intervention for preventing premature skin aging due to UV-induced DNA damage. The topical technology seeks to repair photo-damaged skin using a novel combination of two key ingredients: DNA repair enzymes and our Copper Peptide Complex®. Copper has been studied for more than 20 years for its wound healing applications. Research suggests that copper can be used to improve the elasticity of skin and is complementary to DNA repair enzymes, which repair damage caused by sunlight and other UV rays.
The DNA repair enzymes contained in the NEOVA formulation have several objectives:
Continuously repair and enhance skin's natural processes;
Protect from UV immunosuppression;
Restore barrier function;
Promote collagen regeneration and skin elasticity; and
Assist in correcting and improving cell metabolism.
In concert with the repair enzymes, NEOVA's Copper Peptide Complex serves to promote new blood vessel growth and enhance the expression of growth factors. It stimulates collagen and elastin formation, which accelerate the repair process. Additionally, the Copper Peptide Complex is designed to mitigate damage caused by free radicals by promoting an antioxidant defense. Free radicals are a type of highly reactive oxygen molecule known to cause oxidative stress, which triggers harmful inflammatory responses and cell death as the free radicals attack DNA, lipids, proteins and other cell components. They are also believed to accelerate the progression of cancer, cardiovascular disease and age-related diseases, including cataracts, arthritis, Alzheimer's disease and diabetes. As typically occurs in normal, healthy cells, an antioxidant defense system comprising vitamins C and E and a variety of enzymes can minimize and repair free radical-induced damage.
Among other products, the NEOVA line includes DNA Damage Control SILC SHEER SPF 45, an award-winning tinted sunscreen that contains micronized titanium dioxide, organic blockers and DNA repair enzymes to reduce risks of skin cancer and premature aging—both of which are caused by photo damage from sun exposure. The DNA repair enzymes are clinically shown to reduce UV damage by 45% and increase UV protection by 300% in one hour.
NEOVA DNA Total Repair cream has been featured on The Doctors, a national daytime talk show that offers medical and health advice. The segment illustrated how the Total Repair product repairs damaged DNA in the cells of the skin in order to diminish age spots on someone who has used the cream consistently for two weeks. The guest testing the product reported that her hands had lightened considerably and some age spots had almost disappeared.
The NEOVA technology represents another opportunity to integrate our marketing platform with our direct sales force for plastic surgeons and dermatologists, which has traditionally been responsible for furthering market adoption of NEOVA products. Through a direct-to-consumer initiative, we seek to drive consumers to medical practices for NEOVA as well as to our website to buy direct.
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We hold over 13 patents related to the NEOVA technology, as well as the ability to draw upon more than 150 peer-reviewed journal articles that provide scientific support for these ingredients.
Our direct-to-consumer efforts are designed to take full selling advantage of the 10,000 attentive customers a week inquiring after no!no! products. Introduced as upsells to this population, the tests have shown significant success with 26% of customers opting-in for a Neova continuity program.
LED TECHNOLOGY
Omnilux™
Omnilux Light Therapy uses light-emitting diode (LED) technology to treat skin conditions. Although commonly understood for their use in electronics, LEDs have gained notoriety for medical applications as well. The Omnilux LED system is FDA cleared to treat wrinkles, acne, minor muscle pain and pigmented lesions. For professional use, the Omnilux equipment entails a common base apparatus equipped with three interchangeable headlamps. Each of these lamps gives off a different wavelength of light, which allows physicians to treat more than one condition with the same piece of capital equipment. Omnilux technology is believed to be applicable to all skin types. Going forward, we believe the application of LED technology will likely continue to expand, particularly as more research is conducted on the possibilities of using LEDs to activate cancer drugs, among other medications.
SURGICAL PRODUCTS
We engage in the development, manufacture and sale of surgical products, including proprietary free-beam and Contact Laser™ Systems for surgery. We introduced Contact Laser surgery by combining proprietary Contact Laser Delivery Systems with an Nd:YAG laser unit to create a multi-specialty surgical instrument that can cut, coagulate or vaporize tissue. Our Contact Laser Delivery Systems can be used effectively with any wavelength of laser between 532nm and 1064nm, including the KTP laser (532nm), diode laser (various wavelengths) and Nd:YAG laser (1064nm). We are currently marketing such products under the trade name PhotoMedex Surgical Products.
Our proprietary Contact Laser probe and scalpel surface treatments provide the ability to alter selectively the temperature profile of tissue, replicating the clinical effect of many different types of lasers. Through our Contact Laser Delivery Systems,if we are able to produceturn the development into a wide range of temperature gradients, which address a broad range of surgical procedures within multiple specialties. Our multiple-specialty capability reduces a hospital's need to purchase several lasers to meet its specialists' varied requirements.
Our LaserPro® Diode laser system has replaced the Nd:YAG laser as the preferred host laser for our Contact Laser Delivery Systems. Our Contact Laser Delivery Systems consist of proprietary fiberoptic delivery systems which deliver the laser beam from our Diode (or Nd:YAG) laser unit via an optical fiber to the tissue, either directly or through a proprietary Laser Probe or Laser Scalpel. These delivery systems can also be used with the laser systems of certain other manufacturers.
stabilized operating property.

Competition

The markets in which we participate are highly competitive. Certain of our competitors are larger than us and have substantially more resources. However, we believe that we are positioned to compete against a wide variety of peers, whether consumer-based companies of similar size or other companies competing in the aesthetics/physician channel. As it pertains to the aesthetic device market, this arena is complex and highly competitive—both for home use and treatment in a physician's office. Over the past several decades, the aesthetics technology market has changed considerably due to technological innovation and discoveries. We are exposed to competition from small, closely held, specialized aesthetic device companies, such as Dezac Group, Home Skinovations Ltd., TRIA Beauty, Inc. and LumaTherm Inc. Several public companies, such as Syneron Medical Ltd. (ELOS-NASDAQ), Cynosure Inc. (CYNO-NASDAQ) and Valeant Pharmaceuticals, Inc. (VRX-NYSE), are either looking to market or are already marketing consumer aesthetics products.
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Our no!no!® products are energy-based. As such, energy-based aesthetic products may face competition from non-energy-based medical products, such as shaving, tweezing, waxing and creams.

We believe that a significant barrier to entry into an applicable marketthe real estate business is the cost basis of the product, since our products are based upon a proprietary technology that allows us to build products inexpensively. From a marketing standpoint, if competitors are developing a product thatvery competitive. Our properties may compete with no!no!®, they then become tasked withlocal sites in attracting skilled labor during the challenge of building the marketing for that product.construction process and in attracting tenants and end-users upon completion. We invested roughly $62 million in 2014 in marketing and advertising. Furthermore, our comprehensive intellectual property position may serve as a deterrent to companies.

We may also compete with pharmaceutical compoundsseveral types of real estate investors for acquisitions of properties, including real estate limited partnerships and methodologies used to treat an arrayprivate equity, REITs, developers, financial institutions, and individuals that own, manage, finance or develop properties. Many of skin conditions addressed by our professional products. Such alternative treatments may be in the form of topical products, systemic medications,these groups have larger operations and phototherapies from both large pharmaceutical and smaller laser companies. Currently, our XTRAC system is believed to be a competitive therapy to alternative treatments on the basis of its recognized clinical effect, cost-effectiveness and reimbursement. Potential competition for us in this category could come from Biogen Idec Inc. (BIIB-NASDAQ), Centocor, Inc. (a Johnson & Johnson company) and Abbott Laboratories (ABT-NYSE), which are engaged in R&D and commercialization of treatments in these areas. In some cases, these companies have already received FDA approval for products or commenced clinical trials for such treatments.
With regard to surgical lasers,greater financial resources than we face substantial competition from other manufacturers of surgical laser systems, whose identity varies depending on the medical application for which the surgical system is being used and from traditional surgical methods. Other companies are developing competitive surgical systems and related technologies.
We currently face competitors offering discounted prices in some geographic markets where we conduct business. It is possible that our business could be materially adversely affected in the future by discounting practices of competitors, including from both a price and volume perspective. Laser vision correction procedure volume has historically correlated with the Consumer Confidence Index. In individual markets, our challenge is to leverage the national strengths of our company and enhance local efforts in order to grow market share.
Manufacturing
We manufacture our excimer laser products and our excimer lamp product at our 11,300 sq. ft. facility in Carlsbad, California. Our California facility is ISO 13485 certified. ISO 13485 is an International standardization written by the International Organization for Standardization, which publishes requirements for a comprehensive quality management system for the design and manufacture of medical devices. Certification to the standard is awarded by accredited third parties. do.

We believe that our present manufacturing capacity at these facilities is sufficientsize and scale provide an opportunity to meet foreseeable demand for our products.

For our surgical products, we manufacturetake advantage of smaller-tier assets that most of our own componentstraditional investors do not focus on due to size limitations, thus creating unique investment opportunities with attractive risk/reward profiles.

Investment Strategy

Our diversified investment strategy provides us with flexibility to invest across real estate asset classes and utilize certain suppliers for the manufacture of selected standard components and subassemblies, which are manufactured to our specifications. Most major components and raw materials, including optics and electro-optic devices, are available from a variety of sources. We conduct all final testing and inspection of our products. We have established a quality control program, including a set of standard manufacturing and documentation procedures intended to ensure that, where required, our products are manufactured in accordance with applicable FDA regulations and the comparable requirements of the European Community and other countries, including for example Japan and Canada.

Outsourcing and Fulfillment
We out-source the manufacturing of our Thermicon® and LHE® brand products while maintaining control over the production process. We believe that by outsourcing the manufacturing of each product, we can maintain low inventory levels and fixed unit costs, with minimal infrastructure, without incurring significant capital expenditures. We use third-party contract manufacturers and suppliers to obtain substantially all of the related product and packaging components and to manufacture these finished products. We believe that we have good

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relationships with our manufacturers and suppliers and that there are alternative sources in the event that one or more of these manufacturers or suppliers is not available or cease the conduct of its business. We continually review our manufacturing and supply needs against the capacity of our contract manufacturers and suppliers with the objective of ensuring that we are able to meet our production goals, reduce costs and operate more efficiently.
We contract with third-party fulfillment vendors to package and distribute our Thermicon®, LHE® and skincare products primarily from our fulfillment facilitiessubmarkets in the United States Canada and globally. We will look to utilize our industry experience and relationships to identify the United Kingdom.
transactions which generate the most attractive risk / reward opportunities consistent with our strategy. We substantially outsource the manufacturingenforce a rigorous and repeatable underwriting process based on deep research and due diligence.

One of our Skin Care productscore strategies is that we intend to OEM contract manufacturers. In addition, we currently out-sourcefind investments in secondary and tertiary markets with assets that require minimal capital expenditures but generate initial unlevered cash flow yields that are higher than those in primary markets. We look to acquire assets in submarkets where the manufacturingpopulation and employment trends are positive and where the underlying asset serves a key purpose to the local community.

A second component of our LED products. The LED product equipmentinvestment strategy will revolve around sourcing asset management opportunities for which we would operate as an asset manager of real estate properties. We are not currently structured as a REIT, thus we have the ability to retain earnings and to operate in real estate asset management, development and peripheral real estate activities, items that may be limited by REIT requirements. We will look to utilize our existing infrastructure to provide efficiencies of scale to owners of real estate assets as we grow our portfolio over time.

Our criteria for evaluating investments includes, but is currently manufactured by an OEM manufacturer innot limited to, submarket location of the UK with tooling providedasset, economic and owned by us. We believe thatpopulation growth fundamentals of the manufacturing capacitylocation, credit quality of this supplier is sufficiently adequate for anticipated demand. Quality control is performedthe tenant, terms of the underlying leases, historical cash flow and capital expenditure needs at the OEM manufacturerproperty, ability to acquire financing secured by the property, tax and atregulatory risks associated with the investment, environmental and structural attributes of the property, long-term viability of the asset, and potential redevelopment opportunities of the real estate.

We do extensive research on these investment attributes when preparing our facilitiesinvestment memorandum. We compare the real estate acquisition we are making to other investments with similar risk profiles both inside and outside the direct real estate investment sector to best assess the merits of the opportunity.


Existing Portfolio

In 2017, we acquired (i) three vacant land sites intended for development as gas stations in the U.S. The hand-held devicesnorthern California, (ii) a majority membership interest in a limited liability company that owns a vacant land site located in Northern California, and the consumable products are manufactured by(iii) an OEM manufacturerinterest in Carlsbad, CA. We are currently reliant ona limited liability company which owns property located in Los Lunas, New Mexico being developed as a single supplier for LEDs.family residential development.

Our Intellectual Property

We do not have any material intellectual property rights relating to our real estate business. However, we do employ certain proprietary processes related to the real estate business which are protected as trade secrets of our company. We have not, hadat this time, registered any difficulties in product supply of LEDspatents, trademarks or copyrights associated with our real estate business and do not expect to date, but we are actively seeking an alternate supplier for the purpose of offsetting this single-supplier approach.

Researchdo so.

Our legacy global skin health business provided integrated disease management and Development

As of March 13, 2015, our researchaesthetic solutions to dermatologists, professional aestheticians and development team, including engineers, consisted of 13 employees.consumers. We conduct research and development activities at three of our facilities located in Horsham, Pennsylvania, Carlsbad, California and Hod Hasharon, Israel. Our research and development expenditures were approximately $3.1 million in 2014, $3.3 million in 2013 and $2.9 million in 2012.
Our research and development activities are focused on:
the utilization of existing technologies to develop additional consumer and professional applications and products;
the application of our XTRAC system to the treatment of inflammatory skin disorders;
the development of complementary devices to further improve the phototherapy treatments performed with our XTRAC and other light-based systems;
the development of new skin health and hair care products; and
the development of additional products and applications, whether in phototherapy or surgery, by working closely with our Scientific Advisory Board, medical centers, universities and other companies worldwide.
Patents and Proprietary Technologies
We intend to protectprotected our proprietary rights relating tour legacy business from unauthorized use by third parties to the extent that our proprietary rights arewere covered by valid and enforceable patents, trademarks, trade names or arecopyrights, or were effectively maintained as trade secrets.
Our

Historically, our policy iswas to file patent applications and to protect certain technology, inventions and improvements that are commercially important to the development of our business. As patents expire and expose our inventions to public use, we seeksought to mitigate the impact of such expirations by seeking protection of improvements. The patents in our Skin Care product line relate to use of our copper and manganese peptide-based technology for a variety of healthcare applications and to the composition of certain biologically active, synthesized compounds. Our strategy has been to apply for and maintain patent protection for certain compounds and their discovered uses that are believed to have potential commercial value in countries that offer significant market potential. As of December 31, 2014, we had 127 issued patents and 61 patent applications. In the U.S. alone, our business is protected by 34 patents.

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We have licensed certain of our proprietary technology to third parties. We seek licenses from third parties for technology that can broaden our product and service offerings. For example, we secured a license from the Mount Sinai School of Medicine, New York, New York, which granted us exclusive rights to a patent directed to the use of excimer lasers in the treatment of vitiligo.
We also relyrelied on trade secrets, employee and third-party nondisclosure agreements and other protective measures to protect our intellectual property rights pertaining to our products and technology.
Many of our

Our products and services arewere offered under trademarks and service marks, both registered and unregistered. We believe our trademarks encourageencouraged customer loyalty and aidaided in the differentiation of our products from competitors'competitors’ products. In connection with the sales of our Neova product line and our consumer products especially in our skincare products.division, we transferred the intellectual property associated with those product lines, including trademarks and trade names, to their respective purchasers. Accordingly, we had 25320 trademarks, either registered or being registered, in markets around the world that we intend to maintain in support of our real estate business and our legacy capital equipment products. These include 449 trademarks issued in the U.S. and 17511 trademarks issued in the rest of the world. We periodically reviewreviewed the trademarks in our portfolio for usefulness with our then existing and anticipated product lines; as a result, certain trademarks which were no longer in use in our business were not renewed.

Research and Development

Our research and development expenditures relating to our legacy business operations were approximately $143 thousand in 2017 and $1.2 million in 2016. As of January 23, 2017, the research and development personnel were transferred to ICTV in connection with the closing of the sale of the consumer product line assets.

Government Regulation

Regulations Relating to Legacy Business

Regulations Relating to Products and Manufacturing

Our products and research and development activities are regulated by numerous governmental authorities, principally the U.S. Food and Drug Administration or the FDA and corresponding state and foreign regulatory agencies. Any medical device or cosmetic we manufacture and/or distribute willwould be subject to pervasive and continuing regulation by the FDA. The U.S. Food, Drug and Cosmetics Act, or FD&C Act, and other federal and state laws and regulations govern the pre-clinical and clinical testing, design, manufacture, use, labeling and promotion of medical devices, including our XTRAC system, LED devices, surgical lasers and other products currently under development by us and govern the manufacture and labeling of the cosmetic products. Product development and approval for medical devices within this regulatory framework takes a number of years and involves the expenditure of substantial resources.

In the U.S., medical devices are classified into three different classes, Class I, II and III, on the basis of controls deemed necessary to provide a reasonable assurance of the safety and effectiveness of the device. Class I devices are subject to general controls, such as facility registration, medical device listing, labeling requirements, premarket notification (unless the medical device has been specifically exempted from this requirement), adherence to the FDA's Quality System Regulation, and requirements concerning the submission of device-related adverse event reports to the FDA. Class II devices are subject to general and special controls, such as performance standards, pre-market notification (510(k) clearance), post-market surveillance, and FDA Quality System Regulations. Generally, Class III devices are those that must receive premarket approval by the FDA to provide a reasonable assurance of their safety and effectiveness, such as life-sustaining, life-supporting and implantable devices, or new devices that have been found not to be substantially equivalent to existing legally marketed devices.
With limited exceptions, before a new medical device can be distributed in the U.S., marketing authorization typically must be obtained from the FDA through a premarket notification under Section 510(k) of the FDA Act, or through a premarket approval application under Section 515 of the FDA Act. The FDA will typically grant a 510(k) clearance if it can be established that the device is substantially equivalent to a predicate device that is a legally marketed Class I or II device (or to pre-amendments Class III devices for which the FDA has yet to call for premarket approvals). We have received FDA 510(k) clearance to market our XTRAC system for the treatment of psoriasis, vitiligo, atopic dermatitis and leukoderma and to market our LED products for a variety of indications for use. Additionally, the FDA has issued clearances to commercially market our Contact Laser System (which includes the system's laser unit, laser probes, laser scalpels and fiberoptic delivery systems) in a variety of surgical specialties and procedures in gynecology, gastroenterology, urology, pulmonology, general and plastic surgery, cardiothoracic surgery, ENT surgery, ophthalmology, neurosurgery and head and neck surgery. The FDA granted these clearances under Section 510(k) on the basis of substantial equivalence to other laser or electrosurgical cutting devices that had received prior clearances.
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For any devices that are cleared through the 510(k) process, modifications or enhancements that could significantly affect the safety or effectiveness of the device, or that constitute a major change in the intended use of the device, will require a new 510(k) submission. In August 2003, the FDA granted 510(k) clearance for a significantly modified version of our XTRAC laser, which we have marketed as the XTRAC XL Plus™ Excimer Laser System. In October 2004, the FDA granted clearance for the XTRAC Ultra™ (AL 8000) Excimer Laser System and, in March 2008, we received 510(k) clearance for the XTRAC Velocity™ (AL 10000) Excimer Laser System.
To date, we have not been required to secure premarket approval for our devices. A premarket approval application may be required for a Class II device if it is not substantially equivalent to an existing legally marketed Class I or II device (or a pre-amendments Class III device for which the FDA has yet to call for premarket approval) or if the device is a Class III premarket approval device by regulation. A premarket approval application must be supported by valid scientific evidence to demonstrate a reasonable assurance of safety and effectiveness of the device, typically including the results of clinical trials, bench tests and possibly animal studies. In addition, the submission must include, among other things, the proposed labeling. The premarket approval process can be expensive, uncertain and lengthy and a number of devices for which FDA approval has been sought by other companies have never been approved for marketing.
We are subject to routine inspection by the FDA and, as noted above, must comply with a number of regulatory requirements applicable to firms that manufacture medical devices and other FDA-regulated products for distribution within the U.S., including requirements related to device labeling (including prohibitions against promoting products for unapproved or off-label uses), facility registration, medical device listing, labeling requirements, adherence to the FDA's Quality System Regulation, good manufacturing processes and requirements for the submission of reports regarding certain device-related adverse events to the FDA.
We are also subject to the radiological health provisions of the FDA Act and the general and laser-specific radiation safety regulations administered by the Center for Devices and Radiological Health, or CDRH, of the FDA. These regulations require laser manufacturers to file initial, new product, supplemental and annual reports, to maintain quality control, product testing and sales records, to incorporate certain design and operating features (depending on the class of product) in lasers sold to end users pursuant to a performance standard and to certify and appropriately label each laser sold as belonging to one of four classes, based on the level of radiation from the laser that is accessible to users. Moreover, we are obligated to repair, replace, or refund the cost of certain electronic products that are found to fail to comply with applicable federal standards or otherwise are found to be defective. The CDRH is empowered to seek fines and other remedies for violations of the regulatory requirements. To date, we have filed the documentation with the CDRH for our laser products requiring such filing and have not experienced any difficulties or incurred significant costs in complying with such regulations.

We have received approval from the European Union to affix the CE Mark to our XTRAC laser system, VTRAC™ lamp system, Omnilux LED system and our diode laser system.LHE products. This certification is a mandatory conformity mark for products placed on the market in the European Economic Area, which is evidence that they meet all European Community, or EC, quality assurance standards and compliance with applicable European medical device directives for the production of medical devices. This will enable us to market our approved products in all of the member countries that accept the CE Mark. We also will be required to comply with additional individual national requirements that are in addition to those required by these nations. Our products have also met the requirements for marketing in various other countries.


Failure to comply with applicable regulatory requirements can result in fines, injunctions, civil penalties, recalls or seizures of products, total or partial suspensions of production, refusals by the U.S and foreign governments to permit product sales and criminal prosecution.

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As to our cosmetic products, the FD&C Actprosecution and the regulations promulgated there and under other federal and state statutes govern the testing, manufacture, safety, labeling, storage, record-keeping, advertising and promotion of cosmetic products. Our cosmetic products and product candidates may be regulated by any of the various FDA Centers. Routinely, however, cosmetics are regulated by the FDA's Center for Food Safety and Applied Nutrition. In other countries, cosmetic products may also be regulated by similar health and regulatory authorities. The skin care business also has two devices (e.g. wound care dressings) subject to 510(k) clearance, four products (e.g. sunscreen products) that contain drugs approved for use in over-the-counter products, and one prescription drug. Currently, the skincare products that are classified as drugs are not required to obtain pre-marketing regulatory approval. The process of obtaining and maintaining regulatory approvals in the U.S. and abroad for the manufacturing or marketing of our existing and potential skincare products is potentially costly and time-consuming and is subject to unanticipated delays. Regulatory requirements ultimately imposed could also adversely affect our ability to clinically test, manufacture or market products.
Failure to obtain regulatory approvals where appropriate for our cosmetic, device or drug product candidates or to attain or maintain compliance with quality system regulations or other manufacturing requirements, could have a material adverse effect on our business, financial condition and results of operations.
We are or may become subject to various other federal, state, local and foreign laws, regulations and policies relating to, among other things, safe working conditions, good laboratory practices and the use and disposal of hazardous or potentially hazardous substances used in connection with research and development.

Fraud and Abuse Laws

Because of the significant federal funding involved in Medicare and Medicaid, Congress and the states have enacted, and actively enforce, a number of laws whose purpose is to eliminate fraud and abuse in federal health care programs. Our business is subject to compliance with these laws.

Anti-Kickback Laws

In the U.S., there are federal and state anti-kickback laws that generally prohibit the payment or receipt of kickbacks, bribes or other remuneration in exchange for the referral of patients or other health-related business. The U.S. federal healthcare programs'programs’ Anti-Kickback Statute makes it unlawful for individuals or entities knowingly and willfully to solicit, offer, receive or pay any kickback, bribe or other remuneration, directly or indirectly, in exchange for or to induce the purchase, lease or order, or arranging for or recommending purchasing, leasing, or ordering, any good, facility, service, or item for which payment may be made in whole or in part under a federal healthcare program such as Medicare or Medicaid. The Anti-Kickback Statute covers "any“any remuneration," which has been broadly interpreted to include anything of value, including for example gifts, certain discounts, the furnishing of free supplies, equipment or services, credit arrangements, payments of cash and waivers of payments. Several courts have interpreted the statute'sstatute’s intent requirement to mean that if any one purpose of an arrangement involving remuneration is to induce referrals of federal healthcare covered business, the arrangement can be found to violate the statute. Penalties for violations include criminal penalties and civil sanctions such as fines, imprisonment and possible exclusion from Medicare, Medicaid and other federal healthcare programs. In addition, several courts have permitted kickback cases brought under the Federal False Claims Act to proceed, as discussed in more detail below.

Because the Anti-Kickback Statute is broadly written and encompasses many harmless or efficient arrangements, Congress authorized the Office of Inspector General of the U.S. Department of Health and Human Services, or OIG, to issue a series of regulations, known as "safe“safe harbors." For example, there are regulatory safe harbors for payments to bona fide employees, properly reported discounts and rebates, and for certain investment interests. Although an arrangement that fits into one or more of these exceptions or safe harbors is immune from prosecution, arrangements that do not fit squarely within an exception or safe harbor do not necessarily violate the statute. The failure of a transaction or arrangement to fit precisely within one or more of the exceptions or safe harbors does not necessarily mean that it is illegal or that prosecution will be pursued. However, conduct and business arrangements that arguably implicate the Anti-Kickback Statute but do not fully satisfy all the elements of an exception or safe harbor may be subject to increased scrutiny by government enforcement authorities such as the OIG.

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Many states have laws that implicate anti-kickback restrictions similar to the Anti-Kickback Statute. Some of these state prohibitions apply, regardless of whether federal health care program business is involved, to arrangements such as for self-pay or private-pay patients.

Government officials have focused their enforcement efforts on marketing of healthcare services and products, among other activities, and recently have brought cases against companies, and certain sales, marketing and executive personnel, for allegedly offering unlawful inducements to potential or existing customers in an attempt to procure their business.

Federal Civil False Claims Act and State False Claims Laws

The federal civil False Claims Act imposes liability on any person or entity who, among other things, knowingly and willfully presents, or causes to be presented, a false or fraudulent claim for payment by a federal healthcare program, including Medicare and Medicaid. The "qui“qui tam," or "whistleblower"“whistleblower” provisions of the False Claims Act allow a private individual to bring actions on behalf of the federal government alleging that the defendant has submitted a false claim to the federal government, and to share in any monetary recovery. In recent years, the number of suits brought against healthcare providers by private individuals has increased dramatically. Medical device companies, like us, can be held liable under false claims laws, even if they do not submit claims to the government, when they are deemed to have caused submission of false claims by, among other things, providing incorrect coding or billing advice about their products to customers that file claims, or by engaging in kickback arrangements with customers that file claims.


The False Claims Act also has been used to assert liability on the basis of misrepresentations with respect to the services rendered and in connection with alleged off-label promotion of products. Our future activities relating to the manner in which we sell our products and document our prices, such as the reporting of discount and rebate information and other information affecting federal, state and third-party reimbursement of our products, and the sale and marketing of our products, may be subject to scrutiny under these laws.

When an entity is determined to have violated the False Claims Act, it may be required to pay up to three times the actual damages sustained by the government, plus civil penalties of $5,500five to $11,000eleven thousand dollars for each separate false claim. There are many potential bases for liability under the False Claims Act. A number of states have enacted false claim laws analogous to the federal civil False Claims Act and many of these state laws apply where a claim is submitted to any state or private third-party payor. In this environment, our engagement of physician consultants in product development and product training and education could subject us to similar scrutiny. We are unable to predict whether we would be subject to actions under the False Claims Act or a similar state law, or the impact of such actions. However, the costs of defending such claims, as well as any sanctions imposed, could significantly affect our financial performance.

HIPAA Fraud

Regulations Relating Real Estate Business

Federal, State and/or Local Regulatory Compliance

We are, or will be, subject to a variety of Federal, state and/or local statutes, ordinances, rules, and Other Regulations

The Health Insurance Portabilityregulations covering the purchase, development, construction and Accountability Actoperation of 1996,real estate assets. These regulatory requirements include zoning and land use, building design, construction, worksite safety, traffic, and other matters, such as local rules that may impose restrictive zoning and developmental requirements. We are, or HIPAA, created a class of federal crimes known as the "federal health care offenses," including healthcare fraudwill be, subject to various licensing, registration, and false statements relating to healthcare matters. The HIPAA health care fraud statute prohibits, among other things, knowingly and willfully executing, or attempting to execute, a scheme or artifice to defraud any healthcare benefit program, or to obtain by means of false of fraudulent pretenses, any money under the control of any health care benefit program, including private payors. A violation of this statute is a felony and may result in fines, imprisonment and/or exclusion from government-sponsored programs. The HIPAA false statements statute prohibits, among other things, knowingly and willfully falsifying, concealing or covering up a material fact or making any materially false, fictitious or fraudulent statement or representationfiling requirements in connection with the deliverydevelopment, construction, advertisement, and sale of or payment for healthcare benefits, items or services. A violation of this statute is a felony and may result in finescertain real estate assets. Additionally, state and/or imprisonment. Entities that are found to have aided or abettedlocal governmental agencies may impose moratoriums on new construction in a violation of the HIPAA federal health care offenses are deemed by statute to have committed the offense and are punishable as a principal.
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We are also subjectan area due to the U.S. Foreign Corrupt Practices Actneed for infrastructure development, including road development and similar anti-bribery laws applicable in non-U.S. jurisdictions that generally prohibit companies and their intermediaries from making improper paymentsutility remediation. Finally, state and/or local governments retain certain rights with respect to non-U.S. government officials for the purpose of obtainingeminent domain which could enable them to restrict or retaining business. Because of the predominance of government-sponsored healthcare systems around the world, most of our customer relationships outside of the U.S. will be with governmental entities and therefore subject to such anti-bribery laws.
HIPAA and Other Privacy Regulations
The regulations that implement HIPAA also establish uniform standards governing the conduct of certain electronic healthcare transactions and protecting the security and privacy of individually identifiable health information maintained or transmitted by healthcare providers, health plans and healthcare clearinghouses, which are referred to as "covered entities." Several regulations have been promulgated under HIPAA's regulations including: the Standards for Privacy of Individually Identifiable Health Information, or the Privacy Rule, which restricts the use and disclosure of certain individually identifiable health information; the Standards for Electronic Transactions, or the Transactions Rule, which establishes standards for common healthcare transactions, such as claims information, plan eligibility, payment information and the use of electronic signatures; and the Security Standards for the Protection of Electronic Protected Health Information, or the Security Rule, which requires covered entities to implement and maintain certain security measures to safeguard certain electronic health information. Although we do not believe we are a covered entity and therefore are not currently directly subject to these standards, we expect that our customers generally will be covered entities and may ask us to contractually comply with certain aspects of these standards by entering into requisite business associate agreements. While the government intended this legislation to reduce administrative expenses and burdens for the healthcare industry, our compliance with certain provisions of these standards entails significant costs for us.
The Health Information Technology for Economic and Clinical Health Act, or the HITECH Act, which was enacted in February 2009, strengthens and expands the HIPAA Privacy and Security Rules and the restrictions on use and disclosure of patient identifiable health information. HITECH also fundamentally changed a business associate's obligations by imposing a number of Privacy Rule requirements and a majority of Security Rule provisions directly on business associates that were previously only directly applicable to covered entities. HITECH includes, but is not limited to, prohibitions on exchanging patient identifiable health information for remuneration, restrictions on marketing to individuals, and obligations to agree to provide individuals an accounting of virtually all disclosures of their health information. Moreover, HITECH requires covered entities to report any unauthorized use or disclosure of patient identifiable health information, known as a breach, to the affected individuals, the United States Department of Health and Human Services, or HHS, and, depending on the size of any such breach, the media for the affected market. Business associates are similarly required to notify covered entities of a breach. Most of the HITECH provisions became effective in February 2010. HHS has already issued regulations governing breach notification which were effective in September 2009.
HITECH has increased civil penalty amounts for violations of HIPAA by either covered entities or business associates up to an annual maximum of $1.5 million for uncorrected violations based on willful neglect. Imposition of these penalties is more likely now because HITECH significantly strengthens enforcement. It requires HHS to conduct periodic audits to confirm compliance beginning in February 2010 and to investigate any violation that involves willful neglect which carries mandatory penalties beginning in February 2011. Additionally, state attorneys general are authorized to bring civil actions seeking either injunctions or damages in response to violations of HIPAA Privacy and Security Rules that threaten the privacy of state residents.
In addition to federal regulations issued under HIPAA, some states have enacted privacy and security statutes or regulations that, in some cases, are more stringent than those issued under HIPAA. In those cases, it may be necessary to modify our planned operations and procedures to comply with the more stringent state laws. If we fail to comply with applicable state laws and regulations, we could be subject to additional sanctions.
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Federal and state consumer protection laws are being applied increasingly by the United States Federal Trade Commission, or FTC, and state attorneys general to regulate the collection, use, storage and disclosure of personal or patient information, through websites or otherwise, and to regulate the presentation of web site content. Courts may also adopt the standards for fair information practices promulgated by the FTC, which concern consumer notice, choice, security and access. Numerous other countries have or are developing laws governing the collection, use, disclosure and transmission of personal or patient information.
HIPAA as well as other federal and state laws apply to our receipt of patient identifiable health information in connection with research and clinical trials. We collaborate with other individuals and entities in conducting research and all involved parties must comply with applicable laws. Therefore, the compliance of the physicians, hospitals or other providers or entities with whom we collaborate also impacts our business.
Third-Party Reimbursement
Our ability to market our phototherapy products successfully depends in large part on the extent to which various third parties are willing to reimburse patients or providers for the cost of medical procedures utilizing our treatment products. These third parties include government authorities, private health insurers and other organizations, such as health maintenance organizations. Third-party payors are systematically challenging the prices charged for medical products and services. They may deny reimbursement if they determine that a prescribed device is not used in accordance with cost-effective treatment methods as determined by the payor, or is experimental, unnecessary or inappropriate. Accordingly, if less costly drugs or other treatments are available, third-party payors may not authorize, or may limit, reimbursement foralter the use of our products,property. These requirements may lead to increases in the Company’s overall costs. The need to comply with these requirements may significantly delay development and/or construction with regard to properties, or lead us to alter our plans regarding certain real estate assets. Some requirements, on a property by property evaluation, may lead to a determination that development of a particular property would not be economically feasible, even if any or all necessary governmental approvals were obtained.

Environmental Regulatory Compliance

Under various Federal, state and/or local laws, ordinances and regulations, a current or previous owner or operator of a property may be required to investigate and/or clean-up hazardous or toxic substances released at that property. That owner or operator also may be held liable to third parties for bodily injury or property damage (investigation and/or clean-up costs) incurred by those parties in connection with the contamination at that site. These laws often impose liability without regard to whether the owner or operator knew of or otherwise caused the release of the hazardous or toxic substances. In addition, persons who arrange for the disposal or treatment of hazardous substances or other regulated materials also may be liable for the costs of removal or remediation of such substances at a disposal or treatment facility, whether or not such facility is owned or operated by such persons.

The costs of remediation or removal of hazardous or toxic substances can be substantial, and the presence of contamination, or the failure to remediate contamination discovered, at a property we own or operate may adversely affect our products are saferability to develop, construct on, sell, lease, or more effective thanborrow upon that property. Current and former tenants at a property we own may have, or may have involved, the alternatives. Additionally, theyuse of hazardous materials or generated hazardous wastes, and those situations could result in our incurring liabilities to remediate any resulting contamination if the responsible party is unable or unwilling to do so.

In addition, our properties may require changesbe exposed to a risk of contamination originating from other sources. While a property owner generally is not responsible for remediating contamination that has migrated on-site from an off-site source, the contaminant’s presence could have adverse effects on our pricing structure and revenue model before authorizing reimbursement.

Reimbursement systems in international markets vary significantly by country and by region within some countries, and reimbursement approvals must be obtainedability to develop, construct on, operate, sell, lease, or borrow upon that property. Certain environmental laws may create a lien on a country-by-country basis. Many international marketscontaminated site in favor of the government for damages and costs the government may incur to remediate that contamination. Moreover, if contamination is discovered on a property, environmental laws may impose restrictions on the manner in which that property may be used, or how businesses may be operated on that property, thus reducing our ability to maximize our investment in that property. Our properties have government-managed healthcare systems that control reimbursement forbeen subjected to varying degrees of environmental assessment at various times; however, the identification of new devicesareas of contamination, a change in the extent or known scope of contamination, or changes in environmental regulatory standards and/or cleanup requirements could result in significant costs to us.


Employees

As of March 31, 2018, we had 4 full-time employees devoted to the ongoing business of our company, which consisted of 2 executive officers and procedures. In most markets, there are private insurance systems,2 finance, legal and administration staff, as well as government-managed systems. Our XTRAC products remain substantially without approval for reimbursement in many international markets under either government or private reimbursement systems. Since our skincare products are primarily for cosmetic applications, reimbursement is not a critical factor in growing revenues for this product segment.

Many private plans key their reimbursement rates to rates set by the Centers for Medicare and Medicaid Services (CMS) under three distinct Current Procedural Terminology (CPT) codes based on the total skin surface area being treated
..
As of December 31, 2014, the national rates were as follows:
96920 – designated for: the total area less than 250 square centimeters. CMS assigned a 2015 national payment of approximately $156.25 per treatment;
96921 – designated for: the total area 250 to 500 square centimeters. CMS assigned a 2015 national payment of approximately $172.70 per treatment; and
96922 – designated for: the total area over 500 square centimeters. CMS assigned a 2015 national payment of approximately $238.84 per treatment.
The national rates are adjusted by overhead factors applicable to each state.
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Employees
As of March 13, 2015, we had 179 full-time employees, which consisted of two executive officers, 17 senior managers, 83 sales and marketing staff, 30 people engaged in operations, 12 customer-field service personnel, 13 engaged in research and development, including 7 engineers, and 22 finance and administration staff. We intend to hire additional sales personnel as the development of our business makes such action appropriate. The loss of the services of key employees could have a material adverse effect on our business. Since there is intense competition for qualified personnel knowledgeable in our industry, no assurances can be given that we will be successful in retaining and recruiting needed personnel2 part-time employees..

Our employees are not represented by a labor union nor covered by a collective bargaining agreement. We believe that we have good relations with our employees.

Financial Information about Geographic Areas
See Note 15 to the consolidated financial statements included elsewhere in this filing.

Available Information

PhotoMedex's

Our website is www.photomedex.com.www.fcglobalrealty.com. Our annual reports on Form 10-K, quarterly reports on 10-Q, current reports on Form 8-K, and amendments to those reports filed or furnished pursuant to Section 13(a) or 15(d) of the Securities Exchange Act of 1934 are available on our website at www.photomedex.comwww.fcglobalrealty.com as soon as reasonably practicable after we electronically file such reports with, or furnish them to, the SEC. The information on the Company'sour website is not a part of this Annual Report on Form 10-K.

Item 1A.  Risk Factors
ITEM 1A.RISK FACTORS.

In addition to the other information contained in this Annual Reportreport and the exhibits hereto, the following risk factors should be considered carefully in evaluating our business. Our business, financial condition, cash flows or results of operations could be materially adversely affected by any of these risks. Additional risks not presently known to us or that we currently deem immaterial may also adversely affect our business, financial condition, cash flows or results of operations. The following discussion of risk factors contains forward-looking statements as discussed on page 1.above. Our business routinely encounters and addresses risks, some of which may cause our future results to be different – sometimes materially different – than we presently anticipate.

Risk Factors

Risks Relating to Our Business Generally

Our financial condition as of December 31, 2017 raises substantial doubt about our ability to continue as a going-concern.

As of December 31, 2017, we had an accumulated deficit of approximately $134.45 million and shareholders’ deficit of approximately $2.90 million. To date, and subsequent to the Company's Business

The Company isrecent sale of our last significant business unit, we have dedicated most of our financial resources to general and administrative expenses. At present, we are only generating de minimis income from our legacy operating activities.

Cash and cash equivalents as of December 31, 2017 were approximately $0.95 million. We have historically financed our activities with cash from operations, the private placement of equity and debt securities, borrowings under lines of credit and, in default under its senior credit facility,the most recent periods with the sale of certain assets and is currently operating under a forbearance arrangement.

business units.

On May 12, 2014, the CompanyMarch 31, 2017, we entered into an $85 million senior secured credit facilities ("the Facilities") with JP Morgan Chase ("Chase")Contribution Agreement under which included a $10 million revolving credit facility and a $75 million four-year term loan. The facilitiescertain real estate investment properties were utilizedcontributed to refinanceour company in exchange for the existing term debt with Chase, fund the acquisitionissuance of LCA and for workingour capital and other general corporate purposes. The facilities are secured by a first priority security interest in and lien on all assetsstock. Closing of the Company. All currentContribution Agreement occurred on May 17, 2017. However, the assets assumed in such contribution do not represent a business and future subsidiaries are guarantorsnot producing cash flows and/or revenues.

On December 22, 2017, we entered into the Purchase Agreement with OFI, under which OFI may invest up to $15 million in our company in a series of closings, in exchange for which OFI will receive shares of our newly designated Series B Preferred Stock at a purchase price of $1.00 per share. On December 22, 2017, we completed the first closing under the Purchase Agreement, pursuant to which OFI provided $1.5 million to us. On January 24, 2018, we completed a second closing under the Purchase Agreement, pursuant to which OFI provided approximately $2.2 million to us in. Under the Purchase Agreement, OFI may, but is not obligated to, make additional investments in one or more subsequent closings until an aggregate amount of $15 million has been invested or the Purchase Agreement has been terminated in accordance with its terms. OFI has no obligation to continue to invest in our company, and there are restrictions placed by OFI on the facilities.

The credit agreement contains financial covenants including a maximum leverage covenant and a minimum fixed charge covenant which the Company must maintain. These covenants are determined quarterly based on a rolling past four quartersuse of financial data. The Company failed to meet those covenants as of June 30, 2014; On August 4, 2014, the Company received a notice of default and a reservation of rights from Chase and engaged a third-party independent advisor to assist the Company in negotiating a longer term solution to the defaults. The parties had entered into an initial Forbearance Agreement (the "Initial Forbearance Agreement") on August 25, 2014. On November 4, 2014, the Company entered into an Amended and Restated Forbearance Agreement (the "Amended Forbearance Agreement") with the lenders that are parties to the Credit Agreement and with Chase, as Administrative Agent for the Lenders.
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these funds.


Effective February 28, 2015, the Company entered into a Second Amended and Restated Forbearance Agreement (the "Second Amended Forbearance Agreement") with the lenders (the "Lenders") that are parties to the Credit Agreement dated May 12, 2014, and with JP Morgan Chase, as Administrative Agent for the Lenders.
Pursuant to the terms of the Second Amended Forbearance Agreement, the Lenders have agreed to forbear from exercising their rights and remedies with respect to the Specified Events of Default from August 25, 2014 until April 1, 2016, or earlier if an event of default occurs (the "Forbearance Period"). Chase and the Lenders agreed that the Company shall not be obligated to pay the principal amounts set forth in Section 2.08(b) of the Credit Agreement for any date identified therein during the period beginning on February 28, 2015 and ending on the end of the Forbearance Period (the "Effective Period") and that any failure to do so shall not constitute a default or event of default. Instead, the Lenders and the Company agreed that the Company would make prepayments against the Term Loan of $250,000 on the first business day of each month during the Forbearance Period, which

We will be applied in direct order of maturity. The Company also agreed that, on or before the fifth calendar day of each month, the Company would pay against the Term Loan $125,000required to the extent that the cash-on-hand exceeds $5 million, and 100% of the cash-on-hand in excess of $7 million, also to be applied to the Term Loan in inverse order of maturity.

Under the provisions of the Second Amended Forbearance Agreement, the Company will not have to comply with certain financial covenants contained in Section 6.11 of the Credit Agreement for the Forbearance Period, and that any failure to do so shall not constitute a default or event of default. However, the Company will have to meet certain minimum EBITDA targets (as defined in the forbearance agreement) for the quarters ending March 31, 2015, June 30, 2015, September 30, 2015 and December 31, 2015.
Pursuant to the Second Amended Forbearance Agreement, all loans under the Facilities shall, beginning November 1, 2014, bear interest at the CB Floating Rate (as defined in the Credit Agreement) plus 4.00%. Additionally, following the occurrence and continuance of any default or event of default (other than a Specified Event of Default), the Company's obligations under the Facilities shall, at the option of Chase and the Lenders, bear interest at the rate of 2.00% plus the rate otherwise in effect.
The Company and its subsidiaries have also agreed not to pay in cash any compensation to the either the Company's Chief Executive Officer or President that is based on a percentage of sales or another metric other than those officer's base salary, perquisites and standard benefits provided to or on behalf of those executives under the terms of their employment agreements. Those payments may be accrued or deferred and paid in cash only after the repayment of the Facilities in full.
The Company has agreed to provide, on or before May 29, 2015, a strategic business plan for the overall direction of the Company's and its subsidiaries' businesses, including projected income statements, balance sheets, schedules of cash receipts and cash disbursements, payments and month-end balances, and detailed notes and assumptions, projected on a monthly basis through April 1, 2016. The Company has also agreed to provide quarterly updates to that plan by August 31, 2015, November 30, 2015 and February 29, 2016.
The Company continues to retain the services of both Getzler Henrich & Assoc. LLC, a third-party independent business advisor, as well as Canaccord Genuity, Inc., a banking and financial services company, and has also retained the services of Nomura Securities International, Inc., also a banking and financial services company. During the Forbearance Agreement, the Company and these advisors will continue to prepare and distribute offering memoranda and other marketing materials to prospective lenders with regard to a proposed credit facility for the Company, the proceeds of which would be in an amount sufficient to repay in full and in cash the Company's remaining obligations under the Facilities, and to explore other strategic alternatives. The closing of any such refinancing or alternative arrangement would occur no later than the end of the Forbearance Period.
The Company agreed to limit certain capital expenditures to $100,000 per quarter, except for those involving the Company's XTRAC ® or VTRAC ®  medical devices, and will not make investments or acquire any other interests in affiliated companies except as agreed to by the Lenders.
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As consideration for the Lender's entry into the Second Amended Forbearance Agreement, the Company has agreed to pay the Lenders certain forbearance fees (the "Forbearance Fees"), which are earned on the last business day of each of the specified months: for May and June 2015, $750,000 each month; for July through September 2015, $1,000,000 each month; for October through December 2015, $1,250,000 each month; and for January through March 2016, $1,500,000 each month. However, should the Company complete a capital transaction acceptable to the Lenders that reduces the then-outstanding principal balance of the Term Loan to less than $10 million and repays all Forbearance Fees accrued and unpaid to that date, the monthly Forbearance Fee for the remainder of the Forbearance Period shall be earned and accrued in an amount that is 50% of the amount specified for each of the remaining months. In addition, the $500,000 Forbearance Fee set forth in Section 4.10(b) of the Amended Forbearance Agreement remains due and payable to the Lenders on the earlier of the Expiration Date or the Termination Date of the Forbearance Period. All Forbearance Fees are considered earned and are included in the Obligations under the Credit Agreement.
The Company continues to explore refinancing possibilities as well as other strategic alternativesobtain additional liquidity resources in order to resolve this defaultsupport our operations. We are addressing our liquidity needs by seeking additional funding from lenders and repay the facilities. However, there isinvestors. There are no guaranteeassurances, however, that the Companywe will be able to enter into a refinancing or alternative arrangement in a timely manner or under such terms as are acceptableobtain an adequate level of financial resources required for the short and long-term support of our operations.

These conditions raise substantial doubt about our ability to the Lenders. In the event that the Company is unable to enter into such an acceptable arrangement, or if, by the end of the Forbearance Period, the Company and its Lenders have not entered into another forbearance agreement or otherwise reached an agreement regarding the Credit Agreement and the Facilities, the Lenders have the right to declare all of the obligations under the Credit Agreement and Facilities due and payable, including principal and interest, as authorized by the Credit Agreement, and to enforce additional obligations under the Second Amended Forbearance Agreement. Such a result would have a material adverse effect on the Company and its financial condition.

Economic downturns and disruption in the financial markets could adversely affect the Company's financial condition and results of operations.
Financial markets in the United States, Europe and Asia have experienced significant disruption since 2008, including volatility in securities prices and diminished liquidity and credit availability. Furthermore, the economic slowdown during this period in the United States and other countries has weakened consumer confidence and led to significant reductions in the amounts persons and businesses will spend on consumer products and other expenditures. In part,continue as a going concern. The accompanying consolidated financial statements do not include any adjustments to reflect the possible future effects on recoverability and classification of liabilities that may result certainfrom the outcome of the Company's operations and revenues declined. 
this uncertainty.

If adverse general economic conditions continue, the Company's future revenue, profitability and cash flow from operations could decrease and its liquidity and financial condition could be adversely impacted.

The Company is exposed to credit risk of some of its customers.
Most of the Company's sales related to its no!no!® line of products are on an open credit basis. The Company monitors individual customer payment capability in granting such open credit arrangements, seeks to limit such open credit to amounts the Company believes the customers can pay, and maintains reserves it believes are adequate to cover exposure for doubtful accounts. Beyond its open credit arrangements, the Company has also experienced demands for customer financing and facilitation of leasing arrangements, which it typically refers to leasing companies unrelated to the Company.
The Company's exposure to the credit risks may increase due to the current economic slowdown. Although the Company has programs in place that are designed to monitor and mitigate the associated risk, there can be no assurance that such programs will be effective in reducing its credit risks. Future credit losses, if incurred, could harm its business and have a material adverse effect on its operating results and financial condition. The Company maintains estimated accruals and allowances for its business terms. However, distributors tend to have more limited financial resources than other resellers and end-user customers and therefore represent potential sources of increased credit risk because they may be more likely to lack the reserve resources to meet payment obligations.
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The Company maywe need to raise additional funds to pursue itsour growth strategy or continue itsour operations, and we may be unable to raise capital when needed.

From time to time, the Companywe may seek additional equity or debt financing to make acquisitions or other investments, to provide for the capital expenditures, required to finance working capital requirements, continue itsour expansion, toor increase liquidity, develop new products and services or make acquisitions or other investments.liquidity. In addition, if itsour business plans change, general economic, financial or political conditions in itsour markets change, or other circumstances arise that have a material negative effect on itsour cash flow, the anticipated cash needs of itsour business as well as itsour conclusions as to the adequacy of itsour available sources of capital could change significantly.

Any of these events or circumstances could result in significant additional funding needs, requiring the Companyus to raise additional capital, and we cannot predict the timing or amount of any such capital requirements at this time. If financing is not available on satisfactory terms, or at all, the Companywe may be unable to expand its business or to develop newour business at the rate desired and itsour results of operations may suffer.

If

We are dependent upon dividends from our subsidiaries to meet our financial obligations.

We are a holding company and our principal assets are the Company does not continue to develop and commercialize new products and identify new markets for its products and technologies, the Company may not remain competitive, and its revenues and operating results could suffer.

The cosmetic industry is subject to continuous technological development and product innovation. If the Company does not continue to innovateequity interests we hold in developing new cosmetic products and applications, its competitive position will likely deteriorate as other companies successfully design and commercialize new products and applications. Accordingly, its success depends in partour subsidiaries, which own, either directly or indirectly through their subsidiaries, our real estate assets. As a result, we depend on developing innovative applications of its technology and identifying new markets for, and applications of, existing products and technology. While the Company has reduced its cosmetic research and development expenditures in an effort to focus its resources on selling and marketing its existing no!no!® line of products, if the Company is unable to develop and commercialize new cosmetic products and identify new markets for such products and technology, its cosmetic products and technology could become obsolete and the Company's revenues and operating results could be adversely affected.
The markets for the Company's products are intensely competitive and we may not be able to compete effectively against the larger, more well-established companies that dominate this market or emerging, and small, innovative companies that may seek to obtain or increase their share of the market.
The markets for the Company's products are intensely competitive and many of our competitors are much larger and have substantially more financial and human resources than we do. Many have long histories and strong reputations within the industry and a relatively small number of companies dominate these markets.
Our no!no!® hair removal products compete directly with branded, premium retail products such as Philips and Braundividends and other light based products of public companies such as Syneron, Valeantpayments from our subsidiaries to generate the funds necessary to meet our financial obligations. Our existing subsidiaries are legally distinct from us and Cynosure.may be significantly restricted from paying dividends or otherwise making funds available to us pursuant to the agreements governing their financing arrangements. In addition, due to regulatory restrictions concerning claims about the efficacy of personal care products, we may have difficulty differentiating our products from other competitive products, and competing products entering the personal care market could harm our revenue. Also, our no!no!® line of products are energy based. As such, energy-based aesthetic products may face competition from non-energy-based medical products, such as Botox, an injectable compound used to reduce wrinkles and collagen injections. Other alternatives to the use of our no!no!® line of products include electrolysis, a procedure involving the application of electric current to eliminate hair follicles and chemical peels. In addition, we may also face competition from manufacturers of other products that have not yet been developed.
We also face direct competition from large pharmaceutical companies, including, for example, Biogen, Inc., Centocor, Inc., and Abbott Laboratories, which are engaged in the research, development and commercialization of treatments for psoriasis, atopic dermatitis, vitiligo and leukoderma. In some cases, those companies have already received FDA approval or commenced clinical trials for such treatments. Many of these companies have significantly greater financial resources and expertise in research and development, manufacturing, conducting pre-clinical studies and clinical trials and marketing than we do.
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Other competitors include well-established pharmaceutical, cosmetic and healthcare companies such as Allergan, Inc., Valeant Pharmaceuticals International, Inc and Estee Lauder Inc. These companies may enjoy significant competitive advantages over us, including:
broad product offerings, which address the needs of physicians and hospitals in a wide range of procedures;
greater experience in, and resources for, launching, marketing, distributing and selling products, including strong sales forces and established distribution networks;
existing relationships with physicians and hospitals;
more extensive intellectual property portfolios and resources for patent protection;
greater financial and other resources for product research and development;
greater experience in obtaining and maintaining FDA and other regulatory clearances or approvals for products and product enhancements;
established manufacturing operations and contract manufacturing relationships;
significantly greater name recognition and more recognizable trademarks; and
established relationships with healthcare providers and payors.
Smaller or early-stage companies may also prove to be significant competitors, particularly through collaborative arrangements with large and established companies. Our commercial opportunity will be reduced or eliminated if we are unsuccessful in convincing physician and patient customers and consumers to use our products or if our competitors develop and commercialize products that are safer and more effective than any products that we may develop.
Because a substantial portion of the Company's revenue is generated from its consumer business, if it fails to accurately forecast consumer demand and trends in consumer preferences, or if there is a decline in discretionary consumer spending, then the Company's revenues and profitability could decline.
Consumers in the aesthetic and skincare products industry have tastes, preferences and loyalties that are subject to change. If we do not keep up with consumer preferences and trends, or if we do not accurately forecast such preferences and trends, sales revenues in the Company's consumer business may decline or our reputation may suffer. The success of our consumer product business depends to a significant extent upon discretionary consumer spending, which is subject to a number of factors, including general economic conditions, consumer confidence, employment levels, business conditions, interest rates, availability of credit, inflation and taxation. Adverse trends in any of these economic indicators may cause consumer spending to decline further, which could hurt its sales and profitability.
The Company's laser treatments of psoriasis, vitiligo, atopic dermatitis and leukoderma, the Company's skincare products and its PTL (Photo Therapeutics Ltd.) products and any of the Company's future products or services may fail to gain market acceptance, which could adversely affect the Company's competitive position.
The Company has generated limited commercial distribution for its XTRAC system and certain of its other products. It is still not established that the PTL devices targeted for the consumer market will be widely accepted in that market. The Company may be unsuccessful in continuing its existing or developing new, strategic selling affiliates and alternate channels in order to maintain or expand the markets for the existing or future products of the skincare and PTL businesses.
Even if adequate financing is available and such products are ready for market, the Company cannot assure you that its products and services will find sufficient acceptance in the marketplace under its sales strategies.
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The Company also faces a risk that other companies in the market for dermatological products and services may be able to provide dermatologists a higher overall yield on investment and therefore compromise the Company'stheir ability to increase its base of usersmake payments to us will also depend on their earnings, business, tax considerations and ensure they engage in optimal usage of its products. If, for example, such other companies have products (such as Botox or topical creams for disease management) that require less time commitment from the dermatologist and yield an attractive return on a dermatologist's time and investment, we may find that our efforts to increase our base of users are hindered.
While the Company has engaged in clinical studies for its psoriasis treatment and, based on these studies, it has gained FDA clearance, appropriate Current Procedural Terminology, or CPT, reimbursement codes for treatment and suitable reimbursement rates for those codes, from the Centers for Medicare & Medicaid Services, or CMS, we may face other hurdles to market acceptance. For example, practitioners in significant numbers may wait to see longer-term studies; or it may become necessary to conduct studies corroborating the role of the XTRAC system as a first-line or second-line therapy for treating psoriasis; or patients simply may not elect to undergo psoriasis treatment using the XTRAC system.
Beginning in early 2010, Dr. John Y.M. Koo, the director of the Psoriasis Treatment Center at the University of California San Francisco Medical Center, initiated a clinical study to demonstrate the effectiveness of the XTRAC Velocity in combination with the drugs Clobex® and Vectical®, both from Galderma, for patients with severe psoriasis. This study may or may not result in demonstrating the effectiveness of those products in combination, or the treatment protocol and the treatment protocol may or may not gain FDA clearance. Even if the treatment protocol is successful and gains FDA clearance, limitation of supply of one or both drugs by Galderma, and lack of viable substitutes therefore, may adversely impact use of or compliance with the treatment protocol as a therapy for treatment of psoriasis. Further, the FDA limits claimed indications for use to those found in the "Instructions for Use Statement" in a device's 510(k) clearance letter. The FDA may view certain of the Company's claims of treatment as outside the scope of the device's cleared indications for use.
If the FDA determines that the clinical studies were not conducted in accordance withlegal restrictions, including applicable FDA requirements, the FDA could take regulatory and/or legal enforcement actions against the Company and/or its products and could attempt to withdraw premarket 510(k) clearance.
Whether a treatment may be delegated and, if so, to whom and to what extent, are matters that may vary state by state, as these matters are within the province of the state medical boards. In states that may be more restrictive in such delegation, a physician may decline to adopt the XTRAC system into his or her practice, deeming it to be fraught with too many constraints and finding other outlets for the physician's time and staff time to be more remunerative. There can be no assurance that the Company will be successful in persuading such medical boards that a liberal standard for delegation is appropriate for the XTRAC system, based on its design for ease and safety of use. If the Company is not successful, it may find that even if a geographic region has wide insurance reimbursement, the region's physicians may decline to adopt the XTRAC system into their practices.
The Company thereforecorporate laws. We cannot assure you that the marketplaceagreements governing our current and future indebtedness of our subsidiaries, applicable laws or state regulation will permit our subsidiaries to provide us with sufficient dividends, distributions or loans to fund payments to meet our financial obligations.

If we fail to manage our growth effectively, our businesses could be receptive to its excimer laser technology or skincare products over competing products, services and therapies or that a cure will not be found for the underlying diseases the Company is focused on treating. Failure of the Company's products to achieve market acceptance could have a material adverse effect on the Company's business, financial condition and results of operations.

The success of the Company's XTRAC system and other treatment products depends on third-party reimbursement of patients' costs,disrupted which could resultharm our operating results.

We expect to experience growth in potentially reduced prices or reduced demandour business, both organically and in relevant part, adversely affect the Company's revenuesthrough acquisitions. We expect to make significant investments to enable our future growth. Such growth may place a strain on our management and business operations.

The Company's Our ability to market the XTRAC system and other treatment products successfullymanage this growth will depend in large part onupon, among other factors, our ability to broaden our management team; our ability to attract, hire, train, motivate and retain skilled employees; and the extent to which various third parties are willing to reimburse patients or providers for the costsability of medical procedures utilizing such products. These third parties include government authorities, private health insurersour officers and other organizations, such as health maintenance organizations, whose patterns of reimbursement may change as a result of new standards for reimbursement determined by these third parties or because of the programs and policies enacted under the Patient Protection and Affordable Care Act of 2010.
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Third-party payors are systematically challenging the prices charged for medical products and services. They may deny reimbursement if they determine that a prescribed device is not used in accordance with cost-effective treatment methods as determined by the payor, or is experimental, unnecessary or inappropriate. Further, although third parties may approve reimbursement, such approvals may be under terms and conditions that discourage use of the XTRAC system. Accordingly, if less costly drugs or other treatments are available, third-party payors may not authorize or may limit reimbursement for the use of the Company's products, even if its products are safer or more effective than the alternatives.
In addition, medical insurance policies and treatment coverage have been and may be affected by the parameters of the Patient Protection and Affordable Care Act of 2010. While the Act's stated purpose is to expand access to coverage, it also mandates certain requirements regarding the types and limitations of insurance coverage. There can be no guarantee that the changes in coverage under the Act will not affect the type and level of reimbursement for our products.
Although the Company has received reimbursement approvals from a majority of private healthcare plans, we cannot give assurance that these private plans will continue to adopt or maintain favorable reimbursement policies or accept the XTRAC system in its clinical role as a second-line therapy in the treatment of psoriasis. Additionally, third-party payors may require further clinical studies or changes to the Company's pricing structure and revenue model before authorizing or continuing reimbursement.
As of December 31, 2014, the Company estimates, based on published coverage policies and on payment practices of private and Medicare insurance plans, that more than 90% of the insured population in the U.S. is covered by insurance coverage or payment policies that reimburse physicians for using the XTRAC system for treatment of psoriasis. Based on these reports and estimates, the Company is continuing the implementation of a roll-out strategy under revised user models for the XTRAC system in the U.S. in selected areas of the country where reimbursement is widely available. The success of the roll-out depends on increasing physician and patient awareness and demand for the treatment. The Company can give no assurance that health insurers will not adversely modify their reimbursement policies for the use of the XTRAC system in the future.
The Company intends to seek coverage and reimbursement for the use of the XTRAC system to treat other inflammatory skin disorders after additional clinical studies are initiated. There can be no assurances that the Company will be in a positionkey employees to continue to expand coverage for vitiligo or to seek reimbursement for the use of the XTRAC system to treat atopic dermatitis or leukoderma, or, if the Company does, that any health insurers will agree to any reimbursement policies.
implement and improve our operational, financial and other systems. Our future success is heavily dependent upon achieving such growth. Any failure in our customer education efforts could significantly reduce product marketing.
It is important to the success of our marketing efforts to educate physicians and technicians how to properly use the XTRAC system. We rely on physicians to spend their time and money to participate in our pre-sale educational sessions. Moreover, if physicians and technicians use the XTRAC system improperly, they may have unsatisfactory patient outcomes or cause patient injury, which may give rise to negative publicity or lawsuits against us, any of whicheffectively manage future growth could have a material adverse effect on our reputation, revenues and profitability.
Many of the Company's expenses are fixed and many are based, in significant part, on its expectations of its future revenue and are incurred prior to the sale of its products and services. Therefore, any significant decline in revenue for any period could have an immediate negative impact on its margins, net income and financial results for the period.
The Company's expense levels are based, in significant part, on its estimates of future revenue and many of these expenses are fixed in the short term. As a result, the Company may be unable to adjust its spending in a timely manner if its revenue falls short of its expectations. Accordingly, any significant shortfall of revenue in relation to its estimates could have an immediate negative effect on its profitability. In addition, as its business, grows, the Company anticipates increasing its operating expenses to expand its product development, technical support, sales and marketing and administrative organizations. Any such expansion could cause material losses to the extent the Company does not generate additional revenue sufficient to cover the additional expenses.
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If revenue from a significant customer declines, the Company may have difficulty replacing the lost revenue, which would negatively affect its results and operations.
Excluding niche marketing efforts, the Company's skincare business targets its sales in the U.S. market to physicians, who then mark up the products for sale to their patients. No single physician practice in itself is generally responsible for a significant proportion of the Company's sales. The Company finds as well that a few physicians re-sell our products not just to their own patients, but also at discounted prices on the internet. These practices undercut the sales of other physicians and violate the Company's internet sales policy; while the Company has taken steps to prevent these practices,  this policy can be difficult to enforce.
In its international businesses, the Company depends for a material portion of its sales in the international arena on several key sub-distributors, and especially on The Lotus Global Group, Inc., doing business as GlobalMed Technologies Co., or GlobalMed, which is the Company's master distributor over most of the international arena for our devices (excluding our no!no!® line of products). If the Company loses GlobalMed or one of these sub-distributors, the Company's sales of phototherapy and surgical lasers are likely to suffer in the short term, which could have a negative effect on its revenues and profitability.
In addition to its sales through online and infomercial outlets, the Company's no!no! brand products are also marketed through certain major retailers, including HSN, Nordstrom's and Bed, Bath and Beyond. None of these retailers accounts for more than 10% of the sales of this product line in the United States. However, the loss of one or more of these retailers, without replacement by a comparable sales channel, could have a near-term impact on sales of the no!no! products and an effect on the Company's revenues and profitability.
The Company's failure to maintain its relationships with its key distributors (none of which have an ongoing obligation to sell our products) on acceptable terms would have a material adverse effect on its results of operations and financial condition, or if the Company fails to effectively manage or, retain its distribution network or its sales force, its business, prospects and brand may be materially and adversely affected.
Sales made through retailers and distributors constitute a significant part of the Company's sales revenue. These retailers and distributors are not obligated to sell its products, and may choose to end their relationship with us. Even ifcondition.

We have outstanding litigation which we maintain a business relationship with such retailers and distributors, they may sell competing products or may not be able to sellsettle, or which we may not be able to settle on terms favorable to us.

We are involved in certain litigation relating to our products. Maintainingformer businesses, including a two product liability suits brought by a consumer regarding the no!no! product. We intend to vigorously defend claims brought against us, and to prosecute such suits to recoup sums owed to us. However, we may seek to settle such matters in order to avoid excessive legal fees and costs and the lengthy time such litigation may require in order to reach a resolution. However, there is no guarantee that we may be able to reach a settlement or resolution of such litigation, or that such a settlement or resolution will be reached in a manner that is advantageous to us, and in such cases we will need to proceed with litigation. Regardless of its outcome, litigation may result in substantial costs and expenses, and significantly divert the attention of management. There can be no assurance that we will be able to prevail in, or achieve a favorable settlement of, pending matters. In addition to the pending matters, future litigation, government proceedings, labor disputes, or environmental matters could lead to increased costs or interruption of our normal business relationships with these retailersoperations, which could involve a costly and distributorslengthy draw upon our resources and their continued successcould result in a resolution to the litigation which may be detrimental to us.


We are the subject of certain tax audits which may not be resolved without impacting our operations.

We have in the past, and are currently, the subject of certain audits by state agencies and international authorities for various tax matters including, but not limited to, sales and use and corporate income taxes, and unclaimed property reporting. While past audits have been resolved without significant impact upon us or our operations, there is importantno guarantee that future audits will be resolved in a manner that is satisfactory to maintainingus or that has no material impact upon our operations. Such results could include the Company's revenuespayment of assessments which could impact our remaining resources and profitability.

Furthermore, the Company has a limitedaffect our ability to managecontinue our operations in the activitiesexisting manner.

We depend on our executive officers and key personnel to implement our business strategy and could be harmed by the loss of its independent third-party distributors.their services and the inability to attract personnel for these positions.

We believe that our growth and future success will depend in large part upon the skills of our key management. Certain members of our management staff as well as other key employees may voluntarily terminate their employment with us at any time, with or without notice. There is substantial competition for personnel in the industries in which we operate, and we may face increased competition for such employees, resulting in the need to compensate these personnel at a higher-than-anticipated rate, a delay in replacing such personnel and integrating them into our operations, and the possibility that we may be unable to attract and retain these personnel. The Company's distributors could take one or moreloss of the following actions, anyservices of which could have a material adverse effect on its business, prospects and brand:

sell products that compete with its products in breach of their non-competition agreements with the Company;
violate laws or regulations;
fail to adequately promote its products; or
fail to provide proper service to its retailers or end-users.
Failure to adequately manage the Company's distribution network,key personnel, or the non-compliance of this network with its obligations under agreements with us,inability to attract and retain additional qualified personnel, could harm the Company's corporate image among end users of its products and disrupt its sales, or result in finesdelays to product development or other legal action against the Company.
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The Company does not currently have a distributor in the Japanese market, and the failure to identify a new distributor or another long-term methodapproval, loss of sales in this marketand diversion of management resources, and may have an adverse effect on its business.
On November 21, 2013 the Company's majority-owned subsidiary, Radiancy, Inc., terminated the exclusive distribution agreement between itself and Ya-Man Ltd., Radiancy's independent distributor for the no!no!® brand products in the Japanese market. Sales in Japan represented approximately 5% of the revenues related to the sale of the no!no! products for the year ended December 31, 2013; those sales were largely generated in the first six months of the year. Ya-Man failed to meet its minimum purchasing commitments under the distribution agreement in the third and fourth quarters of 2013, due to a restructuring of its methods of business operations. Radiancy and Ya-Man also disputed the responsibility for the payment of marketing expenses for that country of approximately $1 million.
The Company and Radiancy continue to seek a new distribution partner for the Japanese markets while exploring other options in which to continue the sale of products in Japan, including the use of other methods of third-party marketing and sale or the formation of an office in Japan to directly market these products. Meanwhile, retail sales to consumers of the no!no! brand products remain strong, and Ya-Man has continued to market and sell its inventory of those products in Japan. However, the Company has no assurance that a new distributor will purchase these products at the same levels as Ya-Man, will purchase the Company's new products, or that an agreement with a new distributor will be made on the same terms as the previous agreement with Ya-Man, or at all. The Company also has no assurance that the use of other third-party marketing outlets, or the formation of an office of Radiancy in Japan to directly market these products, will result in the same level of sales as that generated through the distributorship of Ya-Man. The potential diminution or loss of this market may result in lower sales and profits. If the Company is unable to replace these sales, either through a distributor or other arrangement of sale in Japan or through sales made in other markets, that loss may have an adverse material negative effect on its future operating results.
Other factors that could impact the Company's results in the market include:
increased regulatory constraints with respect to the claims the Company can make regarding the efficacy of products and tools, which could limit its ability to effectively market them;
an adverse impact on the Japanese economy and impairment of consumer spending as a result of the future earthquakes, tsunami and other natural disasters in Japan;
significant weakening of the Japanese yen;
continued or increased levels of regulatory and media scrutiny and any regulatory actions taken by regulators, or any adoption of more restrictive regulations, in response to such scrutiny; and
increased competitive pressures from other home use aesthetic device companies who actively seek to solicit its distributors to join their businesses.
A number of the Company's product sales depend on search engines and other online sources to attract visitors to its websites, and if the Company is unable to attract these visitors and convert them into customers in a cost-effective manner, itsour business and financial results may be harmed.
A major part of the Company's direct response campaign for its no!no!® line of products' success depends on itsour ability to attract online consumers to its websites and convert them into customers in a cost-effective manner, whichgrow that business.

In particular, our success depends in part on search engines and other online sources for its website traffic. Our subsidiary's name, Radiancy, as well as the name of our flagship products, no!no!, and variations of those names, are included in search results as a result of both paid-search listings, where the Company purchases specific search terms that will result in the inclusion of its listing, and algorithmic searches that depend upon the searchable content on its sites. Search enginescontinued service and other online sources revise their algorithms from time to time in an attempt to optimize their search results.

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If one or moreperformance of Mr. Vineet P. Bedi, our Chief Executive Officer, and Mr. Matthew Stolzar, our Chief Financial Officer and Chief Investment Officer. We have fixed-term employment agreements with Messrs. Bedi and Stolzar; however, there are no assurances that the search engines or other online sources on which the Company relies for website traffic were to modify its general methodology for how it displays its websites, resulting in fewer consumers clicking through to its websites, the Company's sales could suffer. If any free search engine on which the Company relies begins charging fees for listing or placement, if one or moreservices of the Company's competitors outbids the Company for specific search terms or utilizes search terms which are similar to those purchased by the Company, or if one or more of the search engines or other online sources on which it relies for purchased listings, modifies or terminates its relationship with the Company, its expenses could rise, it could lose customers, and traffic to its websites could decrease.
We generate our consumer revenues almost entirely from advertising, and the reduction in availability of such advertising or loss of advertising outlets could seriously harm our business.

We generate a significant portion of the sales of our no!no! Hair and skin consumer products through the use of advertising, including online, over-the-air and direct-to-market programs. Over the past year, the market for such advertising has undergone major and unanticipated changes, resulting in lowered availability of advertising airtime and higher prices for the available airtime.  As a result, we have been unable to purchase the same level of advertising as wasthese individuals will be available to us for any specified period of time. The loss of the services of one or both of these officers could adversely affect our ability to develop and expand our business.

Additionally, we do not currently maintain “key person” life insurance on the lives of Messrs. Bedi and Stolzar, our other executives or any of our employees. Our lack of insurance means that we may not have adequate compensation for the loss of the services of our key employees, which could affect our ability to maintain the level of services formerly provided by those persons.

In our industry, there is substantial competition for key personnel in the past, resultingregions in less sales leads, a lower-rate-of-return on our advertising spendwhich we operate and a lower level of saleswe may face increased competition for these products.

such employees. If we are unable to purchaseattract key personnel in a timely manner, including key personnel who have critical industry experience and relationships in the regions in which we operate, it may have an appropriate level of advertising time, deliver our advertising in an appropriate and effective manner, and/or reach an acceptable rate of return on our advertising spend, we will continue to receive lower levels of sales leads and ultimately customers, and will generate less revenue in these product lines, which could have a material impactadverse effect on our business and our revenues.

The Company'sability to drive growth.

Our ability to use our net operating resultsloss carryforwards to offset future taxable income for U.S. federal income tax purposes may be limited as a result of “ownership changes” of our company caused by the Contribution Transaction. In addition, the amount of such carryforwards could be negatively impactedsubject to adjustment in the event of an examination by economic, political or other developments in foreign countries in which it or its subsidiaries do business.

The Company transports some of its goods across international borders, primarily thosethe Internal Revenue Service.

If a corporation undergoes an “ownership change” under Section 382 of the U.S., Canada, Europe, Japan and Israel. Since September 11, 2001, there has been more intense scrutinyInternal Revenue Code of goods that are transported across international borders. As a result, some of our and our subsidiaries' products may face delays, and increase in costs due to such delays in delivering goods to its customers. Any events that interfere with,1986, as amended, or increase the costs of the transfer of goods across international borders, could have a material adverse effect on its business.

Further, global economic conditions continue to be challenging. Although the economy appears to be recovering in some countries, it is not possible for us to predict the extent and timing of any improvement in global economic conditions. Even with continued growth in many of our and our subsidiaries' markets during this period, the economic downturn could adversely impact its business in the future by causing a decline in demand for our and our subsidiaries' products, particularly if the economic conditions are prolonged or worsen.
The international nature of the Company's business exposes us to certain business risks that could limit the effectiveness of the Company's growth strategy and cause our results of operations to suffer.
Continued expansion into international markets is an element of the Company's growth strategy. Introducing and marketing the Company's services internationally, developing direct and indirect international sales and support channels and managing foreign personnel and operations will require significant management attention and financial resources. The Company faces a number of risks associated with expanding the Company's business internationally that could negatively impact the Company's results of operations, including:
management, communication and integration problems resulting from cultural differences and geographic dispersion;
compliance with foreign laws, including laws regarding manufacture, importation and registration of products;
compliance with foreign regulatory requirements and the ability of GlobalMed to establish additional regulatory clearances necessary to expand distribution of the Company's products in countries outside of the United States;
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competition from companies with international operations, including large international competitors and entrenched local companies;
difficulties in protecting and enforcing intellectual property rights in international jurisdictions, including against persons and companies which offer counterfeit copies of our products;
political and economic instability in some international markets;
sufficiency of qualified labor pools in various international markets;
currency fluctuations and exchange rates; and
potentially adverse tax consequences or an inability to realize tax benefits.
The Company may not succeed in its efforts to expand its international presenceCode, as a result of the factors described aboveacquisition, the amount of our pre-change net operating losses, or NOLs, that may be utilized to offset future taxable income will be subject to an annual limitation. In general, an ownership change occurs if the aggregate stock ownership of certain stockholders increases by more than 50 percentage points over such stockholders’ lowest percentage ownership during the applicable testing period (generally three years). The annual limitation generally is determined by multiplying the value of the corporation’s stock immediately before the ownership change by the applicable long-term tax-exempt rate. Any unused annual limitation may, subject to certain limits, be carried over to later years, and the limitation may under certain circumstances be increased by recognized built-in gains or reduced by recognized built-in losses in the assets held by the corporation at the time of the ownership change. Similar rules and limitations may apply for state income tax purposes.

Our NOLs, which for federal income tax purposes expire over the next 20 years, may be subject to an annual limitation under Section 382 of the Code as a result of the completion of the Contribution Transaction. Consequently, our ability to utilize our pre-change NOLs may be subject to an additional layer of limitations imposed by Section 382 of the Code. The amount of the NOL carryforwards is subject to review and audit by the Internal Revenue Service and there can be no assurance that the benefit of such NOL carryforwards will be fully realized.


We are analyzing the tax implications of the ownership of our inactive subsidiaries in Israel and Europe, including the tax implications of dissolving or otherwise disposing of such subsidiaries. As a result of the application of Israeli and/or European tax laws, the dissolution or other factors thatdisposition of these subsidiaries may have an adverse impact on the Company's overall financial condition and results of operations. In addition, the Company hasresult in a relationship with GlobalMed, whereby it provides the Company with certain non-U.S. regulatory support. To the extent that the Company discontinues its relationship with GlobalMed, or if GlobalMed is otherwise unable to provide the Company with the resources and assistance that the Company needs, the Company may have a difficult time expanding into international marketssignificant tax in an effective manner.

Conditions in Israel affect our operations related to our no!no!® line of products and may limit the Company's ability to produce and sell its products.
Radiancy, Inc. is a majority owned subsidiary of the Company and the marketer of the Company's no!no! consumer products division. All of Radiancy's research and development activities, a portion of the manufacturing operations and other critical business activities are located in Israel, a country that has experienced terrorist attacks. Political, economic and military conditions in Israel could adversely affect its operations, including a disruption of such operations due to terrorist attacks or other hostilities. Although the current hostilities in Israel have had no immediate and direct impact on Radiancy to date, the interruption or curtailment of trade between Israel and its trading partners, foreign jurisdictions and/or a significant downturntax in the economicUnited States which may not be covered by our NOLs or financial conditionresult in the loss of our NOLs.

Certain of our subsidiaries, both in the United States and in foreign jurisdictions, are participants in intercompany loans which originated at one of the foreign jurisdiction subsidiaries. The foreign subsidiaries could incur a tax liability as a result of holding those open loans. The subsidiary companies are not in a position to repay those loans in full. We and our subsidiaries’ boards are examining how best to proceed, but to either repay a loan, or to default and have the loan forgiven, could result in income being imputed to that subsidiary in the United States. While we and various subsidiaries hold large amounts of NOLs on a Federal level, the use of certain of those losses is restricted under Section 382 of the Code as a result of past changes of control of our company, and the transactions which occurred during 2017 may impose further restrictions on the use of these NOLs should those transactions have resulted in a change of control during 2017. Accordingly, we may be subject to significant and unexpected tax liability in Israel, may adversely affectEurope and/or the flow of vital components from our Israeli subcontractors to us. We cannot assure you that ongoing hostilities related to Israel will notUnited States and such liability would have a material and adverse effect on our businessfinancial condition and prospects.

The Contribution Transaction may not qualify for special tax treatment, for example, as a tax-free reorganization for U.S. federal income tax purposes, resulting in certain stockholders’ recognition of taxable gain or our share price.

The Company's Israeli-based facilities and/or manufacturing subcontractors could also be subjectloss in respect of their stock.

There is currently no opinion as to catastrophic loss suchwhether the Contribution Transaction will qualify for special tax treatment, as, fire, flood, or earthquake. Any such loss at any of these facilities could disrupt operations, delay production, shipmentsfor example, a tax-free reorganization for U.S. federal income tax purposes. Moreover, there is no requirement we take all actions to ensure that the Contribution Transaction so qualifies and, revenue and result in significant expense to repair and replace those facilities.

The operations of the Company's subsidiary Radiancy (Israel) Ltd. may be disrupted by the obligation of its personnel to perform military service.
Many of the Company's employees that are located in Israel are legally obligated to perform annual military reserve duty in the Israeli Defense Forces and may be called to active duty under emergency circumstances at any time without substantial notice to the Company. If a military conflict or war arises, these individuals could be required to serve in the military for extended periods of time. As a result, our Israeli-based operations could be disrupted by the absence, for a significant period of time, of one or more of its executive officers or a significant number of its other employees due to such reserve duty.
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If the Company fails to manage its sales and marketing force or to market and distribute its products effectively, the Company may experience diminished revenues and profits.
There are significant risks involved in building and managing the Company's sales and marketing force and marketing its products, including the Company's ability:
to hire, as needed, a sufficient number of qualified sales and marketing personnel with the aptitude, skills and understanding to market its XTRAC systems, its no!no! Hair and skin products, its skincare lines, its Omnilux and Mistral product lines and its surgical products effectively;
to adequately train its sales and marketing force in the use and benefits of all its products and services, thereby making them more effective promoters;
to manage its sales and marketing force and its ancillary channels (e.g., telesales) such that variable and semi-fixed expenses grow at a lesser rate than its revenues;
to set the prices and other terms and conditions for treatments using the XTRAC system in a complex legal environment so that they will be accepted as attractive skin health and appropriate alternatives to conventional modalities and treatments; and
to cope with employee turnover among the sales force in the skin health business, in which there is substantial competition for talented sales representatives.
To increase acceptance and utilization of its XTRAC system, the Company may have to expand its sales and marketing programs in the U.S. While the Company may be able to draw on currently available personnel within its organization to meet this need, the Company also expects that it will have to increase the number of representatives devoted to the sales and marketing programs and to broaden, through such representatives, the talents it has at its disposal. In some cases, the Company may look outside its organization for assistance in marketing its products.
In similar fashion, the Company cannot predict how successful it may be in marketing its skin health, hair care and wellness products in the U.S., nor can the Company predict the success of any new skin health and hair care products that it may introduce. Despite an increased focus on developing alternate channels for many of the Company's skin health, hair care, and wellness products, the Company may find that channels that are attractive to the Company are unavailable because they already carry competitive products. Notherefore, no assurance can be given that the CompanyContribution Transaction will be successful in marketing and selling its skin health, hair care, and wellness products.
The Company may be unsuccessful in accessingqualify for any certain tax treatment, including as a tax-free reorganization, or that the home-use consumer market with its skin health, hair care, and wellness products. Distribution throughInternal Revenue Service or the consumer marketcourts will be principally through mass-retail chains and e-commerce and electronic media. Whilenot assert that the Company expects the volumes will be higher, the margins may be lower. It may also prove difficultContribution Transaction fails to obtain long-term commitments from the retailers.qualify as such. If the Company is unable to secure distribution partners or obtain favorable pricing or long-term commitments, the Company's efforts in the home-use consumer market may be unsuccessful.
The Company may encounter difficulties in quality testing and the manufacturingContribution Transaction does not qualify as a tax-free reorganization, some holders of its products in commercial quantities, which could adversely impact the rate at which the Company grows.
There can be no guarantee that the Company's quality assurance testing programs will be adequate to detect all defects, either ones in individual products or ones that could affect numerous shipments, which might interfere with customer satisfaction, reduce sales opportunities, or affect gross margins. In the future, the Company may need to replace certain of its no!no!® product's components and provide remediation in response to the discovery of defects or bugs in such products that it has shipped. There can be no assurance that such a remediation, depending on the product involved, would not have a material impact. An inability to cure a product defect could result in the failure of a product line, temporary or permanent withdrawal from a product or market, damage to its reputation, inventory costs or product reengineering expenses, any of which could have a material impact on the Company's revenue, margins and net income.
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Further, the Company may encounter difficulties manufacturing its line of products because it has limited experience manufacturing such products in significant commercial quantities. As a result, the Company will, in order to increase its manufacturing output significantly, have to attract and retain qualified employees for such assembly and testing operations.
Some of the components necessary for the assembly of the Company's products are currently provided to the Company by third-party suppliers. While alternative suppliers exist and could be identified, the disruption or termination of the supply of components could cause a significant increase in the costs of these components, which could affect our operating results. The Company's dependence on a limited number of third-party suppliers and the challenges the Company may face in obtaining adequate supplies involve several risks, including limited control over pricing, availability, quality and delivery schedules. A disruption or termination in the supply of components could also result in the Company's inability to meet demand for its products, which could harm its ability to generate revenues, lead to customer dissatisfaction and damage its reputation. Furthermore, if the Company is required to change the manufacturer of a key component of its products, the Companystock may be required to verify that the new manufacturer maintains facilities and procedures that comply with quality standards and with all applicable regulations and guidelines including Quality Systems Regulations,recognize gain or QSR requirements and performance standards. Failure to do so couldloss or incur other taxable consequences as a result in the FDA taking legal or regulatory enforcement action against the Company and/or its products (e.g. recalls, fines, penalties, injunctions, seizures, prosecution or other adverse actions). The delays associated with the verification of a new manufacturer could delay the Company's ability to manufacture its products in a timely manner or within budget. The Company faces the risk that there will be supply chain problems if the volumes do not match to the margins, as certain of the Company's consumer market products are intended to be high-volume, lower-margined products.
Although the Company believes that its current manufacturing facilities are adequate to support its commercial manufacturing activities for the foreseeable future, the Company may be required to expand or restructure its manufacturing facilities to increase capacity substantially. In addition, if the Company is unable to provide customers with high-quality products in a timely manner, the Company may not be able to achieve market acceptance for its XTRAC system or achieve market acceptance and growth for its skincare products. The Company's inability to manufacture or commercialize its devices successfully could have a material adverse effect on its revenue.
Contribution Transaction.

If the Company fails to manage and protect its and its subsidiaries'subsidiaries’ network security and underlying data effectively, its businesses could be exposed to a cyber-attack or other disruption which could harm its operating results.

Like other large corporations, the Company relies upon a variety of information technology systems to transmit, process and store information in an electronic format for use in daily operations. In particular, the Company possesses and uses both personal health information and personal identification information in the conduct of its business, including credit card, insurance and banking information of our customers.customers and vendors. The size, inter-relationship and complexity of these systems, and the possession of such information, makes us vulnerable to a cyber-attack, malicious intrusion, breakdown, destruction, theft or loss of data privacy or other significant interference with the use and possession of such information, that could harm our business. Unauthorized disclosure or manipulation of such data, whether through breach of network security or other interception of this information, could expose the Company to costly litigation, damage its reputation and result in a lower revenue stream and the loss of some of its customers.

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greater expenses.

Our information systems require a constant and ongoing dedication of significant resources to maintain, protect, and enhance our existing systems as well as keep pace with changes in information processing technology and regulatory standards. In particular, maintaining the Company'sCompany’s network security is of critical importance because the online e-commerce systems used by our consumer product linesmay store proprietary and confidential customer and vendor data such as names, addresses, other personal information, bank account and credit card numbers. The Company uses commercially available encryption technology to transmit personal information when taking orders. However, third parties may be able to circumvent these security and business measures by developing and deploying viruses, worms and other malicious software programs that are designed to attack or attempt to infiltrate its systems and networks. Employee error, malfeasance or other mistakes in the storage, use or transmission of personal information could result in a breach of customer or employee privacy. The Company employs contractors and temporary and part-time employees who may have access to the personal information of customers, vendors and employees. It is possible such individuals could circumvent the Company'sCompany’s data security controls, which could result in a breach of customer privacy. In addition, third parties may attempt to hack into our systems to obtain data relating to our business plans, products or our proprietary technology. Any failure to maintain or protect these information technology systems and data integrity, including from cyber-attacks, intrusions or other breaches, could result in the unauthorized access to patient data, and personally identifiable information, theft of intellectual property or other misappropriation of assets, or otherwise compromise our confidential or proprietary information and disrupt our operations.

We are subject to the provisions of the U.S. Foreign Corrupt Practices Act and similar foreign anti-corruption laws.

The possessionForeign Corrupt Practices Act (the “FCPA”), as well as similar anti-corruption laws in foreign jurisdictions around the world, generally prohibit companies, their subsidiaries, affiliates, contractors and/or intermediaries, from offering and/or making improper payments, or providing anything of value, to non-U.S. government officials for the purpose of obtaining or retaining business or securing an unfair advantage in business matters.  Certain parts of the world have experienced, or are continuing to experience, some measure of governmental corruption; while in other parts of the world, strict compliance with anti-bribery laws may conflict with local business customs and usepractices.  Both the real estate business and the healthcare business are subject to particular scrutiny in such matters, due to the requirements of personal information in conducting its business subjectnumerous governmental approvals for real estate development and the predominance of government-sponsored healthcare systems around the world.  The Company has established formal policies and procedures that prohibit, and monitor for, conduct which may violate these laws, but we cannot guarantee that employees, affiliates, representatives and/or agents of the Company will not engage in conduct that violates these laws and for which the Company may be held responsible. 

Risks Relating to legislativeOur Real Estate Business

We have initiated an internal investigation into the validity of our subsidiary’s 17.9133% ownership interest in Avalon Jubilee LLC, the owner of property located in Los Lunas, New Mexico. If our investigation ultimately determines that issues exist relating to the validity of our ownership interest in Avalon Jubilee LLC, our financial condition will be materially adversely affected.

On January 12, 2018, we received a copy of a complaint, dated November 17, 2017, that was filed by Alpha Alpha, LLC in the Thirteenth Judicial District Court in the County of Valencia in the State of New Mexico against Avalon Jubilee, LLC, the holding company that owns the property in Los Lunas, New Mexico, HiTex, LLC, MCBB, LLC, Land Strategies, LLC, Ronald R. Cobb and regulatory burdensJohn Does 1 – 5. The suit asks the court to, among other things, determine whether there have been unauthorized transfers of interest in Avalon Jubilee LLC; and declare who are the holders of interests in Avalon Jubilee LLC. Although the complaint does not name our company or any of its subsidiaries or specifically question our interest in Avalon Jubilee LLC, it raises questions about whether the transfers of interest leading to our acquisition of our interest in Avalon Jubilee LLC were properly made in accordance with the Avalon Jubilee operating agreement. We have begun an internal investigation into the validity of our ownership interest in Avalon Jubilee LLC and will disclose the results of that investigation once it has been completed. Accordingly, we may be required to engage in costly litigation to validate our interest in Avalon Jubilee LLC. Alternatively, a court may ultimately determine that we do not own such interest in which our financial condition will be materially adversely affected as we will no longer be the owner of what we believe is a material asset of ours and be left only with potential claims against the transferors of such assets, which may not result in a full recovery of our losses. Either costly litigation or the loss of a material asset and the inability to fully recover such loss through lawsuits against the transferees of our interest in Avalon Jubilee LLC would have a material adverse effect on our financial condition and prospects.

Litigation against us or the Contributor Parties regarding the safeguardingacquisition from the Contributor could result in the payment of damages which could adversely affect our business, financial condition or results of operations.

If any plaintiffs in a litigation against us or the Contributor Parties, or any of their respective directors, secures relief adversely affecting our acquisition under the Contribution Agreement, such relief may result in our company becoming liable for damages related to one or more of the properties acquired from the Contributor. In addition, we could incur significant costs in connection with lawsuits, including costs associated with the indemnification of our directors and officers.


We are entering into a new business line and, therefore, there is only a limited history upon which investors can evaluate our performance and our future business prospects.

We have entered into the Contribution Agreement with the Contributor and the Contributor Parent, pursuant to which the Contributor has contributed real estate assets to our company. This Contribution Agreement represents a new business line for our company, which has no experience in the real estate sector. We will be relying on the experience of our management team for the operation and development of this informationbusiness line. As a result, our business will be subject to the substantial risks which are found in the early stages of a new business venture operating in the competitive real estate industry. Our future growth and development prospects must be evaluated in light of the risks, expenses and difficulties encountered by all companies in such situations, and in particular those companies which operate a business, such as real estate investment, in competitive environments that can be greatly affected by changes in economic conditions.

We may not be able to successfully integrate the acquired real estate business.

A successful integration of the operations of the real estate development business into our company will require that we devote significant management attention and resources to integrating our business practices, operations, and support functions into a public company structure. The challenges we may encounter include preserving customer, supplier, and other important relationships, addressing differences in business cultures, preserving employee morale, and retaining key employees while maintaining focus on meeting our operational and financial goals and the processesreal estate development business, and adequately addressing other business integration issues. The process of integrating a real estate development business, the diversion of management’s attention from other business efforts, and any subsequent delays in the integration process, could adversely affect our business and financial performance and the market price of our stock.

We are subject to demand fluctuations in the real estate industry. Any reduction in demand could adversely affect our business, results of operations, and financial condition.

Demand for properties similar to those owned by us and expected to be followedowned by us is subject to fluctuations that are often due to factors outside our control. We are not able to predict the course of the real estate markets or whether the current favorable trends in those markets can, or will, continue. In the event of an economic downturn, our results of operations may be adversely affected, and we may incur significant inventory impairments and other write-offs, a data breach.major decline in our gross margins from past levels, and substantial losses from operations of this business.

Adverse changes in economic conditions in markets where our real estate investments are or may be made and where prospective purchasers and utilizers of these properties live could reduce the demand for and utilization of these properties and, therefore, adversely affect our operations and financial condition.

The real estate investment business in which we have become involved as a result of our signing of the Contribution Agreement will be conducted in the United States and may also be conducted in various global locales. Adverse changes in economic conditions in these markets, and in the markets where prospective purchasers and utilizers of our to-be-acquired properties live, could negatively impact those properties and their profitability. Unfavorable changes in job growth, employment levels, consumer income and spending patterns, a decline in consumer confidence, increases in interest rates, and an oversupply of similar properties, could reduce the demand, and depress the prices we may ask, for these properties, resulting in lower sales and income from these properties and a negative impact on our results of operations and financial condition.

Adverse weather conditions, natural disasters, and other unforeseen and/or unplanned conditions could disrupt our real estate developments.

Adverse weather conditions and natural disasters, such as hurricanes, tornadoes, earthquakes, floods, droughts, and fires, could have serious impacts on our ability to develop and market individual real estate offerings. Properties that we look to acquire may also be affected by unforeseen planning, engineering, environmental, or geological conditions or problems, including conditions or problems which arise on third party properties adjacent to or in the vicinity of properties which we expect to own and which may result in unfavorable impacts on our prospective properties. As our proposed real estate investments may be located in multiple countries, with differing climates and geological characteristics, each property will face different known and unknown risks. Any interferenceadverse event or circumstance could cause a delay in, prevent the completion of, or increase the cost of, one or more of these properties expected to be developed and brought to market by us, thereby resulting in a negative impact on our operations and financial results.


If the market value of our real estate investments decreases, our results of operations will also likely decrease.

The market value of each real estate investment will depend on market conditions both locally and globally. We expect to acquire land for each expansion into a new market at a cost based upon then-current economic conditions. If local and/or global economic conditions deteriorate, or if the demand for such properties decreases below the levels anticipated at the time of acquisition of a property, we may not be able to make a profit on such property comparable to those profits made by the Contributor and the Contributor Parent in the past. As a result of declining economic conditions, we may experience lower than anticipated or forecast results or profits, and/or may not be able to recover our costs of a project when a property is brought to market.

We rely on subcontractors to construct each property, and on building supply companies to provide components for each property’s construction. The failure of one or more of these subcontractors to properly construct these facilities, or any defects in the components obtained from building supply companies, could adversely affect these properties, and thus our operations.

We engage and rely on subcontractors to perform the actual construction of the buildings upon each property we purchase. Also, we purchase the components used in our construction projects from third party independent building supply companies. We utilize industry standard quality control programs, but despite these programs, we may find that subcontractors are utilizing improper construction practices or the components purchased from building supply companies do not perform as specified in the project’s plans. We may also find that our subcontractors are inadequately capitalized or have insufficient staffing to undertake the required work. In such events, we may incur substantial additional costs to repair substandard construction at our properties, to comply with the plans and local legal requirements. The cost of satisfying local legal building code obligations may be significant, and we may not be able to recover these costs from our subcontractors, suppliers and/or unauthorizedtheir respective insurers.

Legal challenges or governmental regulations may delay the start or completion of construction on our projected real estate ventures, increase our expenses, or limit our construction activities, which could have a negative impact on operations.

Each of our current and future real estate developments may experience a delay and/or increased expenses in construction, marketing and/or operation due to legal challenges to the development. These challenges may be brought by private parties or by governmental authorities, resulting in delays in the start or completion of each project’s construction or requiring changes to the design or construction of each development. Any delay or change in a development’s construction would result in increased expenses to us in the development of the property, which could in turn negatively impact our financial results with respect to that development and with respect to our overall operations.

Numerous governmental authorities are typically involved in each new development project, and such authorities have broad discretion in exercising their approval authority. Various local, state, and federal statutes, ordinances, rules, and regulations concerning building, zoning, sales, and similar matters apply to and/or affect the real estate development industry and govern matters including construction, marketing, sales, operation, lending, and other activities concerning each development. In the United States, there have been numerous changes in regulations that limit the availability or use of land, including regulations which limit growth in certain communities, the use of utilities including water and sewer outlets, road construction and utilization, and other related matters. Each jurisdiction in which we expect to invest in real estate development will have different and varying levels of regulation which must be taken into account when planning and implementing such developments. For example, we may be required to change or modify our plans due to alterations in local planning or laws. As a result, we could incur substantial costs related to compliance with legal and regulatory requirements with regard to each real estate development, negatively impacting our business by causing delays, increasing costs, or limiting our ability to operate in those locations.


If a development project experiences increased costs or shortages of labor or components, or other circumstances beyond our control, there could be delays or increased costs in developing such project, which could negatively impact our finances and operating results.

We may invest in real estate development projects in a number of countries and regions, including the United States Each project may be negatively impacted by local circumstances beyond our control, including labor shortages, disputes and work stoppages, union organizing activities, price changes and delays in availability of building materials and components, and a lack of adequate utility and road infrastructure and services. Any change in these circumstances could delay the start or completion of, or increase the cost of, one or more developments. We may not be able to recover any additional such costs through an increase in the prices for our properties, and therefore our operating results may be negatively affected.

Changes in tax laws, taxes or fees may increase the cost of each development, and such changes could adversely impact our finances and operational results.

Each development project will be subject to different tax laws, tax levies and governmental fees, depending upon its geographic location. Any increase or change in such laws, taxes, or fees, including real estate property taxes, and fees to fund schools, open space, utility and road improvements, could increase the cost of a development and thus have an adverse effect on our operations. Such changes could also negatively impact potential and/or actual users and purchasers of a development because potential buyers may factor such changes into their decisions to utilize or purchase a property.

We will incur significant advance costs in each real estate development before that development begins to generate revenue from sales and/or public usage, and as a result, we may not recover our costs in whole or in part, may recover those costs slower than originally anticipated, or may incur higher costs as a result of any delays in completion of a project, resulting in an adverse impact to our operating results.

We expect to make a number of significant cash outlays for each real estate development before the construction on that development begins, and considerably before any development begins to generate revenue. Such cash outlays will include expenditures to buy, rent, lease or otherwise acquire land, to plan, design and develop a property, to conduct site studies as necessary for development, to provide basic utility and infrastructure access to this informationa property, to obtain permits, licenses, and other required regulatory approvals, to post surety bonds and such other construction guarantees as required by law, and to actually construct the project building(s) and to fully develop a property. These processes can take up to several years before a development is completed and ready to generate any revenue for us. The time to complete each development will vary, based on local geographic conditions, legal requirements, regulatory and community concerns, the ability to obtain required construction materials and labor, and other factors that may be unique to each project. We will face the risk that, during construction, demand for a project may change, alter or decline, and we may be forced to take steps to adjust to these changes in demand, including altering a project and its scope, and selling the property at lower than anticipated or planned prices or at prices that generate lower profit margins or losses. Inflation, economic changes or downturns, asset carrying costs (including interest on funds that are used to acquire land and/or construct a building) may also be generated and may be significant. As a result of these factors, we may experience adverse impacts on our operating results, and if a development experiences a significant decline in value, we may also be required to recognize material write-downs of the book value of a project building in accordance with GAAP.

The real estate industry is highly competitive and if other property developers are more successful or offer better value to customers, our business could suffer.

The real estate industry is highly competitive, regardless of locale, and we will face competitors in each location where we develop, construct, market, sell and/or operate real estate ventures. Competitors will range from small local companies to large international conglomerates with financial resources much greater than those of our company. We have to compete in each market for land, raw materials, construction components, financing, environmental resources, utilities, infrastructure, labor, skilled management, governmental permits and licensing and other factors critical to the successful development of each project. We compete against both new and existing developments and developers. Any increase in or change to any competitive factor could result in our inability to begin or complete development of a project in a timely manner, increased costs for the design, development and completion of a project, and/or higher costs and/or lower revenues from the marketing, sales and/or operation of a development. As a result, we may experience lower revenue and decreased profits due to these factors, impacting our operations and our overall financial results.

Future terrorist activity and/or international instability could adverse impact our real estate developments and financial operations.

We expect to operate real estate developments in a variety of locales, including the United States. A terrorist attack against the United States or other foreign country, an increase in terroristic threats or suspected activity, and/or an increase in domestic or international instability, whether or not located in a country in which we have real estate assets, could significantly affect our business by slowing, delaying or halting construction of real estate developments, increasing the cost of such developments, and/or reducing the sales and/or usages of such properties, thereby adversely affect our business.


We may incur environmental liabilities with respect to our development projects.

The properties we will target for investment will be subject to a variety of local, state and federal statutes, ordinances, rules and regulations concerning the protection of health and the environment. The particular environmental laws that apply to any given community vary greatly according to the community site, the site’s environmental conditions and the present and former use of the site. Environmental laws may result in delays, may cause us to lose existing customers; have difficulty preventing, detecting, and controlling fraud; cause disputes with customers, physicians,incur substantial compliance and other health care professionals; render uscosts and may prohibit or severely restrict development in certain environmentally sensitive regions or areas. Furthermore, under various federal, state and local laws, ordinances and regulations, an owner of real property may be liable for the costs or removal or remediation of certain hazardous or toxic substances on or in such property. Such laws often impose such liability without regard to whether we knew of, or were responsible for, the presence of such hazardous or toxic substances. The cost of any required remediation and our liability therefor as to any property are generally not limited under such laws and could exceed the value of the property and/or the aggregate assets of our company. The presence of such substances, or the failure to properly remediate contamination from such substances, may adversely affect our ability to sell the real estate or to borrow using such property as collateral.

If we fail to diversify our real estate investment portfolio, downturns relating to certain geographic regions, types of assets, industries or business sectors may have a more significant adverse impact on our income and assets than if we had a diversified development property portfolio.

We are not required to observe specific diversification criteria. Therefore, our target portfolio may at times be concentrated in certain asset types that are subject to legal claimshigher risk of foreclosure or secured by assets concentrated in a limited number of geographic locations. To the extent that our real estate portfolio will be concentrated in limited geographic regions, types of assets, industries or business sectors, downturns relating generally to such region, type of asset, industry or business sector may result, for example, in tenants defaulting on their lease obligations at a number of properties within a short time period, which may reduce future projected net income and liability;the value of our publicly traded securities and, accordingly, adversely affect our business and prospects.

Our co-venture partners, co-tenants or other partners in co-ownership arrangements could take actions that decrease the value of an investment to us and lower our valuation.

Certain of the development properties could involve joint ventures, tenant-in-common investments or other co-ownership arrangements with third parties having investment objectives that are may or may not be similar to those of our company for the acquisition, development or improvement of properties, as well as the acquisition of real estate-related investments. We also may purchase and develop properties in joint ventures or in partnerships, co-tenancies or other co-ownership arrangements with the sellers of the properties, affiliates of the sellers, developers or other persons. Such investments may involve risks not otherwise present with other forms of real estate investment, including, for example:

the possibility that a co-venturer, co-tenant or partner in an investment might become bankrupt;

the possibility that the investment may require additional capital that we or our partner do not have, which lack of capital could affect the performance of the investment or dilute our interest if the partner were to contribute our share of the capital;

the possibility that a co-venturer, co-tenant or partner in an investment might breach a loan agreement or other agreement or otherwise, by action or inaction, act in a way detrimental to us or the investment;

that such co-venturer, co-tenant or partner may at any time have economic or business interests or goals that are or that become inconsistent with the business interests or goals of our company;

the possibility that we may incur liabilities as the result of the action taken by our partner or co-investor;

that such co-venturer, co-tenant or partner may be in a position to take action contrary to our instructions or requests or contrary to our policies or objectives; or


that such partner may exercise buy/sell rights that force us to either acquire the entire investment, or dispose of our share, at a time and price that may not be consistent with our investment objectives.

Any of the above might subject a property to liabilities in excess of those contemplated and thus reduce our returns on that investment.

Uninsured losses relating to real property or excessively expensive premiums for insurance coverage may adversely affect the value of your stock.

The nature of the activities at certain properties could expose us and our operators to potential liability for personal injuries and, in certain instances, property damage claims. For instance, there are types of losses, generally catastrophic in nature, such as losses due to wars, acts of terrorism, earthquakes, pollution, environmental matters or extreme weather conditions such as hurricanes, floods and snow storms that are uninsurable or not economically insurable, or may be insured subject to limitations, such as large deductibles or co-payments. We may not carry all the usual and customary insurance policies which would be carried by a similarly-positioned company, and we may not be carrying those insurance policies in amounts and types sufficient to cover every risk which may be encountered by our company. Insurance risks associated with potential terrorist acts could sharply increase the premiums we will pay for coverage against property and casualty claims. Mortgage lenders generally insist that specific coverage against terrorism be purchased by commercial property owners as a condition for providing mortgage, bridge or mezzanine loans. It is uncertain whether such insurance policies will be available, or available at reasonable cost, which could inhibit our ability to finance or refinance our planned to-be-acquired properties. In such instances, we may be required to provide other financial support, either through financial assurances or self-insurance, to cover potential losses. We cannot assure you that it will have adequate coverage for such losses. If any of our properties incur a casualty loss that is not fully covered by insurance, the value of our assets will be reduced by the amount of any such uninsured loss. In addition, other than the capital reserve or other reserves we may establish, we do not expect to have any contingent sources of funding in place to repair or reconstruct any uninsured damaged property, and we cannot assure you that any such sources of funding will be available to us for such purposes in the future. Also, to the extent we must pay unexpectedly large amounts for insurance, we could suffer reduced earnings that would result in regulatory sanctionsa decreased value attributed to our publicly traded stock.

We could face losses with respect to abandoned predevelopment costs.

The development process inherently requires that a large number of opportunities be pursued with only a few being developed and constructed. We may incur significant costs for predevelopment activity for projects that are abandoned that directly affect our results of operations. We expect to institute procedures and controls that are intended to minimize this risk, but it is likely that there will be predevelopment costs charged to expense on an ongoing basis.

We may not have adequate financing to fund our future property acquisitions and project developments, and such capital resources may not be available to us on commercially reasonable terms, or penalties;at all.

The implementation of our new business plan including the prospective acquisition of development properties and the completion of construction projects on such properties will involve considerable sums of capital. We currently do not have any such capital and will be required to raise acquisition, construction and related funds in the future on a project by project basis. We may not be successful in our efforts to raise such funds, or capital that we can acquire may not be reasonably priced. In such a case, we may not be able to successfully effect our new business plan. Such a failure would have a material adverse effect on our financial results, our future business prospects and our public market stock valuation.

Risk Factors Relating to Legacy LHE Business

We are exposed to credit risk of some of our customers.

We accept payment for certain of our products through credit cards and customer financing and our exposure to these credit risks may increase during an economic slowdown. Although we have programs in place that are designed to monitor and mitigate the associated risk, there can be no assurance that such programs will be effective in reducing our credit risks. Future losses, if incurred, could harm our business and have an effect on our operating results and financial condition.


We may be adversely affected by product liability claims, unfavorable court decisions or legal settlements.

Sales of the LHE products may lead to potential product liability claims arising from the design, manufacture and marketing of these products. Such claims may be subject to many uncertainties and outcomes which are not predictable, and we may incur significant legal expenses and causein defending these claims regardless of whether we are found to be liable for the claims. While we carry certain product liability insurance coverages, the actual cost to us to incur additional significant expenses or lose revenues; render us unable to accept and process credit card transactions in our consumer businesses; or suffer other adverse consequences,of any product liability claim could be materially different than the amount of the current coverages we carry, which could have a material adverse effect on our business, financial condition or results of operations.

If the Company fails to manage its and its subsidiaries' growth effectively, its businesses could be disrupted which could harm its operating results.
The Company has experienced, and may in the future experience, growth in its business, both organically and through the acquisition of businesses and product lines. The Company expects to make significant investments to enable its future growth through, among other things, new product innovation and clinical trials for new applications and products.
In addition, if private carriers continue to approve favorable reimbursement policies for psoriasis and the Company's marketing programs are successful in increasing utilization of its XTRAC system, the Company expects to experience growth in the number of its employees and customers and the scope of its operations.
Such growth may place a strain on the Company's management and operations. The Company's ability to manage this growth will depend upon, among other factors, its ability to broaden its management team; its ability to attract, hire, train, motivate and retain skilled employees; and the ability of its officers and key employees to continue to implement and improve its operational, financial and other systems, to manage multiple, concurrent customer relationships and different products and to respond to increasing compliance requirements. The Company's future success is heavily dependent upon achieving such growth and acceptance of its products. Any failure to effectively manage future growth could have a material adverse effect on the Company's business,position, results of operations and financial condition.
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The Company is exposed to risks associated with credit card and payment fraud and with credit card processing, which could cause the Company to lose revenue.
A significant part of the payments for its products and services are processed by the Company through credit cards or automated payment systems. The Company has suffered losses, and may continue to suffer losses, as a result of orders placed with fraudulent credit cards or other fraudulent payment data. For example, under current credit card practices, the Company may be liable for fraudulent credit card transactions if it does not obtain a cardholder's signature, a frequent and accepted practice in internet sales. In addition, charges under these payment methods may be challenged as fraudulent or unauthorized for a significant period of time after the purchase of the goods and services, often up to 18 months after the transactions. While the Company employs technology solutions to help it detect fraudulent transactions, those solutions are not guaranteed to uncover all fraudulent transactions. Therefore, the failure to detect or control payment fraud could cause the Company to lose sales and revenue and incur additional costs in managing fraud-control processes.
Any significant interruptions in the operations of its third-party call centers could cause the Company to lose sales and disrupt its ability to process orders and deliver its solutions in a timely manner.
The Company relies on third-party call centers to sell its products, respond to customer service and technical support requests and process orders. Any significant interruption in the operation of these facilities, including an interruption caused by its failure to successfully expand or upgrade its systems or to manage these expansions or upgrades, could reduce its ability to receive and process orders and provide products and services, which could result in lost and cancelled sales and damagecash flows.

Risks Relating to the Company's brand and reputation.

AsMarket for Our Common Stock Generally

Notice of Delisting or Failure to Satisfy a Continued Listing Rule or Standard

On February 20, 2018, we received written notification from The Nasdaq Stock Market that the Company grows, it will need more capacity from those existing call centers, orclosing bid price of our common stock had been below the Company will need to identify and contract with new call centers. The Company may not be able to continue to locate and contract for call center capacity on favorable terms, or at all. Additionally, the rates those call centers charge the Company may increase, or those call centers may not continue to provide service at the current levels.

If the Company's third-party call center operators do not convert inquiries into sales at expected rates, its ability to generate revenue could be impaired. Training and retaining qualified call center operators is challenging, and if the Company does not adequately train its third party call center operators, they will not convert inquiries into sales at an acceptable rate.
The Company is reliant on a limited number of suppliers for production of key products.
Production of the Company's XTRAC system requires specific component parts obtained from the Company's suppliers. Production of the Company's surgical laser systems requires some component parts that may become harder to procure as the design of a system ages. Similarly, the Company's skincare products may require compounds that can be efficiently produced only by a limited number of suppliers. The Company has one primary supplier of LEDs for its PTL business and relies on contract manufacturers. While the Company believes that it could find alternate suppliers, in the event that its suppliers fail to meet its needs, a change in suppliers or any significant delay in the Company's ability to have access to such resources could have a material adverse effect on its delivery schedules, business, operating results and financial condition. Moreover, in the event the Company can no longer utilize this supplier or acquire this resource and must identify a new supplier or substitute a different resource, such change may trigger an obligationminimum $1.00 per share for the Company to comply with additional FDA regulatory requirements including, but not limited to, pre-marketing authorization and QSR requirements.
Finally, the Company's no!no! brand products are sourced from one main supplier. The Company believes there are other, potential sources for the manufacture of these products. However, should our main supplier be unable to meet our production demands or cease doingprevious 30 consecutive business we may encounter difficulty in transitioning our products to another manufacturer,days, and that other manufacturer or manufacturers may not be able to meet our production requirements. Any change in supplier or any significant delay in transition to a new supplier may have a material adverse effect on the delivery schedules for these products, our ability to meet customer demand, business, operating results and financial condition.
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The Company's failure to respond to rapid changes in technology and its applications in the medical devices industry or the development of a cure for skin conditions treated by its products could make its treatment system obsolete.
The medical device industry is subject to rapid and substantial technological development and product innovations. To be successful, the Company must respond to new developments in technology, new applications of existing technology and new treatment methods. The Company may also encounter greater pressure for innovation in order to satisfy a demand for novelty in the consumer market. The Company's financial condition and operating results could be adversely affected if the Company fails to be responsive on a timely and effective basis to competitors' new devices, applications, treatments or price strategies. For example, the development of a cure for psoriasis, vitiligo, atopic dermatitis or leukoderma would eliminate the need for the Company's XTRAC system for these diseases and would require the Company to focus on other uses of its technology, which would have a material adverse effect on its business and prospects.
As the Company develops new products or improves its existing products, the Company may accelerate the economic obsolescence of the existing, unimproved products and their components. The obsolete products and related components may have little to no resale value, leading to an increase in the reserves the Company has against its inventory. Likewise, there is a risk that the new products or improved existing products may not achieve market acceptance and therefore may also lead to an increase in the reserves against the Company's inventory.
The Company's marketing campaigns and advertising may be attacked as false and misleading, and our media spending might not result in increased net sales or generate the levels of product and brand name awareness that the Company desires. The Company might not be able to increase its net sales at the same rate as it increases its advertising and marketing expenditures.
The Company's future growth and profitability will depend in part on the effectiveness and efficiency of its marketing campaigns and media spending, including its ability to:
create greater awareness of its products and brand name;
determine the appropriate creative message and media mix for future expenditures; and
effectively manage advertising costs, including creative and media costs, to maintain acceptable costs in relation to sales levels and operating margins.
The Company's no!no!® Hair and other consumer product's portfolio of infomercials advertising, and other forms of media may not result in increased sales or generate desired levels of product and brand name awareness, and may be attacked as false and misleading. The Company may not be able to increase its net sales at the same rate as it increases its advertising expenditures or may be required to defend against inaccurate claims of false advertising. The Company is currently the subject of certain legal proceedings relating to its advertising claims in the U.S. The Company has voluntarily made changes to its advertising as part of its usual process for reviewing and updating its advertising through the various media and sales channels we rely upon, and which address certain of the claims made in these matters. These changes have not adversely affected the Company's sales of the no!no!® Hair products in the U.S. to date; however the Company may be required to make other changes in the future in response to existing or potential legal proceedings that could materially and adversely affect such sales.
The Company periodically updates the content of its infomercials and revises its product offerings. If customers are not as receptive to new infomercial content or product offerings, the Company's sales through its infomercial sales channel will decline. In addition, if there is a marked increase in the price that the Company pays for its media time, or a marked decrease in the availability of media time to be purchased by the Company, the cost-effectiveness of its infomercials will decrease. If the Company's infomercials are broadcast during times when viewership is low, this could also result in a decrease of the cost-effectiveness of such broadcasts, which could cause its results of operations to suffer. Also, to the extent the Company has committed in advance for broadcast time for its infomercials, the Company would have fewer resources available for potentially more effective distribution channels.
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A higher than anticipated level of product returns may adversely affect the Company's business and its customers, or physicians and technicians, as the case may be, may misuse certain of its products, and product and other damages imposed on the Company may exceed its insurance coverage, or the Company may be subject to claims that are not covered by insurance.
The Company offers consumers who purchase its consumer products, including its no!no!® brands directly from the Company a money-back guarantee, subject to time and certain other limitations. Retailers and home shopping channels are also permitted to return the consumer products, subject to certain limitations. The Company establishes revenue reserves for product returns based on historical experience, estimated channel inventory levels and other factors. If product returns exceed estimates, the excess would offset reported revenue, which could negatively affect the Company's financial results. Product returns and the potential need to remedy defects or provide replacement products or parts for items shipped in volume could result in substantial costs, the requirement to conduct an FDA recall and/or submit an FDA-required report of a correction/removal and have a material adverse effect on the Company's business and results of operations.
The Company may be subject to product liability claims from time to time. A number of the Company's products are highly complex and some are used to treat delicate skin conditions on and near a patient's face. In addition, the clinical testing, manufacturing, marketing and use of certain of the Company's products and procedures may also expose the Company to product liability, FDA regulatory and/or legal actions, or other claims. Certain indications for use for the Company's PTL light-based devices, though approved outside the U.S., are not approved in the U.S. If a physician elects to apply an off-label use and the use leads to injury, the Company may be involved in costly litigation. In addition, the fact that the Company trains technicians whom it does not supervise in the use of its XTRAC system during patient treatment may expose the Company to third-party claims if those doing the training are accused of providing inadequate training. The Company presently maintains liability insurance with coverage limits of at least $10,000,000 per occurrence and overall aggregate, which the Company believes is an adequate level of product liability insurance, but product liability insurance is expensive and the Company might not be able to obtain product liability insurance in the future on acceptable terms or in sufficient amounts to protect the Company, if at all. A successful claim brought against the Company in excess of its insurance coverage could have a material adverse effect on its business, results of operations and financial condition. In addition, continuing insurance coverage may also not be available at an acceptable cost, if at all. Therefore, the Company may not be able to obtain insurance coverage that will be adequate to satisfy a liability that may arise. Regardless of merit or eventual outcome, product liability claims may result in decreased demand for a product, injury to its reputation, withdrawal of clinical trial volunteers and loss of revenues. As a result, regardless of whether the Company is insured, a product liability claim or product recall may result in losses that could result in the FDA taking legal or regulatory enforcement action against the Company and or its products including recall, and could have a material adverse effect upon the Company's business, financial condition and results of operations.
The Company's costs could substantially increase if it experiences a significant number of warranty claims.
The Company provides 12-month embedded product warranties, and offers longer warranties available for separate purchase, against technical defects of its no!no!® line of hair removal products and other consumer products. Its product warranty requires the Company to repair defective parts of its products, and if necessary, replace defective components. Historically, the Company has received a limited number of warranty claims for these products. The costs associated with such warranty claims have historically been relatively low. Thus, the Company generally does not accrue a significant liability contingency for potential warranty claims.
If the Company experiences an increase in warranty claims, or if its repair and replacement costs associated with such warranty claims increase significantly, we will begin to incur liabilities for potential warranty claims after the sale of its products at levels that the Company has not previously incurred or anticipated. In addition, an increase in the frequency of our warranty claims or amount of warranty costs may harm our reputation and could have a material adverse effect on its financial condition and results of operations.
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The Company may be subject to litigation that will be costly to defend or pursue and uncertain in its outcome.
The Company's business may bring it into conflict with its licensees, licensors, or others with whom the Company have contractual or other business relationships, or with its competitors or others whose interests differ from it. If the Company is unable to resolve those conflicts on terms that are satisfactory to all parties, the Company may become involved in arbitration and/or litigation brought by or against it. Such actions are likely to be expensive and may require a significant amount of management's time and attention, at the expense of other aspects of our business. The outcome of arbitration or litigation is always uncertain, and in some cases could include judgments against the Company that require it to pay damages, enjoin it from certain activities, or otherwise affect its legal or contractual rights, which could have a significant adverse effect on its business. In addition, while the Company maintains insurance for certain risks, the amount of its insurance coverage may not be adequate to cover the total amount of all insured claims and liabilities. It also is not possible to obtain insurance against all potential risks and liabilities. The Company cannot predict what the outcome will be in any ongoing or threatened arbitrations and/or litigations, and any adverse results in any such actions may also materially and negatively impact its business, the market price of its common stock, cash flow, prospects, revenues, profitability or capital expenditures, or have other material adverse effects on its business, reputation, results of operations, financial condition or liquidity.
From time to time, the Company may be threatened with material litigation.
From time to time, the Company is threatened with individual and class action litigations involving its business, products, advertisements, packaging, labeling, consumer claims, contracts, agreements, intellectual property, SEC or FDA matters, licenses and other areas involving it and its business. The outcome or effect on its business, the market price of the Company's common stock, cash flows, prospects, revenues, profitability, capital expenditures, reputation, demand for its products, results of operations, financial condition or liquidity of any future litigation cannot be predicted by the Company. Except as disclosed in Item. 3, Legal Proceedings, no such current pending matters, if any, are believed to be significant.
Litigation is inherently unpredictable and may:
result in rulings that are materially unfavorable to the Company, including claims for significant damages, fines or penalties, and administrative remedies, or other rulings that prevent it from operating its business in a certain manner;
cause the Company to change its business operations to avoid perceived risks associated with such litigation; and
require the expenditure of significant time and resources, which may divert the attention of management and interfere with the pursuit of the Company's strategic objectives.
While the Company maintains insurance for certain risks, the amount of its insurance coverage may not be adequate to cover the total amount of all insured claims and liabilities. It also is not possible to obtain insurance against all potential risks and liabilities. If any litigation were to have a material adverse result, there could be a material impact on the Company's results of operations, cash flows or financial position.
The Company depends on its executive officers and key personnel to implement its business strategy and could be harmed by the loss of their services and the inability to attract personnel for these positions.
The Company believes that its growth and future success will depend in large part upon the skills of its key management, technical and scientific personnel. Certain members of the Company's management staff as well as other key employees may voluntarily terminate their employment with the Company at any time, with or without notice. There is substantial competition for personnel in the industries in which we operate, and we may face increased competition for such employees, resulting in the need to compensate these personnel at a higher-than-anticipated rate, a delay in replacing such personnel and integrating them into the Company's operations, and the possibility that we may be unable to attract and retain these personnel. The loss of the services of key personnel, or the inability to attract and retain additional qualified personnel, could result in delays to product development or approval, loss of sales and diversion of management resources, and may have an adverse effect on our business and our ability to grow that business.
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In particular, the Company's success depends in part upon the continued service and performance of Dr. Dolev Rafaeli and Dennis M. McGrath. The Company has fixed-term employment agreements with Dr. Rafaeli and Mr. McGrath; however, there are no assurances that the services of these individuals will be available to the Company for any specified period of time. The loss of the services of one or both of these officers could adversely affect the Company's ability to develop and introduce its new products.
Additionally, the Company does not currently maintain "key person" life insurance on the lives of Dr. Rafaeli, Mr. McGrath, its other executives or any of its employees. The Company's lack of insurance means that it may not have adequate compensation for the loss of the services of its key employees, which could affect the Company's ability to maintain the level of services formerly provided by those persons.
In our industry, there is substantial competition for key personnel in the regions in which we operate and we may face increased competition for such employees, particularly in emerging markets as the trend toward globalization continues. If we are unable to attract key personnel in a timely manner, including key sales and other personnel who have critical industry experience and relationships in the regions in which we operate, including in emerging markets, it may have an adverse effect on our business and our ability to drive growth, including through execution of our strategic initiatives. Furthermore, some of the key personnel for whom we compete have post-employment arrangements with their current or former employer that may impact our ability to hire them or expose us and them to claims. In addition, if we are unable to retain and focus our existing key personnel it may have an adverse effect on our business, financial condition and results from operations. Changes in our senior management structure could lead to inefficiencies in our ability to execute our strategic, cost-reduction and efficiency initiatives, which may have an adverse effect on our business and results of operations.
It may be difficult for any of the Company's stockholders to effect service of process and enforce their rights against the Company or its officers and directors in foreign courts.
Certain of the Company's operating subsidiaries' assets are located outside the United States, including locations in Israel, the United Kingdom, Brazil, Korea, Hong Kong, Columbia and India. As a result, the Company's stockholders may find it difficult to enforce their legal rights in the courts of these countries based on the civil liability provisions of the United States federal securities laws as applied in the courts of the United States or these countries, even if civil judgments are obtained in courts of the United States. In addition, it is unclear if extradition treaties in effect between the United States and these countries would permit effective enforcement against any of the Company's officers and directors that reside outside the United States of criminal penalties, whether sought under the United States federal securities laws or other applicable laws.
Currency exchange rate fluctuations could adversely affect the Company's operating results.
Some of the Company's operating expenses are denominated in New Israeli Shekel ("NIS"). Any significant fluctuation in the value of the NIS may materially and adversely affect its cash flows, earnings and financial position. For example, an appreciation of NIS against the U.S. dollar would make any new NIS denominated investments or expenditures more costly to the Company, to the extent that it needs to convert U.S. dollars into NIS for such purposes. Furthermore, because certain parts of our business include international business transactions, costs and prices of its products or components in overseas countries, such transactions are affected by foreign exchange rate changes.
The majority of sales invoicing for the Company's PTL business is done in Pounds Sterling, Euros or U.S. dollars, while product costs and the overhead of the offices in the United Kingdom are denominated in Pounds Sterling. The sales invoicing for the LK Technology business is done in Brazilian Real. The Company's U.S. operations, with U.S. dollar operating costs, serve to reduce the exposure to fluctuations in the value of the Pound Sterling, the Euro, or the Brazilian Real. To the extent that the Company adjusts its invoicing practices for its PTL and LK Technology businesses, or if the remainder of its business (or any portion thereof) ceases to be conducted primarily in U.S. dollars, the Company's exposure to the market's currency conditions could present a greater risk to it.
As a result, foreign exchange rate fluctuations may adversely affect the Company's business, operating results and financial condition.
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The Company's ability to use its net operating loss carryforwards to offset future taxable income for U.S. federal income and U.K. business tax purposes may be limited as a result of "ownership changes" of PhotoMedex caused by the merger. In addition, the amount of such NOL carryforwards could be subject to adjustment in the event of an IRS examination.
If a corporation undergoes an "ownership change" under Section 382 of the U.S. Internal Revenue Code, the amount of its pre-change net operating losses, which we refer to in this report as "NOLs", that may be utilized to offset future taxable income is subject to an annual limitation. In general, an ownership change occurs if the aggregate stock ownership of certain stockholders increases by more than 50 percentage points over such stockholders' lowest percentage ownership during the applicable testing period (generally three years).
The annual limitation generally is determined by multiplying the value of the corporation's stock immediately before the ownership change by the applicable long-term tax-exempt rate. Any unused annual limitation may, subject to certain limits, be carried over to later years, and the limitation may under certain circumstances be increased by recognized built-in gains or reduced by recognized built-in losses in the assets held by the corporation at the time of the ownership change. Similar rules and limitations may apply for state income tax purposes.
The reverse merger, effected on December 13, 2011, did result in an ownership change of PhotoMedex. The Company estimated that it would have approximately $56.8 million of U.S. net operating loss carryforwards that can be utilized through the annual limitations and also through the realization of its built-in gains through amortization in the first 5 years following December 13, 2011. The balance of the net operating loss carryforwards of pre-merged PhotoMedex amounts was estimated to be approximately $53.5 million. This balance could only be utilized through realization of the built-in gains other than by means of amortization. On December 27, 2012, PhotoMedex made an internal realignment of its operations by selling its operating businesses to a wholly-owned, non-consolidated U.S. subsidiary, and thereby realized sufficient gain to offset approximately $45 million of such balances of the $53.5 million of net operating losses.
In addition, the amount of the NOL carryforwards is subject to review and audit by the Internal Revenue Service (the "IRS"). There can therefore be no assurance that the benefit of such NOL carryforwards will be fully realized.
Likewise, if a corporation undergoes an "ownership change" and/or a "change in trade or business" under various standards of Her Majesty's Revenue and Customs (HMRC, U.K.), the amount of a company's pre-change NOLs that may be utilized to offset future taxable income in the U.K. may be limited or not available for offset against that income. After evaluating the effects of the reverse merger and integration of Radiancy's business on its U.K. NOLs; management determined that the NOLs remain usable against future income of the UK subsidiary. However, the amount of the NOL carryforwards remains subject to review and audit by the HMRC. There can therefore be no assurance that the benefit of such NOL carryforwards will be fully realized.
Risks Related to the Company's Intellectual Property Matters
If the Company is unable to adequately protect or enforce its rights to intellectual property or secure patents right to technologies that it develops, the Company may, experience reduced market share, assuming any, or incur costly litigation to enforce, maintain or protect such rights.
The Company's success depends in part on its ability to maintain and defend patent protection for its products, to preserve its trade secrets and to operate without infringing the proprietary rights of third parties. However, the Company cannot guarantee that the patents covering certain of its technologies and processes will not be contested, found to be invalid, unenforceable or owned by another or circumventable. There can be no assurance that its pending patent applications will result in patents being issued, or that its competitors will not circumvent, or challenge the validity of, any patents issued to the Company. Any such objections and rejections may adversely affect the Company's other patents and patent applications.  There can be no assurance that measures taken by the Company to protect its proprietary information will prevent the unauthorized disclosure or use of this information or that others will not be able to independently develop such information. In addition, in the event that another party infringes its patent rights or other proprietary rights, the enforcement of such rights can be a lengthy and costly

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process, with no guarantee of success. Moreover, there can be no assurance that claims alleging infringement by the Company of the proprietary rights of others will not be brought against the Company in the future or that any such claims will not be successful. If the Company is unable to maintain the proprietary nature of its technologies, its ability to market or be competitive with respect to some or all of its products may be affected, which could reduce its sales and affect its profitability. Also, as the Company's patents expire, competitors may utilize the technology found in such patents to commercialize their own products. Moreover, while the Company seeks to secure additional patents on commercially desirable improvements, there can be no assurance that the Company will be successful in securing such patents, or that such additional patents will adequately offset the effect of expiring patents. Further, pending patent applications are not enforceable.
The Company's policy is to file patent applications and to protect certain technology, inventions and improvements that are commercially important to the development of the Company's business. The Company's strategy has been to apply for and maintain patent protection for inventions and their applications which it believes has potential commercial value in countries that offer significant market potential. Because of the high costs of applying for, procuring and maintaining patents, the Company is unable to file patent applications covering all of its products in every country and as a result its patents are limited in scope and geographic coverage and may not protect the Company from competing products in those markets.
The Company will rely on certain of its PTL patents to protect the home-use market for two of its PTL hand-held devices. If the patents prove unenforceable or circumventable, the Company may not attain growth and may lose market share from these PTL products.
The Company's success may depend, in part, on its ability to continue to use certain software in its products and in its business. This software may have been created by contractors to the Company or may include third-party software such as open source software. There is a possibility that claims will be made that this software infringes the copyright and/or trade secret rights of one or more third parties and that such claims may affect the Company's right to use the software.
From an international perspective, protection of intellectual property outside of the U.S. is uncertain to the Company. The laws of some countries may not protect the Company's intellectual property rights to the same extent as laws in the U.S. The intellectual property rights the Company enjoys in one country or jurisdiction may be rejected in other countries or jurisdictions, or, if recognized there, the rights may be significantly diluted. This may affect the Company's ability to commercialize its products, grow its product sales and maintain market share in countries outside the U.S. It may be necessary or useful for the Company to participate in proceedings to determine the validity of its foreign intellectual property rights, or those of its competitors, which could result in substantial cost and divert its resources, efforts and attention from other aspects of its business.
The Company's trademarks are limited in scope and geographic coverage and may not significantly distinguish the Company from its competition. The Company's trade secrets are also limited in scope and geographic coverage and may not adequately protect the Company from products offered by our competitors.
The Company owns several key federal and international trademark registrations and has federal trademark applications pending in the United States and abroad for additional trademarks. Even if those federal registrations are granted to the Company, its trademark rights may be challenged. Further, as registration is usually a requirement for protection in most foreign countries, if the Company has not registered its marks, it may not have any enforceable rights. It is also possible that its competitors will adopt trademarks similar to the Company's, thus impeding its ability to build brand identity and possibly leading to customer confusion. Third parties could register trademarks that are similar to the Company's in the United States and overseas. The Company could incur substantial costs in prosecuting or defending trademark infringement suits. If the Company fails to effectively enforce its trademark rights, its competitive position and brand recognition may be diminished.
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Furthermore, the Company's skincare business seeks to establish customer loyalty, in part, by means of its use of trademarks. It can be difficult and costly to defend trademarks from encroachment, especially on the Internet, or misappropriation overseas. Third parties may also challenge the validity of the Company's trademarks. In either eventuality, the Company's customers may become confused and direct their purchases to competitors. Third parties may independently discover trade secrets and proprietary information that allow them to develop technologies and products that are substantially equivalent or superior to the Company's own. Without the protection afforded by the Company's patent, trade secret and proprietary information rights, the Company may face direct competition from others commercializing their products using the Company's technology, which may have a material adverse effect on the Company's business and its prospects. Trade secrets and other proprietary information which are not protected by patents are also critical to the Company's business. The Company attempts to protect its trade secrets by, among other steps, entering into confidentiality agreements with third parties, employees and consultants. However, such other steps may be ineffective, may be found to be invalid by the laws of a particular state or country, and these agreements can be breached and, if they are and even if the Company is able to prove the breach or that its technology has been misappropriated under applicable state law, there may not be an adequate remedy available to the Company.
The Company must monitor and protect its internet domain names to preserve their value. The Company may be unable to prevent third parties from acquiring domain names that are similar to, infringe on or otherwise decrease the value of its trademarks.
Third parties may acquire substantially similar domain names that decrease the value of the Company's domain names and trademarks and other proprietary rights which may hurt its business. Moreover, the regulation of domain names in the United States and foreign countries is subject to change. Governing bodies could appoint additional domain name registrars or modify the requirements for holding domain names. Governing bodies could also establish additional "top-level" domains, which are the portion of the Web address that appears to the right of the "dot," such as "com," "gov" or "org." As a result, the Company may not maintain exclusive rights to all potentially relevant domain names in the United States or in other countries in which the Company conducts business, which could harm its business or reputation.
Claims that the Company misuses the intellectual property of others could subject the Company to significant liability and disrupt its business.
The Company may become subject to material legal proceedings and claims relating to intellectual property matters, including claims of infringement by competitors and other third parties with respect to current or future products, e-commerce and other web-related technologies, online business methods, trademarks, copyrights or other proprietary rights. Its competitors, some of which may have substantially greater resources than the Company has and may have made significant investments in competing products and technologies, may have, or seek to apply for and obtain, patents, copyrights or trademarks that will prevent, limit or interfere with the Company's ability to make, use and sell its current and future products and technologies. The Company may not be successful in defending allegations of infringement of these patents, copyrights or trademarks. Further, the Company may not be aware of all of the patents and other intellectual property rights owned by third parties that may be potentially adverse to its interests. The Company may need to resort to costly and time-consuming litigation to protect and/or enforce its proprietary rights or to determine the scope and validity of a third party's patents or other proprietary rights, including whether any of its products, technologies or processes infringe the patents or other proprietary rights of third parties. Any failure to enforce or protect its rights could cause the Company to lose the ability to exclude others from using its technologies to develop or sell competing products. The Company may incur substantial expenses in defending against third-party infringement claims regardless of the merit of such claims. In addition, while the Company maintains insurance for certain risks, the amount of its insurance coverage may not be adequate to cover the total amount of all insured claims and liabilities. It also is not possible to obtain insurance against all potential risks and liabilities. The outcome of any such proceedings is uncertain and, if unfavorable, could force the Company to discontinue sales of the affected products or impose significant penalties or restrictions on its business. The Company does not conduct comprehensive patent searches to determine whether the technologies used in its products infringe upon patents held by others. In addition, product development is inherently uncertain in a rapidly evolving technological environment in which there may be numerous patent applications pending, many of which are confidential when filed, with regard to similar technologies.
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If the Company is unable to defend its intellectual property rights internationally, it may face increased competition outside the U.S., which could materially and adversely affect its future business, prospects, operating results and financial results and financial condition.
Risks Related to the Company's Regulatory Matters
The Company's failure to obtain and maintain FDA clearances or approvals on a timely basis, or at all, would prevent the Company from commercially distributing and marketing current or upgraded products in the United States, which could severely harm our business.
The Company's products, including the no!no!® family of products, are subject to rigorous regulation by the FDA and numerous other federal, state and foreign governmental authorities. The process of obtaining regulatory clearances or approvals to market a medical device can be costly and time consuming, and we may not be able to obtain these clearances or approvals on a timely basis, if at all. In particular, the FDA permits commercial distribution of a new medical device only after the device has received clearance under Section 510(k) of the Federal Food, Drug and Cosmetic Act or is the subject of an approved premarket approval application, or PMA, unless the device is specifically exempt from those requirements. Should the FDA require, or a change in current regulations occur, that our products be FDA-cleared for marketing and sale in the U.S. we may be required to incur significant expense and engage in a time consuming process seeking such approvals. If we were unable to obtain the required FDA approvals for these products or as necessary to make certain claims about the efficacy of the products, our sales of these products in the U.S. could be materially adversely affected.
The FDA clears marketing of lower-risk medical devices through the 510(k) process if the manufacturer demonstrates that the new product is substantially equivalent to other 510(k)-cleared products. High risk devices deemed to pose the greatest risk, such as life-sustaining, life-supporting, or implantable devices, or devices not deemed substantially equivalent to a previously cleared device, require the pre-market approval (PMA). The PMA process is more costly, and much longer, than the 510(k) clearance process. A PMA application must be supported by extensive data, including, but not limited to, technical, preclinical, clinical trial, manufacturing and labeling data, to demonstrate to the FDA's satisfaction the safety and efficacy of the device for its intended use.
The Company does not currently have any products approved for market through the PMA process. Several products are cleared for market through the 510(k) pathway or are class I products which have been designated as exempt from premarket 510(k) notification requirements. The marketing and sale of our no!no!® family of consumer products in the United States (excluding no!no! Skin and no!no! Glow which have FDA clearance), a market that accounted for approximately 61% of the total sales of this line of products for the year ended December 31, 2013, does not currently require FDA marketing clearance. Accordingly, our no!no!® line of products does not currently have any FDA-cleared indications as to their efficacy in terms of long-term or permanent hair removal or reduction in hair re-growth. Accordingly, we are subject to limitations on the advertising claims we are allowed to make regarding the hair removal and hair reduction effects of our products.
The Company's failure to comply with U.S. federal, state and foreign governmental regulations could lead to the issuance of warning letters or untitled letters, the imposition of injunctions, suspensions or loss of regulatory clearance or approvals, product recalls, or corrective action, termination of distribution, product seizures or civil penalties. In the most extreme cases, criminal sanctions or closure of the manufacturing facility are possible.
If required, clinical trials necessary to support a 510(k) notice or PMA application will be expensive and will require the enrollment of large numbers of patients, and suitable patients may be difficult to identify and recruit. Delays or failures in our clinical trials will prevent us from commercializing any modified or new products and will adversely affect our business, operating results and prospects.
Initiating and completing clinical trials necessary to support a 510(k) notice or a PMA application will be time-consuming and expensive and the outcome uncertain. Moreover, the results of early clinical trials are not necessarily predictive of future results, and any product the Company advances into clinical trials may not have favorable results in early or later clinical trials.
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Conducting successful clinical studies will require the enrollment of large numbers of patients, and suitable patients may be difficult to identify and recruit. Patient enrollment in clinical trials and completion of patient participation and follow-up depend on many factors, including the size of the patient population, the nature of the trial protocol, the attractiveness of, or the discomforts and risks associated with, the treatments received by patients enrolled as subjects, the availability of appropriate clinical trial investigators, support staff, and proximity of patients to clinical sites and ability to comply with the eligibility and exclusion criteria for participation in the clinical trial and patient compliance. For example, patients may be discouraged from enrolling in our clinical trials if the trial protocol requires them to undergo extensive post-treatment procedures or follow-up to assess the safety and effectiveness of our products or if they determine that the treatments received under the trial protocols are not attractive or involve unacceptable risks or discomforts. Patients may also not participate in our clinical trials if they choose to participate in contemporaneous clinical trials of competitive products. In addition, patients participating in clinical trials may die before completion of the trial or suffer adverse medical events unrelated to investigational products.
Development of sufficient and appropriate clinical protocols to demonstrate safety and efficacy may be required and the Company may not adequately develop such protocols to support clearance and approval. Further, the FDA may require the Company to submit data on a greater number of patients than it originally anticipated and/or for a longer follow-up period or change the data collection requirements or data analysis for any clinical trials. Delays in patient enrollment or failure of patients to continue to participate in a clinical trial may cause an increase in costs and delays in the approval and attempted commercialization of our products or result in the failure of the clinical trial. The FDA may not consider our data adequate to demonstrate safety and efficacy. Such increased costs and delays or failures could adversely affect our business, operating results and prospects.
The Company's medical device operations are subject to pervasive and continuing FDA regulatory requirements.
Medical devices regulated by the FDA are subject to "general controls" which include: registration with the FDA; listing commercially distributed products with the FDA; complying with good manufacturing practices under the quality system regulations; filing reports with the FDA of and keeping records relative to certain types of adverse events associated with devices under the medical device reporting regulation; assuring that device labeling complies with device labeling requirements; reporting certain device field removals and corrections to the FDA; and obtaining premarket notification 510(k) clearance for devices prior to marketing. Some devices known as "510(k)-exempt" can be marketed without prior marketing clearance or approval from the FDA. In addition to the "general controls," some Class II medical devices are also subject to "special controls," including adherence to a particular guidance document and compliance with the performance standard. Instead of obtaining 510(k) clearance, some Class III devices are subject to premarket approval (PMA). In general, obtaining premarket approval to achieve marketing authorization from the FDA is a more onerous process than seeking 510(k) clearance.
Many medical devices, such as medical lasers, are also regulated by the FDA as "electronic products." In general, manufacturers and marketers of "electronic products" are subject to certain FDA regulatory requirements intended to ensure the radiological safety of the products. These requirements include, but are not limited to, filing certain reports with the FDA about the products and defects/safety issues related to the products as well as complying with radiological performance standards.
The medical device industry is now experiencing greater scrutiny and regulation by Federal, state and foreign governmental authorities. Companies in our industry are subject to more frequent and more intensive reviews and investigations, often involving the marketing, business practices, and product quality management including standards for device recalls and product labeling. Such reviews and investigations may result in the civil and criminal proceedings; the imposition of substantial fines and penalties; the receipt of Warning Letters, untitled letters, demands for recalls or the seizure of our products; the requirement to enter into corporate integrity agreements, stipulated judgments or other administrative remedies, and result in our incurring substantial unanticipated costs and the diversion of key personnel and management's attention from their regular duties, any of which may have an adverse effect on our financial condition, results of operations and liquidity, and may result in greater and continuing governmental scrutiny of our business in the future.
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The Company must also have the appropriate FDA clearances and/or approvals from other governmental entities in order to lawfully market devices and or/drugs. The FDA, federal, state or foreign governments and agencies may disagree that the Company has such clearance and/or approvals for all of its products and may take action to prevent the marketing and sale of such devices until such disagreements have been resolved.
Additionally, Federal, state and foreign governments and entities have enacted laws and issued regulations and other standards requiring increased visibility and transparency of our Company's interactions with healthcare providers. For example, the U.S. Physician Payment Sunshine Act requires us to disclose payments and other transfers of value to all U.S. physicians and U.S. teaching hospitals at the U.S. federal level made after August 1, 2013. Failure to comply with these legal and regulatory requirements could impact our business, and we have had and will continue to spend substantial time and financial resources to develop and implement enhanced structures, policies, systems and processes to comply with these legal and regulatory requirements, which may also impact our business.
Healthcare policy changes may have a material adverse effect on the Company.
Healthcare costs have risen significantly over the past decade. As a result, there have been and continue to be proposals Federal, state and foreign governments and regulators as well as third-party insurance providers to limit the growth of these costs. Among these proposals are regulations that could impose limitations on the prices the Company will be able to charge for its products, the amounts of reimbursement available for its products from governmental agencies or third-party payors, requirements regarding the usage of comparative studies, technology assessments and healthcare delivery structure reforms to determine the effectiveness and select the products and therapies used for treatment of patients. While we believe our products provide favorable clinical outcomes, value and cost efficiency, the resources necessary to demonstrate this value to our customers, patients, payors, and regulators is significant and may require longer periods of time and effort in which to obtain acceptance of our products. There is no assurance that our efforts will be successful, and these limitations could have a material adverse effect on the Company's financial position and results of operations.
These changes and additional proposed changes in the future could adversely affect the demand for the Company's products as well as the way in which the Company conducts its business. For example, the Patient Protection and Affordable Care Act and Health Care and Education Affordability Reconciliation Act of 2010 were enacted into law in the U.S. in March 2010. The law imposed on medical device manufacturers a 2.3 percent excise tax on U.S. sales of Class I, II and III medical devices beginning in January 2013, which includes certain products marketed and sold by the Company, as well as requiring research into the effectiveness of treatment modalities and instituting changes to the reimbursement and payment systems for patient treatments. In addition, governments and regulatory agencies continue to study and propose changes to the laws governing the clearance or approval, manufacture and marketing of medical devices, which could adversely affect our business and results of operations.
FDA regulations and guidance are often revised or reinterpreted by the FDA in ways that may significantly affect our business and our products. The FDA is currently exploring ways to modify its 510(k) clearance process. In addition, due to changes at the FDA in general, it has become increasingly more difficult to obtain 510(k) clearance as data requirements have increased. It is impossible to predict whether legislative changes will be enacted or FDA regulations, guidance or interpretations changed, and what the impact of such changes, if any, may be. However, any changes could make it more difficult for the Company to maintain or attain clearance or approval to develop and commercialize our products and technologies.
Various healthcare reform proposals have also emerged at the state level. The Company cannot predict what healthcare initiatives, if any, will be implemented at the federal or state level, or the effect any future legislation or regulation will have on the Company. However, an expansion in government's role in the U.S. healthcare industry may lower reimbursements for the Company's products, reduce medical procedure volumes and adversely affect the Company's business, possibly materially. In addition, if the excise taxes contained in the House or Senate health reform bills are enacted into law, the Company's operating expenses resulting from such an excise tax and results of operations would be materially and adversely affected.
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If the effectiveness and safety of the Company's devices are not supported by long-term data, the Company's revenues could decline.
The Company's products may not be accepted in the market if the Company does not produce clinical data supported by the independent efforts of clinicians. The Company received clearance from the FDA for the use of the XTRAC system to treat psoriasis based upon the Company's study of a limited number of patients. Safety and efficacy data presented to the FDA for the XTRAC system was based on studies on these patients. For the treatment of vitiligo, atopic dermatitis and leukoderma, the Company has received clearance from the FDA for the use of the XTRAC system based primarily on a showing of substantial equivalence to other previously cleared predicate devices. However, the Company may discover that physicians will expect clinical data on such treatments with the XTRAC system. The Company also may find that data from longer-term psoriasis patient follow-up studies may be inconsistent with those indicated by the Company's relatively short-term data. If longer-term patient studies or clinical experience indicate that treatment with the XTRAC system does not provide patients with sustained benefits or that treatment with the Company's product is less effective or less safe than the Company's current data suggests, the Company's revenues could decline. In addition, the FDA could then bring legal or regulatory enforcement actions against the Company and/or its products including, but not limited to, recalls or requirements for pre-market 510(k) authorizations. The Company can give no assurance that its data will be substantiated in studies involving more patients. In such a case, the Company may never achieve significant revenues or profitability.
Certain indications for use for the PTL light-based products are permitted in Europe and elsewhere in the world, but are not approved or cleared for marketing in the U.S. Such approvals/clearances in the U.S. could be costly and take significant time to obtain. If the Company is ultimately not approved or cleared to market the devices for these additional indications for use in the U.S., it is uncertain whether the products will be successful in the U.S.
If the Company is found to be promoting the use of its devices for unapproved or "off-label" uses or engaging in other noncompliant activities, the Company may be subject to recalls, seizures, fines, penalties, injunctions, adverse publicity, prosecution, or other adverse actions, resulting in damage to its reputation and business.
The Company's labeling, advertising, promotional materials and user training materials must comply with the FDA and other applicable laws and regulations, including the prohibition of the promotion of a medical device for a use that has not been cleared or approved by the FDA. Obtaining 510(k) clearance or PMA approval only permits the Company to promote its products for the uses specifically cleared by the FDA. Use of a device outside its cleared or approved indications is known as "off-label" use. Physicians and consumers may use the Company's products off-label because the FDA does not restrict or regulate a physician's choice of treatment within the practice of medicine nor is there oversight on patient use of over-the-counter devices. Although the Company may request additional cleared indications for our current products, the FDA may deny those requests, require additional expensive clinical data to support any additional indications or impose limitations on the intended use of any cleared product as a condition of clearance. Even if regulatory clearance or approval of a product is granted, such clearance or approval may be subject to limitations on the intended uses for which the product may be marketed and reduce our potential to successfully commercialize the product and generate revenue from the product.
If the FDA determines that the Company's labeling, advertising, promotional materials, or user training materials, or representations made by Company personnel, include the promotion of an off-label use for the device, or that the Company has made false or misleading or inadequately substantiated promotional claims, or claims that could potentially change the regulatory status of the product, the agency could take the position that these materials have misbranded the Company's devices and request that the Company modifies its labeling, advertising, or user training or promotional materials and/or subject the Company to regulatory or legal enforcement actions, including the issuance of an Untitled Letter or a Warning Letter, injunction, seizure, recall, adverse publicity, civil penalties, criminal penalties, or other adverse actions. It is also possible that other federal, state, or foreign enforcement authorities might take action if they consider the Company's labeling, advertising, promotional, or user training materials to constitute promotion of an unapproved use, which could result in significant fines, penalties, or other adverse actions under other statutory authorities, such as laws prohibiting false claims for reimbursement. In that event, we would be subject to extensive fines and penalties and the Company's reputation could be damaged and adoption of the products would be impaired. Although the Company intends to refrain from statements that could be considered off-label promotion of its products, the FDA or another regulatory agency could disagree and conclude

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that the Company has engaged in off-label promotion. For example, the Company has made statements regarding some of its devices that the FDA may view as off-label promotion. In addition, any such off-label use of the Company's products may increase the risk of injury to patients, and, in turn, the risk of product liability claims, and such claims are expensive to defend and could divert the Company's management's attention and result in substantial damage awards against the Company.
The Company currently markets the no!no!® product for hair removal. Based on previous feedback received from the FDA, this product is not considered a medical device so long as the Company does not promote the product for medical claims. Promotion of this product for claims beyond those agreed upon by the FDA may subject the product to regulation by the FDA, and may require clearance of a 510(k) notice to continue marketing the product.
The Company may be subject, directly or indirectly, to federal and state healthcare fraud and abuse laws and regulations and could face substantial penalties if the Company is unable to fully comply with such laws.
While the Company does not control referrals of healthcare services or bill directly to Medicare, Medicaid or other third-party payors, many healthcare laws and regulations apply to the Company's business. For example, the Company could be subject to healthcare fraud and abuse and patient privacy regulation and enforcement by both the federal government and the states in which the Company conducts its business. The healthcare laws and regulations that may affect the Company's ability to operate include:
the federal healthcare programs' Anti-Kickback Law, which prohibits, among other things, persons or entities from soliciting, receiving, offering or providing remuneration, directly or indirectly, in return for or to induce either the referral of an individual for, or the purchase order or recommendation of, any item or service for which payment may be made under a federal healthcare program such as the Medicare and Medicaid programs;
federal false claims laws which prohibit, among other things, individuals or entities from knowingly presenting, or causing to be presented, claims for payment from Medicare, Medicaid, or other third-party payors that are false or fraudulent, or are for items or services not provided as claimed and which may apply to entities like the Company to the extent that the Company's interactions with customers may affect their billing or coding practices;
the federal Health Insurance Portability and Accountability Act of 1996, or HIPAA, which established new federal crimes for knowingly and willfully executing a scheme to defraud any healthcare benefit program or making false statements in connection with the delivery of or payment for healthcare benefits, items or services, as well as leading to regulations imposing certain requirements relating to the privacy, security and transmission of individually identifiable health information; and
state law equivalents of each of the above federal laws, such as anti-kickback and false claims laws which may apply to items or services reimbursed by any third-party payor, including commercial insurers, and state laws governing the privacy of health information in certain circumstances, many of which differ from each other in significant ways and often are not preempted by HIPAA, thus complicating compliance efforts.
Recently, the medical device industry has been under heightened scrutiny as the subject of government investigations and regulatory or legal enforcement actions involving manufacturers who allegedly offered unlawful inducements to potential or existing customers in an attempt to procure their business, including arrangements with physician consultants. If the Company's operations or arrangements are found to be in violation of any of the laws described above or any other governmental regulations that apply to the Company, the Company may be subject to penalties, including civil and criminal penalties, damages, fines, exclusion from the Medicare and Medicaid programs and the curtailment or restructuring of its operations. Any penalties, damages, fines, exclusions, curtailment or restructuring of the Company's operations could adversely affect its ability to operate its business and its financial results. The risk of the Company being found in violation of these laws is increased by the fact that

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many of these laws are broad and their provisions are open to a variety of interpretations. Any action against the Company for violation of these laws, even if the Company successfully defends against that action and the underlying alleged violations, could cause the Company to incur significant legal expenses and divert its management's attention from the operation of its business. If the physicians or other providers or entities with whom the Company does business are found to be non-compliant with applicable laws, they may be subject to sanctions, which could also have a negative impact on the Company's business.
The Company or its subsidiaries' failure to obtain or maintain necessary FDA clearances or approvals, or equivalents thereof in the U.S. and relevant foreign markets, could hurt our ability to distribute and market our products.
In both the Company's and its subsidiaries' United States and foreign markets, the Company and its subsidiaries are affected by extensive laws, governmental regulations, administrative determinations, court decisions and similar constraints. Such laws, regulations and other constraints may exist at the federal, state or local levels in the United States and at analogous levels of government in foreign jurisdictions.
For example, the Company's laser products are considered medical devices and are subject to extensive regulation in the U.S. and in foreign countries where we intend to do business. In addition, certain of the Company's skincare products and product candidates may fall under the regulatory purview of various centers at the FDA and in other countries by similar health and regulatory authorities. As the Company seeks to expand sales of its skincare products outside the U.S., we may encounter requirements that we did not anticipate or that we may not be able to satisfy.
In addition, the formulation, manufacturing, packaging, labeling, distribution, importation, sale and storage of the Company's and its subsidiaries' products are subject to extensive regulation by various federal agencies, including, but not limited to, the FDA, the FTC, State Attorneys General in the United States, the Ministry of Health, Labor and Welfare in Japan, as well as by various other federal, state, local and international regulatory authorities in the countries in which its products are manufactured, distributed or sold. If the Company or its manufacturers fail to comply with those regulations, the Company and its subsidiaries could become subject to significant penalties or claims, which could harm its results of operations or its ability to conduct its business. In addition, the adoption of new regulations or changes in the interpretations of existing regulations may result in significant compliance costs or discontinuation of product sales and may impair the marketing of its products, resulting in significant loss of net sales. The Company's failure to comply with federal or state regulations, or with regulations in foreign markets that cover its product claims and advertising, including direct claims and advertising by the Company or its subsidiaries, may result in enforcement actions and imposition of penalties or otherwise harm the distribution and sale of its products. Further, the Company and its subsidiaries' businesses are subject to laws governing our accounting, tax and import and export activities. Failure to comply with these requirements could result in legal and/or financial consequences that might adversely affect its sales and profitability.  Each medical device that the Company wishes to market in the U.S. must first receive either 510(k) clearance or premarket approval from the FDA unless an exemption applies. Either process can be lengthy and expensive. The FDA's 510(k) clearance process may take from three to twelve months, or longer, and may or may not require human clinical data. The premarket approval process is much more costly and lengthy. It may take from eleven months to three years, or even longer, and will likely require significant supporting human clinical data. Delays in obtaining regulatory clearance or approval could adversely affect the Company's revenues and profitability. Although the Company has obtained 510(k) clearances for its XTRAC system for use in treating psoriasis, vitiligo, atopic dermatitis and leukoderma, and 510(k) clearances for its Omnilux devices as well as extensive 510(k) clearances for its surgical products, these clearances may be subject to revocation if post-marketing data demonstrates safety issues or lack of effectiveness. Similar clearance processes may apply in foreign countries. Further, more stringent regulatory requirements or safety and quality standards may be issued in the future with an adverse effect on the Company's business.
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Although cosmetic products are not subject to any FDA premarket approval or clearance process, they must, nonetheless, comply with the FDA's formulation, manufacturing and labeling requirements or such products may be considered adulterated or misbranded by the agency which could subject the Company to potential regulatory or legal enforcement actions. Similar, or more stringent, requirements may apply in foreign jurisdictions as well.  The Company may also find that if its cosmetic products compete with a third-party's drug product, competitive and regulatory pressure may be applied against the cosmetic products. Some cosmetic products may be viewed by the FDA or international regulatory agencies as drugs or devices to a large extent based upon the promotional claims or ingredients. Because there is a degree of subjectivity in determining whether marketing materials or statements constitute product claims and whether they involve drug claims, the Company's claims and interpretation of applicable regulations may be challenged, which could harm its business.
Sunscreen products that contain ingredients or make claims beyond those identified by the FDA in its sunscreen monograph and corresponding guidance documents are considered over-the-counter drugs. The cosmetics containing sunscreen ingredients are required to conform with the FDA's sunscreen monograph as well as other international regulatory requirements for sunscreen products. The FDA may view some of the Company's sunscreen products as new drugs if the FDA determines that its formula and/or claims are not in compliance with the monograph or applicable guidance. In addition, certain countries may impose additional regulatory requirements upon these products in order for these products to be marketed and sold in those countries.
Certain indications for use for the Company's PTL light-based products are permitted in Europe and elsewhere in the world, but are not cleared or approved for marketing in the U.S. Such clearances or approvals could be costly and take significant time to obtain. If the Company is not approved or cleared to market the indications for use in the U.S., it is uncertain whether the products will be successful in the U.S.
The Company has modified some of its products and sold them under prior 510(k) clearances. The FDA could decide the modifications required new 510(k) clearances and require the Company to cease marketing and/or recall the modified products.
Any modification to one of the Company's 510(k) cleared devices that could significantly affect its safety or effectiveness, or that would constitute a major change in its intended use, requires a new 510(k) clearance or a pre-market approval. The Company may be required to submit pre-clinical and clinical data dependingcontinued listing on the natureNasdaq Capital Market under Marketplace Rule 5550(a)(2). The notice provides us with an initial period of 180 calendar days, or until August 19, 2018, to regain compliance with the changes andlisting rules. We will regain compliance if the product. The Company may not be able to obtain additional 510(k) clearances or pre-market approvals for modifications to, or additional indications for, its existing products in a timely fashion, or at all. Delays in obtaining future clearances or approvals would adversely affect its ability to introduce new or enhanced products into the market in a timely manner, which in turn would harm its revenue and operating results. The Company has modified some of its marketed devices, but the Company has determined, and may make such additional determinations in the future, that new 510(k) clearances or pre-market approvals are not required.  The FDA requires every manufacturer to make this determination in the first instance, but the FDA may review the manufacturer's decision. The Company cannot be certain that the FDA would agree with any of its prior or future decisions not to seek new 510(k) clearances or pre-market approvals. If the FDA requires the Company to seek new 510(k) clearance or a pre-market approval for any modification, the Company also may be required to cease marketing, distributions and/or recall the modified device until the Company obtains such 510(k) clearance or pre-market approval, and may be subject to significant regulatory fines or penalties. The FDA could also bring legal or regulatory enforcement action against the Company or its products.
Any recall or FDA requirement that the Company seek additional approvals or clearances could result in significant delays, fines, increased costs associated with modification of a product, loss of revenue and potential operating restrictions imposed by the FDA. New submissions to obtain 510(k) clearance or PMA approval could require additional pre-clinical and/or clinical testing which could be expensive and time consuming.
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There is no guarantee that the FDA will grant 510(k) clearance or PMA approvalclosing bid price of our future products and failure to obtain necessary clearancescommon stock is $1.00 per share or approvalshigher for our future products would adversely affect our ability to grow our business.
Somea minimum period of the Company's new or modified products may require the FDA clearance of a 510(k) notice. In addition some of the products may require clinical trials to support regulatory approval and we may not successfully complete these clinical trials. The FDA may not approve or clear these products for the indications that are necessary or desirable for successful commercialization. Indeed, the FDA may refuse requests for 510(k) clearance or premarket approval of new products. Failure to receive clearance or approval for new products would have an adverse effect on the Company's ability to expand our business.
The results of the Company's clinical trials may not support our product candidate claims or may result in the discovery of adverse side effects.
Even if any of the Company's clinical trials are completedten consecutive business days during this compliance period, as planned, it cannot be certain that study results will support product candidate claims or that the FDA or foreign regulatory authorities will agree with our conclusions regarding them. Success in pre-clinical evaluation and early clinical trials does not ensure that later clinical trials will be successful, and we cannot be sure that the later trials will replicate the results of prior trials and pre-clinical studies. The clinical trial process may fail to demonstrate that our product candidates are safe and effective for the proposed indicated uses, which could cause us to abandon a product candidate and may delay development of others. Any delay or termination of our clinical trials will delay the filing of our product submissions and, ultimately, our ability to commercialize our product candidates and generate revenues. It is also possible that patients enrolled in clinical trials will experience adverse side effects that are not currently part of the product candidate's profile.
The Company's market acceptance in international markets requires regulatory approvalsconfirmed by written notification from foreign governments and may depend on third party reimbursement of participants' cost.
The Company has introduced its XTRAC system into markets in more than 30 countries in Europe, the Middle East, the Far East Asia, Southeast Asia, Australia, South Africa and parts of Central and South America. The Company intends to expand the number of countries in these markets where the Company distributes its products through the network of distributors which PTL and GlobalMed have built. The Company cannot be certain that its distributors will be successful in marketing XTRAC systems in these or other countries or that its distributors will purchase XTRAC systems beyond their current contractual obligations or in accordance with the Company's expectations.
Even if the Company obtains and maintains the necessary foreign regulatory registrations or approvals, market acceptance of the Company's products in international markets may be dependent, in part, upon the availability of reimbursement within applicable healthcare payment systems. Reimbursement and healthcare payment systems in international markets vary significantly by country, and include both government-sponsored healthcare and private insurance. The Company may seek international reimbursement approvals for its products, but the Company cannot assure you that any such approvals will be obtained in a timely manner, if at all. Failure to receive international reimbursement approvals in any given market could have a material adverse effect on the acceptance or growth of the Company's products in that market or others.
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If the Company or its third-party manufacturers or suppliers fail to comply with the FDA's Quality System Regulation or any applicable state equivalent, the Company's manufacturing operations could be interrupted and the Company's potential product sales and operating results could suffer.
The Company and some of its third-party manufacturers and suppliers are required to comply with some or all of the FDA's drug Good Manufacturing Practices or its QSR, which delineates the design controls, document controls, purchasing controls, identification and traceability, production and process controls, acceptance activities, nonconforming product requirements, corrective and preventive action requirements, labeling and packaging controls, handling, storage, distribution and installation requirements, records requirements, servicing requirements, and statistical techniques potentially applicable to the production of the Company's medical devices. The Company and its manufacturers and suppliers are also subject to the regulations of foreign jurisdictions regarding the manufacturing process if the Company markets its products overseas. The FDA enforces the QSR through periodic and announced or unannounced inspections of manufacturing facilities. The Company's facilities have been inspected by the FDA and other regulatory authorities, and the Company anticipates that it and certain of its third-party manufacturers and suppliers will be subject to additional future inspections. If the Company's facilities or those of its manufacturers or suppliers are found to be in non-compliance or fail to take satisfactory corrective action in response to adverse QSR inspectional findings, FDA could take legal or regulatory enforcement actions against the Company and/or its products, including but not limited to the cessation of sales or the recall of distributed products, which could impair the Company's ability to produce its products in a cost-effective and timely manner in order to meet its customers' demands. The Company may also be required to bear other costs or take other actions that may have a negative impact on its future sales and its ability to generate profits.
Current regulations depend heavily on administrative interpretation. If the FDA does not believe that the Company is in substantial compliance with applicable FDA regulations, the agency could take legal or regulatory enforcement actions against the Company and/or its products. The Company is also subject to periodic inspections by the FDA, other governmental regulatory agencies, as well as certain third-party regulatory groups. Future interpretations made by the FDA or other regulatory bodies made during the course of these inspections may vary from current interpretations and may adversely affect the Company's business and prospects. The FDA's and foreign regulatory agencies' statutes, regulations, or policies may change, and additional government regulation or statutes may be enacted, which could increase post-approval regulatory requirements, or delay, suspend, prevent marketing of any cleared / approved products or necessitate the recall of distributed products. The Company cannot predict the likelihood, nature or extent of adverse governmental regulation that might arise from future legislative or administrative action, either in the U.S. or abroad.
Recently, the medical device industry has been under heightened FDA scrutiny as the subject of government investigations and enforcement actions. If the Company's operations and activities are found to be in violation of any FDA laws or any other governmental regulations that apply to the Company, the Company may be subject to penalties, including civil and criminal penalties, damages, fines and other legal and/or agency enforcement actions. Any penalties, damages, fines, or curtailment or restructuring of the Company's operations or activities could adversely affect its ability to operate its business and its financial results. The risk of the Company being found in violation of FDA laws is increased by the fact that many of these laws are broad and their provisions are open to a variety of interpretations. Any action against the Company for violation of these laws, even if the Company successfully defends against that action and its underlying allegations, could cause the Company to incur significant legal expenses and divert its management's attention from the operation of its business. Where there is a dispute with a federal or state governmental agency that cannot be resolved to the mutual satisfaction of all relevant parties, the Company may determine that the costs, both real and contingent, are not justified by the commercial returns to the Company from maintaining the dispute or the product.
Various claims, design features or performance characteristics of Company drugs, medical devices and cosmetic products, that the Company regarded as permitted by the FDA without marketing clearance or approval, may be challenged by the FDA or state regulators. The FDA or state regulatory authorities may find that certain claims, design features or performance characteristics, in order to be made or included in the products, may have to be supported by further studies and marketing clearances or approvals, which could be lengthy, costly and possibly unobtainable.
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The Lumiere Excel and Lumiere Spa products are LED therapy products sold to tanning salons and spas. In 2011, the Texas Department of State Health Services (DSHS) challenged the Company's and its customers' right to make certain marketing claims for its Lumiere LED products. Texas DSHS had requested that the Company seek FDA feedback on the regulatory/marketing status of the Lumiere products. Prior to the Company engaging the FDA on this topic, the FDA issued a December 21, 2011 letter to the Indoor Tanning Association indicating that products, similar to the Lumiere, require 510(k) clearance, despite the fact that the FDA issued a November 18, 2004 letter stating that the Lumiere did not require 510(k) clearance. In March, 2012, the Company sent letters to all Lumiere customers throughout the United States, requested that they discontinue using any promotional literature made by PhotoMedex that includes therapeutic claims for red-light therapy now prohibited by the FDA (as described in the letter from FDA to the Indoor Tanning Association). The Company has, as of February 2012, suspended the marketing of, and shipments of Lumiere throughout the United States. It is unlikely the Company will obtain OTC 510(k) clearance within the near future.
The Company has no outstanding Warning Letters from the FDA. In February 2015, the Company met with the FDA at an administrative action meeting regarding certain aspects of the labeling for the Iamin family of medical devices. The FDA has requested that the labeling be amended to more closely mirror the language of the products' 510(k) clearances, The Company has voluntarily halted distribution of this particular product group and has implemented corrective action to implement these changes, which it anticipates will be completed during the Second Quarter of 2015, at which time distribution of these products will resume.
The FDA determines whether a product is a cosmetic or a drug to a large extent based upon the claims made for the product. Because there is a degree of subjectivity in determining whether marketing materials or statements constitute product claims and whether they involve improper drug claims, our claims and our interpretation of applicable regulations may be challenged, which could harm our business.
If the Company fails to comply with ongoing regulatory requirements, or if it experiences unanticipated problems with products, these products could be subject to restrictions or withdrawal from the market.
The Company is also subject to similar state requirements and licenses. Failure by the Company to comply with statutes and regulations administered by the FDA and other regulatory bodies, discovery of previously unknown problems with its products (including unanticipated adverse events or adverse events of unanticipated severity or frequency), manufacturing problems, or failure to comply with regulatory requirements, or failure to adequately respond to any FDA observations concerning these issues, could result in, among other things, any of the following actions:
warning letters or untitled letters issued by the FDA;
fines, civil penalties, injunctions and criminal prosecution;
unanticipated expenditures to address or defend such actions;
delays in clearing or approving, or refusal to clear or approve, our products;
withdrawal or suspension of clearance or approval of our products by the FDA or other regulatory bodies;
product recall or seizure;
orders for physician or customer notification or device repair, replacement or refund;
interruption of production; and
operating restrictions.
If any of these actions were to occur, it would harm the Company's reputation and adversely affect its business, financial condition and results of operations.
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The Company's medical products may in the future be subject to product recalls that could harm its reputation, business and financial results.
The FDA has the authority to require the recall of commercialized medical device products in the event of material deficiencies or defects in design or manufacture. In the case of the FDA, the authority to require a recall must be based on an FDA finding that there is a reasonable probability that the device would cause serious injury or death. Manufacturers may, under their own initiative, recall a product if any material deficiency in a device is found. A government-mandated or voluntary recall by the Company or one of its distributors could occur as a result of component failures, manufacturing errors, design or labeling defects or other deficiencies and issues. Recalls of any of the Company's products would divert managerial and financial resources and have an adverse effect on its financial condition and results of operations. The FDA requires that certain classifications of recalls be reported to the FDA within ten (10) working days after the recall is initiated. Companies are required to maintain certain records of recalls, even if they are not reportable to the FDA. The Company may initiate voluntary recalls involving its products in the future that the Company determines do not require notification of the FDA. If the FDA disagrees with the Company's determinations, they could require the Company to report those actions as recalls. A future recall announcement could harm the Company's reputation with customers and negatively affect its sales. In addition, the FDA could take enforcement action for failing to report the recalls when they were conducted. No recalls of the Company's medical products have been reported to the FDA.
If the Company's medical products cause or contribute to a death or a serious injury, or malfunction in certain ways, we will be subject to medical device reporting regulations, which can result in voluntary corrective actions or agency enforcement actions.
Under the FDA medical device reporting regulations, medical device manufacturers are required to report to the FDA information that a device has or may have caused or contributed to a death or serious injury or has malfunctioned in a way that would likely cause or contribute to death or serious injury if the malfunction of the device or one of our similar devices were to recur. If the Company fails to report these events to the FDA within the required timeframes, or at all, the FDA could take enforcement action against the Company. Any such adverse event involving its products also could result in future voluntary corrective actions, such as recalls or customer notifications, or agency action, such as inspection or enforcement action. Any corrective action, whether voluntary or involuntary, as well as defending ourselves in a lawsuit, will require the dedication of the Company's time and capital, distract management from operating our business, and may harm its reputation and financial results.
Risk Factors Relating to Acquisition or Merger of other entities
The business operations of PhotoMedex and any other company acquired by or merged into PhotoMedex (the "target company") in the future may not be successfully integrated and therefore PhotoMedex may not be able to realize the anticipated benefits of the acquisition or merger.
Realization of the anticipated benefits of an acquisition or merger will depend on PhotoMedex's ability to successfully integrate the businesses and operations of PhotoMedex and the target company. PhotoMedex will be required to devote significant management attention and resources to integrating its business practices, operations and support functions. The challenges we may encounter include the following:
preserving customer, supplier and other important relationships and resolving potential conflicts that may arise as a result of the merger;
consolidating and integrating duplicative facilities and operations, including back-office systems necessary for internal and disclosure controls and timely financial reporting;
addressing differences in business cultures, preserving employee morale and retaining key employees while maintaining focus on providing consistent, high-quality customer service and meeting the operational and financial goals of the Company; and
adequately addressing business integration issues.
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The process of integrating the target company's operations could cause an interruption of, or loss of momentum in, PhotoMedex's business and financial performance, and in the business and financial performance of the target company as well. The diversion of management's attention and any delays or difficulties encountered in connection with the merger or acquisition and the integration of the two companies' operations could have an adverse effect on the business, financial results, financial condition, or stock price of PhotoMedex. The integration process may also result in additional and unforeseen expenses. There can be no assurance that the contemplated operating efficiencies, synergies in technology, and cross-benefits in sales and marketing activities anticipated from the merger will be realized.
The ability of PhotoMedex and/or the target company to use their net operating loss carryforwards to offset future taxable income.
The ability of PhotoMedex and/or the target company to use their net operating loss carryforwards to offset future taxable income for U.S. federal income, U.K. business or another country's business or income tax purposes may be limited as a result of "ownership changes" of PhotoMedex or the target company caused by the merger. In addition, the amount of such NOL carryforwards could be subject to adjustment in the event of an IRS examination.
With regard to U.S. federal income taxation, if a corporation undergoes an "ownership change" under Section 382 of the U.S. Internal Revenue Code, the amount of its pre-change net operating losses, which we refer to in this report as "NOLs" that may be utilized to offset future taxable income is subject to an annual limitation. In general, an ownership change occurs if the aggregate stock ownership of certain stockholders increases by more than 50 percentage points over such stockholders' lowest percentage ownership during the applicable testing period (generally three years).
The annual limitation generally is determined by multiplying the value of the corporation's stock immediately before the ownership change by the applicable long-term tax-exempt rate. Any unused annual limitation may, subject to certain limits, be carried over to later years, and the limitation may under certain circumstances be increased by recognized built-in gains or reduced by recognized built-in losses in the assets held by the corporation at the time of the ownership change.
In addition, the amount of the NOL carryforwards is subject to review and audit by the Internal Revenue Service (the "IRS"). There can therefore be no assurance that the benefit of such NOL carryforwards will be fully realized.
Likewise, if a corporation undergoes an "ownership change" and/or a "change in trade or business" under various standards of Her Majesty's Revenue and Customs (HMRC, U.K.), the amount of a company's pre-change NOLs that may be utilized to offset future taxable income in the U.K. may be limited or not available for offset against that income.
Similar rules and limitations may apply for U.S. state income tax purposes or for the purposes of other countries' business or income taxes.
PhotoMedex may incur substantial expenses related to any merger or acquisition and the integration of the target company's business operations.
PhotoMedex may incur substantial expenses related to any acquisition or merger, both in connection with the acquisition or merger and in the integration of the target company's business operations into PhotoMedex, both in the year of acquisition or merger and in subsequent years. There are a large number of processes, policies, procedures, operations, technologies and systems that may need to be integrated, including purchasing, accounting and finance, sales, payroll, pricing, revenue management, marketing and benefits. While a certain level of expenses may be assumed to be incurred in any acquisition or merger, there are many factors beyond PhotoMedex's control that could affect the total amount or the timing of such integration expenses. Moreover, many of the expenses that may be incurred are, by their nature, difficult to estimate accurately. Such expenses may also continue for several years following the acquisition or merger, due to ongoing transitions and processes. These expenses could, particularly in the near term, exceed the savings that PhotoMedex expects to achieve from the elimination of duplicative expenses and the realization of economies of scale and cost savings in any acquisition or merger.
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The need to integrate PhotoMedex's and the target company's respective workforces and other factors of production and distribution following the merger presents the potential for delay in achieving expected efficiencies, synergies and other cross-benefits that could adversely affect PhotoMedex's operations.
The successful integration of any target company and achievement of the anticipated benefits of an acquisition or merger depend in part on integrating the target company's and PhotoMedex's employees into a mutually tolerant, collaborative and cross-pollinating team. Failure to do so presents the potential for delays in achieving expected synergies and other benefits of integration that could adversely affect both PhotoMedex's and the target company's operations.
PhotoMedex or the target company may be unable to retain key employees.
The success of PhotoMedex following any acquisition or merger will depend in part upon its ability to retain key employees of PhotoMedex and the target company. Key employees may depart because of issues relating to the uncertainty and difficulty of any remaining integration issues or a desire not to remain with PhotoMedex or the target company following the merger. Accordingly, no assurance can be given that PhotoMedex and the target company would be able to retain key employees to the same extent as prior to the acquisition or merger.
Risk Factors Relating to the Company's Senior Secured Credit Facilities

PhotoMedex's failure to comply with the covenants contained in its senior credit facilities, including as a result of events beyond our control, could materially and adversely affect our operating results and our financial condition.

PhotoMedex entered into an $85 million senior secured credit facilities ("the Facilities") with JP Morgan Chase ("Chase") on May 12, 2014. The facilities are secured by a first priority security interest in and lien on all assets of the Company. All current and future subsidiaries are guarantors on the facilities. Those facilities require us to maintain certain financial ratios; as of December 31, 2014, PhotoMedex remains in default of the credit facilities. While the Company and its creditors have agreed to the terms of a second Amended and Restated Forbearance Agreement, there is no guarantee that such forbearance will continue beyond the terms of the current agreement. If the Company does not cure those defaults and otherwise satisfy the terms of the existing Forbearance Agreement, the holders of the defaulted debt could cause all amounts outstanding with respect to that debt to be due and payable immediately. We cannot assure you that our assets or cash flow would be sufficient to fully repay borrowings under the outstanding facilities or that we would be able to refinance or restructure the payments on those facilities.
If, in the future, PhotoMedex is required to obtain similar forbearance agreements as a result of our inability to meet the terms of the credit agreement, there can be no assurance that those forbearance agreements will be available on commercially reasonable terms or at all. If, as or when required, we are unable to repay, refinance or restructure our indebtedness under those credit facilities, or amend the covenants contained therein, the lenders could elect to terminate their commitments under the credit facilities and institute foreclosure proceedings against our assets. Under such circumstances, we could be forced into bankruptcy or liquidation. In addition, any additional events of default or declaration of acceleration under one of those facilities or the forbearance agreement could also result in an event of default under one or more of these agreements. Such a declaration would have a material adverse impact on our liquidity, financial position and results of operations.

Our level of debt makes us more sensitive to the effects of economic downturns; our level of debt and provisions in our debt agreements could limit our ability to react to changes in the economy or our industry.
Our level of debt makes us more vulnerable to changes in our results of operations because a substantial portion of our cash flow from operations is dedicated to servicing our debt and is not available for other purposes. Our level of debt could have other negative consequences to us, including the following:
·Limiting our ability to borrow money or sell stock for our working capital, capital expenditures, debt service requirements or other general corporate purposes;
·Limiting our flexibility in planning for, or reacting to, changes in our operations, our business or the industry in which we compete;
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·Our leverage may place us at a competitive disadvantage by limiting our ability to invest in the business or in further research and development.
Our ability to make payments on our indebtedness depends on our ability to generate cash in the future. Nasdaq.

If we do not generate sufficient cash flowachieve compliance by August 19, 2018, we expect that Nasdaq would provide notice that our securities are subject to meet our debt service and working capital requirements, we may need to seek additional financing or sell assets. This may make it more difficult for us to obtain financing on terms that are acceptable to us, or at all. Without any such financing, we could be forced to sell assets to make up for any shortfall in our payment obligations under unfavorable circumstances. If necessary, we may not be able to sell assets quickly enough or for sufficient amounts to enable us to meet our obligations.

In addition, our credit facilities anddelisting from the forbearance agreement contain covenants that limit our flexibility in planning for or reacting to changes in our business and our industry, including limitations on incurring additional indebtedness, making investments, granting liens and merging or consolidating with other companies. Complying with these covenants may impair our ability to finance our future operations or capital needs or to engage in other favorable business activities.

Risk Factors Relating to an Investment in our Securities
Potential fluctuations in the Company's operating results could lead to fluctuations in the market price for the Company's common stock.
The Company's results of operations are expected to fluctuate significantly from quarter to quarter, depending upon numerous factors, including:
the present macro-economic uncertainty in the global economy and financial industry and governmental monetary and fiscal programs to stimulate better economic conditions;
healthcare reform and reimbursement policies;
demand for the Company's products;
changes in the Company's pricing policies or those of its competitors;
increases in the Company's manufacturing costs;
the number, timing and significance of product enhancements and new product announcements by the Company and its competitors;
the termination or expiration of significant royalty-generating licensing contracts to which the Company is party;
the expiration of certain of the Company's patents, the issuance of certain the Company's patent applications, and/or if certain of the Company's patent applications fail to issue and prosecution has terminated;
The Company's ability to develop, introduce and market new and enhanced versions of its products on a timely basis considering, among other things, delays associated with the FDA and other regulatory approval processes and the timing and results of future clinical trials;
Acts of terrorism in Israel or in other countries in which we do business;
developments in existing or new litigation; and
product quality problems, personnel changes and changes in the Company's business strategy.
Variations in the above operating factors could lead to significant fluctuations in the market price of the Company's stock.
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The Company'sNasdaq Capital Market.

Our stock price has been and continues to be volatile.

The market price for the Company'sour common stock could fluctuate due to various factors. In addition to other factors described in this section, these factors may include, among others:

conversion of outstanding stock options or warrants;

announcements by the Companyus or itsour competitors of new contracts, products, or technological innovations;investments;

developments in existing or new litigation;

changes in government regulations;

fluctuations in the Company'sour quarterly and annual operating results; and

general market and economic conditions.

In addition, the stock markets have, in recent years, experienced significant volume and price fluctuations. These fluctuations often have been unrelated to the operating performance of the specific companies whose stock is traded. Market prices and the trading volume of our stock may continue to experience significant fluctuations due to the matters described in this Item 1A,above, as well as economic and political conditions in the United States and worldwide, investors'investors’ attitudes towards our business prospects, and products, and changes in the interests of the investing community. As a result, the market price of the Company'sour common stock has been and may continue to be adversely affected and our shareholdersstockholders may not be able to sell their shares or to sell them at desired prices.

We may be subject to penny stock regulations and restrictions and you may have difficulty selling shares of our common stock.

The Company's programSEC has adopted regulations which generally define so-called “penny stocks” to repurchase itsbe an equity security that has a market price less than $5.00 per share or an exercise price of less than $5.00 per share, subject to certain exemptions. Our common stock is a “penny stock” and is subject to Rule 15g-9 under the Securities Exchange Act of 1934, as amended, or the Exchange Act. This rule imposes additional sales practice requirements on broker-dealers that sell such securities partiallyto persons other than established customers and “accredited investors” (generally, individuals with a net worth in relationexcess of $1 million or annual incomes exceeding $200,000 or $300,000 together with their spouses). For transactions covered by Rule 15g-9, a broker-dealer must make a special suitability determination for the purchaser and have received the purchaser’s written consent to short-sellingthe transaction prior to sale. As a result, this rule may affect the ability of itsbroker-dealers to sell our securities and may not have been successful into stemming such short-selling.

The Company embarked on a programaffect the ability of limited repurchasespurchasers to sell any of itsour securities in 2012the secondary market, thus possibly making it more difficult for us to raise additional capital.


For any transaction involving a penny stock, unless exempt, the rules require delivery, prior to any transaction in penny stock, of a disclosure schedule prepared by the SEC relating to the penny stock market. Disclosure is also required to be made about sales commissions payable to both the broker-dealer and 2013. Short-selling of its securities was believedthe registered representative and current quotations for the securities. Finally, monthly statements are required to have caused investors with a long-term interestbe sent disclosing recent price information for the penny stock held in the Company to demand thataccount and information on the company share their long-term view. The Company believed that the effects of its repurchase program would demonstrate the long-term view of its long-term investors. However, therelimited market in penny stock.

There can be no guaranteeassurance that the program was orour common stock will be regarded as successful. 

Shares eligiblequalify for future sale by the Company's current or future stockholders may cause the Company'sexemption from this rule. In any event, even if our common stock pricewere exempt from this rule, we would remain subject to decline.
If the Company's stockholders or holdersSection 15(b)(6) of the Company's other securities sell substantial amountsExchange Act, which gives the SEC the authority to restrict any person from participating in a distribution of penny stock, if the Company's common stockSEC finds that such a restriction would be in the public market, including shares issued in completed acquisitions or upon the exercise of outstanding options and warrants, then the market price of the Company's common stock could fall.
Issuance of shares of the Company's common stock upon the exercise of options or warrants will dilute the ownership interest of the Company's existing stockholders and could adversely affect the market price of the Company's common stock.
As of March 13, 2015, the Company had outstanding stock options to purchase an aggregate of 1,157,055 shares of common stock and warrants to purchase an aggregate of 1,381,179 shares of common stock. The exercise of the stock options and warrants and the sales of stock issuable pursuant to them would further reduce a stockholder's percentage voting and ownership interest. Further, the stock options and warrants are likely to be exercised when the Company's common stock is trading at a price that is higher than the exercise price of these options and warrants and the Company would be able to obtain a higher price for the Company's common stock than the Company would receive under such options and warrants. The exercise, or potential exercise, of these options and warrants could adversely affect the market price of the Company's common stock and the terms on which the Company could obtain additional financing. The ownership interest of the Company's existing stockholders may be further diluted through adjustments to certain outstanding warrants under the terms of their anti-dilution provisions.
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Securities analysts may not initiate coverage for the Company's common stock or may issue negative reports and this may have a negative impact on the market price of the Company's common stock.
The trading market for the Company's common stock may be affected in part by the research and reports that industry or financial analysts publish about the Company or the Company's business. It may be difficult for companies such as the Company, with smaller market capitalizations, to attract a sufficient number of securities analysts that will cover the Company's common stock. If one or more of the analysts who elect to cover the Company downgrades the Company's stock, the Company's stock price would likely decline rapidly. If one or more of these analysts ceases coverage of the Company, the Company could lose visibility in the market, which in turn could cause its stock price to decline. This could have a negative effect on the market price of the Company's stock.

Our management will have broad discretion over the use of the proceeds from the future sale of the securities.

In connection with the future sale of our securities, our management will have broad discretion to use the net proceeds from such sale, and investors will be relying on the judgment of our management regarding the application of such proceeds. Our management might not be able to yield a significant return, if any, on any investment of the net proceeds.
The Company has not paid dividends in the past and does not expect to pay dividends in the future.
The Company has never declared or paid cash dividends on its capital stock. The Company currently intends to retain all future earnings for the operation and expansion of its business and, therefore, does not anticipate declaring or paying cash dividends in the foreseeable future. The payment of dividends will be at the discretion of the Company's board of directors and will depend on the Company's results of operations, capital requirements, financial condition, prospects, contractual arrangements, any limitations on payments of dividends present in any of the Company's future debt agreements and other factors the Company's board of directors may deem relevant. If the Company does not pay dividends, a return on your investment will only occur if the Company's stock price appreciates.
The Company's future capital needs could result in dilution of your investment.
The Company's board

Our Board of directorsDirectors may determine from time to time that there is a need to obtain additional capital through the issuance of additional shares of the Company'sour common stock or other securities. These issuances would likely dilute the ownership interests of the Company'sour current investors and may dilute the net tangible book value per share of the Company'sour common stock. Investors in subsequent offerings may also have rights, preferences and privileges senior to the Company'sour current stockholders which may adversely impact the Company'sour current stockholders.

Our directors, executive officers

We have not paid dividends in the past and principal stockholdersdo not expect to pay dividends in the foreseeable future. 

We have never declared or paid cash dividends on our capital stock. We currently have substantial control over usintend to retain all future earnings for the operation and could delayexpansion of our business and, therefore, do not anticipate declaring or preventpaying cash dividends in the foreseeable future.

The payment of dividends will be at the discretion of our Board of Directors and will depend on our results of operations, capital requirements, financial condition, prospects, contractual arrangements, any limitations on payments of dividends present in any of our future debt agreements and other factors our Board of Directors may deem relevant. If we do not pay dividends, a change in corporate control.

As of March 13, 2015,return on your investment will only occur if our directors, executive officers and holders of more than 5% ofstock price appreciates.

Securities analysts may not initiate coverage for our common stock together with their affiliates, beneficially own, in the aggregate, approximately 46.3% of our outstanding common stock. Asor may issue negative reports and this may have a result, these stockholders, if they were to act together, could have significant influence over the outcome of matters submitted to our stockholders for approval, including the election of directors and any merger, consolidation or sale of all or substantially all of our assets. In addition, these stockholders, if they were to act together, could have significant influence over the management and affairs of our company. Accordingly, this concentration of ownership might harmnegative impact on the market price of our common stock.

The trading market for our common stock by:

delaying, deferring or preventing a change in corporate control;
impeding a merger, consolidation, takeover or other business combination involving us; or
discouraging a potential acquiror from making a tender offer or otherwise attempting to obtain control of us.

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may be affected in part by the research and reports that industry or financial analysts publish about us or our business. It may be difficult for companies such as us, with smaller market capitalizations, to attract a sufficient number of securities analysts that will cover our common stock. If one or more of the analysts who elect to cover our company downgrades our stock, our stock price would likely decline rapidly. If one or more of these analysts ceases coverage of our company, we could lose visibility in the market, which in turn could cause our stock price to decline. This could have a negative effect on the market price of our stock.

Nevada law and the Company'sour charter documents contain provisions that could delay or prevent actual and potential changes in control, even if they would benefit stockholders.

As of December 30, 2010, the Company became a corporation chartered in the State of Nevada. The Company is subject to provisions of the Nevada corporate statutes which prohibit a business combination between a corporation and an interested stockholder, which is generally a stockholder holding 10% or more of a company's stock.
The Company's

Our articles of incorporation authorize the issuance of preferred shares which may be issued with dividend, liquidation, voting and redemption rights senior to our common stock without prior approval by the stockholders. The preferred stock may be issued for such consideration as may be fixed from time to time by theour Board of Directors. TheOur Board of Directors may issue such shares of preferred stock in one or more series, with such designations, preferences and rights or qualifications, limitations or restrictions thereof as shall be stated in the resolution of resolutions.

The issuance of preferred stock could adversely affect the voting power and other rights of the holders of common stock. Preferred stock may be issued quickly with terms calculated to discourage, make more difficult, delay or prevent a change in control of the Companyour company or make removal of management more difficult. As a result, theour Board of Directors'Directors’ ability to issue preferred stock may discourage the potential hostile acquirer, possibly resulting in beneficial negotiations. Negotiating with an unfriendly acquirer may result in, among other things, terms more favorable to the Companyus and itsour stockholders. Conversely, the issuance of preferred stock may adversely affect any market price of, and the voting and other rights of the holders of the common stock. The Company presently has no plans to issue any preferred stock.


These and other provisions in the Nevada corporate statutes and our charter documents could delay or prevent actual and potential changes in control, even if they would benefit the Company's stockholders.

our stockholders

ITEM 1B.Item 1B.Unresolved Staff Comments
There are no unresolved comments from the staff of the Securities and Exchange Commission.
UNRESOLVED STAFF COMMENTS.

Not Applicable.

ItemITEM 2.PropertiesPROPERTIES.

We lease a 10,6725,581 sq. ft. facility in Horsham, Pennsylvania that houses our executive offices and marketing. The term of the lease runs through November 30, 2015. In addition, we lease a 7,140 sq. ft. facility in Orangeburg, New York that houses parts of sales and operations.finance. The term of the lease runs until September 30, 2016.

December 31, 2018. Monthly payments under this lease are approximately $6 thousand.

We lease office space at a 17,222 sq. ft. buildingfacility in Hod-Hasharon, Israel,Willow Grove, Pennsylvania that is used for marketing, operations and research and development.currently houses part of our legal department. The term of the lease runs untilexpired on April 30, 2017.

We2017 and we are now on a month-to-month lease. Monthly payments under this lease an 11,300 sq. ft. facility consistingare approximately $1 thousand.

Some of our executives occupy office manufacturing and warehousing space in Carlsbad, California. The lease expires on September 30, 2015. Our Carlsbad facility houses the manufacturing and development operations for our excimer laser business. We will begin negotiations to renew this lease within the next two months; we expect that this lease will be renewed without incident.

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Item 3.
Legal Proceedings
During the year ended December 31, 2013, Radiancy, Inc., a wholly-owned subsidiary of PhotoMedex, commenced legal action against Viatek Consumer Products Group, Inc., over Viatek's Pearl and Samba hair removal products which Radiancy believes infringe the intellectual property covering its no!no! hair removal devices. The first suit, which was filed in the United States Federal Court, Southern District of New York includes claims against Viatekthat is subject to an office service agreement between our CEO and another entity. Under the agreement, the fee is approximately $2 thousand per month. We intend to reimburse our CEO for patent infringement, trademarksuch costs.

In 2017, we acquired (i) three vacant land sites intended for development as gas stations in northern California, (ii) a 75% membership interest in a limited liability company that owns a vacant land site located in Northern California, in which profits and trade dress infringement,losses are allocated 75% to our company and false25% to the noncontrolling member subject to a preferred equity split in which the noncontrolling member earns the first 10% of net profits and misleading advertising. A second suit against Viatek was filedthe balance of the 90% is to be paid along the terms of the 75% split to our company and 25% to the noncontrolling member (iii) an interest in Canada, wherea limited liability company which owns property located in Los Lunas, New Mexico being developed as a single family residential development.

The proposed gas station sites are located in Atwater and Merced, California. We intend to explore our options for the Pearl is offered on that country's The Shopping Channel, alleging trademark and trade dress infringement, and false and misleading advertising. Viatek's response containsdevelopment of these properties. We may (i) lease a varietyproperty to a developer who will handle all further development of counterclaims and affirmative defenses against both Radiancy and its parentthe property, with our company PhotoMedex, including, among other counts, claims regarding the invalidity of Radiancy's patents and antitrust allegations regarding Radiancy's conduct.

Radiancy, and PhotoMedex, had moved to dismiss PhotoMedexreceiving monthly lease payments from the case,developer; (ii) engage a contractor to develop a property to a certain level, then lease it to a developer which will handle the final development and to dismissleasing of the counterclaims and affirmative defenses asserted by Viatek. On March 28, 2014, the Court granted the Company's motion and dismissed PhotoMedexproperty, with our company receiving monthly payments from the lawsuit.developer; or (iii) engage a contractor to completely develop a property, then lease it directly to a tenant who will remit monthly lease payments back to us. The Court also dismissed certain counterclaims and affirmative defenses asserted by Viatek, including Viatek's counterclaims against Radiancyoption or options selected for antitrust, unfair competition, and tortious interference with business relationships and Viatek's affirmative defensesthese properties will depend upon the types of unclean hands and inequitable conduct before the U.S. Patent and Trademark Officetenants interested in procuring its patent. Radiancy also moved for sanctions against Viatek for failure to provide meaningful and timely responses to Radiancy's discovery requests;operating gas stations and/or related ventures on April 1, 2014, the Court granted that motion. Viatek appealed both the sanctions ruling and the dismissal of Viatek's counterclaims and defenses from the case,those properties, as well as PhotoMedex's dismissal as a plaintiff;our capitalization and available financial resources. In these arrangements, the Court has denied those appeals. The Court has appointed a Special Masterconstruction and/or management of the properties are or will be handled by third-party firms which specialize in such work. Therefore, we anticipate that we will not need to oversee discovery. A Markman hearing on the patents at issue was held on March 2, 2015. Viatek has requested an opportunityhire significant additional personnel to supplement its patent invalidity contentions in the US case; Radiancy opposes that request. Radiancy has been granted permission by the US Court to supplement its earlier sanctions motion to include the legal feesdevelop, maintain and manage these properties. As for funding for any costs associated with preparingthese properties’ development, although we cannot provide any assurance that we will be able to obtain funding, we will seek funding from one or more of the following potential sources funding from third-party investors, funding as a result of loans secured by the properties, or joint-funding arrangements with developers and/or managers of these properties.

Below description of existing land and prosecuting that motion. As of December 31, 2014, discovery and related court hearings continuedevelopment assets upon contribution:

LocationStateStatusPercentage Interest Contributed
AtwaterCAExisting building on site, needs new plan submittal100.0%
AtwaterCAExisting building on site, needs new plan submittal100.0%
Merced CountyCAOriginal map approved, plan needs to be modified100.0%
Los Lunas(1)NMActive construction and sale property17.9%
Merced(2)CAUnder evaluation75.0%

(1) Based on percentage interest in both the US and the Canadian cases. At this time, the amount of any loss, or range of loss, cannot be reasonably estimated as the caseasset transferred by contributed entity. Refer to Item 1A. “Risk Factors.”

(2) Based on membership interest in contributed entity assigned to our company.


ITEM 3.LEGAL PROCEEDINGS.

JFURTI Litigation

Our company is still in the early stages of discoverya party to determine the validity of any claim or claims made by Viatek. Therefore, the Company has not recorded any reserve or contingent liability related to this particular legal matter. However, in the future, as the case progresses, the Company may be required to record a contingent liability or reserve for this matter. 

On December 20, 2013, PhotoMedex, Inc. was served with a class action lawsuitJFURTI, LLC, et al v. Suneet Singal, et al, filed in the United States District Court for the EasternSouthern District of Pennsylvania against the Company and its two top executives, Dolev Rafaeli,New York. The suit names as defendants Suneet Singal, an officer of various First Capital companies as well as our former Chief Executive Officer and Dennis M. McGrath, Presidentformer member of our Board of Directors, Frank Grant and Chief Financial Officer. Richard Leider, board members of First Capital Real Estate Investments, LLC, First Capital Real Estate Advisors, LP, Presidential Realty Corporation, Presidential Realty Operating Partnership, Downey Brand LLP, and now our company (under its previous name, PhotoMedex Inc.), as well as nominal derivative defendants the Contributor and the Contributor Parent. Mr. Leider is also on the Board of Directors of our company.

The suit is the ninth filed by Jacob Frydman and/or JFURTI, LLC in a dispute between the plaintiffs and the First Capital group of companies, which entered into a series of agreements with Mr. Frydman beginning in September 2015. Mr. Frydman had founded, sponsored, and taken public United Realty Trust Incorporated, a Real Estate Investment Trust, or the REIT. Mr. Frydman was the CEO and Chairman of the REIT as well as the owner of various other United Realty branded companies affiliated with the REIT business. In September 2015, Mr. Frydman and Mr. Singal negotiated and agreed to a transaction between various First Capital branded companies, on the one hand, and the United Realty branded companies affiliated with the REIT business, on the other hand, as a result of which the REIT was rebranded as the Contributor Parent.

After the September 2015 transaction was concluded, several disputes arose between the parties. This suit is the ninth action brought by Mr. Frydman in state and federal courts relating to these disputes, and the second attempt by Mr. Frydman and JFURTI to bring federal claims derivatively in this Court against First Capital entities and other parties. The first action, titled JFURTI, LLC and Jacob Frydman v. Forum Partners Investment Management LLC et al., No. 16 Civ. 8633 or the Prior Action, commenced on November 7, 2016 and asserted, inter alia, derivative RICO and securities fraud claims. The Court dismissed the action in a decision and order dated April 27, 2017.

Following dismissal of the Prior Action, Mr. Frydman sent letters to each member of the Contributor Parent’s Board of Directors, or the Demand Letter, demanding that the Board investigate and remediate the dissipation of assets as alleged by plaintiffs. In particular, the Demand Letter questioned (i) a letter of intent with Presidential Realty Corporation, or Presidential, announced in an 8-K filed by the Contributor Parent on or about July 18, 2016; (ii) the Contributor Parent’s use of funds raised between September 15, 2015 and February 28, 2016; (iii) an interest contribution agreement with Presidential entered into on or about December 16, 2016; (iv) the Contributor Parent’s failure to file quarterly and annual reports; (iv) an interest contribution agreement entered into on March 31, 2017 with our company; and (v) other purportedly fraudulent acts such as publishing an artificially inflated net asset value, defaulting on certain mortgage loans, misrepresentations by Mr. Singal with respect to certain properties contributed to the Contributor Parent through the Master Agreement executed on September 15, 2015, and various loan agreements with Forum Partners Investment Management LLC, or Forum. The Demand Letter also demanded inspection of certain corporate documents pursuant to Md. Code § 2-512.

The Contributor Parent commenced such an investigation, and offered such an inspection, but Mr. Frydman and JFURTI failed to wait for the results of the investigation or make any inspection, and instead brought suit in the same court as the Prior Action. The suit alleges, among other claims, violations of the Federal securities laws between November 7, 2012 and November 14, 2013. A mediation on possible settlement of this action was held on November 10, 2014; the parties including the Company's insurance carrier have agreed on a possible settlement. The Company has paid its own legal fees up to the deductible cap on its insurance policy, and all amounts to be paid to plaintiffs and plaintiff's counsel will be paid by the carrier§ 10(b) of the insurance policy. This settlement is subject to reviewExchange Act and approval by the District Court, which has not yet rendered its opinion.

The Company was served on July 29, 2014 with an application to certify a class action, filed in Israel District CourtRule 10b-5 (1) against Mr. Singal and First Capital Real Estate Investments LLC for Tel Aviv against the Company and its two top executives, Dolev Rafaeli, Chief Executive Officer, and Dennis M. McGrath, President and Chief Financial Officer. The plaintiff's who initiated this complaint have agreed to be part of, and be bound by, the possible settlement reached in the United States District Court for the Eastern District of Pennsylvania against the Company and the same two top executives.
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There were multiple class-action lawsuits filedmisrepresentations in connection with PhotoMedex's proposed acquisition of LCA-Vision, Inc. All cases asserted claimsthe Master Agreement entered into on September 15, 2015 and related agreements; (2) against LCA-Vision, Inc.Downey Brand for failure to file certain deeds; (3) against First Capital defendants (except Grant and Leider), Forum defendants, and Presidential defendants for a mix of otherfraudulent scheme to sell Contributor Parent assets to Presidential; and (4) against First Capital defendants, including LCA's chief executive officerForum defendants, and directors, PhotoMedex, and Gatorade Acquisition Corp., a wholly owned subsidiary of PhotoMedex. The complaints generally allege thatour company for the proposed acquisition undervalued LCA and deprived LCA's shareholderstransfer of the opportunityContributor Parent and Contributor assets to participateus in LCA's long-term financial prospects, that the "go shop"exchange for allegedly worthless shares. There are also claims under state law for common law fraud, conversion, fraudulent conveyance, waste and "deal-protection" provisionsmismanagement, accounting, injunctive relief, and violation of Cal. Bus. & Prof. Code § 17-200. Many of the Merger Agreementclaims asserted in the complaint, including the securities fraud claims, were designednever raised in the Demand Letter, as required by law. The suit seeks damages against all defendants for the failure of the Contributor Parent to prevent LCA from soliciting or receiving competing offers, that LCA's Board breached its fiduciary dutiesrespond to the Demand Letter, and failedan injunction against the sale of the assets to maximize that company's stockholder value, and that LCA, PhotoMedex, and Gatorade aided and abetted the LCA defendants' alleged breaches of duty. Presidential defendants.


The parties have reachedsubmitted a possible settlementmotion for an order (i) staying all proceedings in these suits,this action for 60 days, or until the end of 2017, and (ii) extending the defendants time to respond to the complaint, or to make a motion with respect to the complaint, until 45 days after the Contributor Parent’s response to the Demand Letter. The Court granted that motion on October 31, 2017. Upon completion of their investigation, the Contributor Parent provided a response to the Demand Letter, denying all claims made in the letter. A Motion to Dismiss this action has now been filed with the Company contributing less than $100,000Court on behalf of all plaintiffs.

Our company intends to the settlement, plus the payment of its legal fees, and the remainder of the settlement being covered by the insurance carriers.  This settlement is subject to review and approval by the state court, which has not yet rendered its opinion.

On April 25, 2014, a class action lawsuit was filed in the United States District Court for the District of Columbia against the Company's subsidiary, Radiancy, Inc. and Dolev Rafaeli, Radiancy's President. The suit was filed by Jan Mouzon and twelve other customers residing in ten different states who purchased Radiancy's no!no! Hair products. It alleges various violations of state business and consumer protection codes including false and misleading advertising, unfair trade practices, and breach of express and implied warranties. The complaint seeks certification of the putative class, or, alternatively, certification as subclasses of plaintiffs residing in those specific states. The complaint also seeks an unspecified amount of monetary damages, pre-and post-judgment interest and attorneys' fees, expert witness fees and other costs. Dr. Rafaeli was served with the Complaint on May 5, 2014; to date, Radiancy, has not been served. The Company has filed a motion to dismiss this case; that motion is pending before the Court. A mediation was scheduled in this matter for November 24, 2014, but no settlement was reached. Radiancy and its officers intend todefend itself vigorously defend themselves against this lawsuit.suit. At this time, the amount of any loss, or range of loss, cannot be reasonably estimated as the case has only been initiated and no discovery has been conducted to determine the validity of any claim or claims made by plaintiffs. Therefore, the Company haswe have not recorded any reserve or contingent liability related to these particular legal matters. However, in the future, as the cases progress, the Companywe may be required to record a contingent liability or reserve for these matters.
On June 30, 2014,

Linda Andrews Litigation

During 2016, Linda Andrews, an alleged user of the Company'sno!no! Hair device, filed a product liability claim against our company, its subsidiary Radiancy, Inc., was served with a class action lawsuit filedand Dr. Dolev Rafaeli, in the SuperiorUnited States District Court for the Middle District of Florida, Orlando Division, alleging that use of the device had caused a relapse of and complication to a pre-existing medical condition resulting from her treatment for cancer.  The complaint alleged, among other claims, that Radiancy failed to provide adequate warnings regarding the operation of the device.  We and Dr. Rafaeli filed a motion to dismiss the claims against them and Radiancy filed an answer to the Complaint.  Ms. Andrews then sought leave to amend her complaint to clarify the claims. Our company, Radiancy and Dr. Rafaeli filed appropriate responses and renewed the motion to dismiss the claims against our company and Dr. Rafaeli.

On June 22, 2017, the United States District Court for the Middle District of Florida, Orlando Division, dismissed the claims against our company and Dr. Dolev Rafaeli without prejudice. Radiancy remained a defendant in the State of California, County of Kern.suit.

Radiancy entered into a settlement with Ms. Andrews in 2017. The suit was filed by April Cantley, who purchased Radiancy's no!no! Hair products. It alleges various violations of state business and consumer protection codes including false and misleading advertising, breach of express and implied warranties and breachterms of the California Legal Remedies Act. The complaint seeks certification of the class,settlement are confidential.

Other Litigation

Our company and certain subsidiaries are involved in other miscellaneous litigation and legal actions, including product liability, consumer, commercial, tax and governmental matters, which consists of customers in the State of California who purchased the no!no! Hair devices. The complaint also seeks an unspecified amount of monetary damages, pre-and post-judgment interest and attorneys' fees, expert witness fees and other costs. Radiancy has filed an Answer to this Complaint; the case is now in the discovery phase. Radiancy and its officers intend to vigorously defend themselves against this lawsuit. Discovery has now commenced in this action. At this time, the amount of any loss, or range of loss, cannot be reasonably estimated as the case has only been initiated and no discovery has been conducted to determine the validity of any claim or claims made by plaintiffs. Therefore, the Company has not recorded any reserve or contingent liability related to these particular legal matters. However, in the future, as the cases progress, the Company may be required to record a contingent liability or reserve for these matters.

Fromcan arise from time to time in the ordinary course of our business, we and certain of our subsidiaries are involved in certain other legal actions and claims, including product liability, consumer, commercial, tax and governmental matters, and claims regarding false advertising and product efficacy against the no!no! Hair products which were already raised and reviewed in the Tria litigation.business. We believe based on discussions with legal counsel, that these other litigations and claims will likely be resolved without a material effect on our consolidated financial position, results of operations or liquidity. However, litigation isand legal actions are inherently unpredictable, and excessive verdicts can result from litigation.in such situations. Although we believe that we have or will have substantial defenses in these matters, weit may, in the future, incur judgments or enter into settlements of claims that could have a material adverse effect on our results of operations in a particular period.
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ItemITEM 4.Mine Safety DisclosuresMINE SAFETY DISCLOSURES.
None.

Not applicable.

PART II

ItemITEM 5.Market for Registrant's Common Equity, Related Stockholder Matters and Issuer Purchases of Equity SecuritiesMARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES.
As of March 13, 2015, we had 22,101,718 shares of common stock issued and outstanding, including 2,166,663 shares of issued and outstanding restricted stock. This did not include (i) options to purchase 1,157,055 shares of common stock, of which 557,188 were vested as of March 13, 2015, or (ii) warrants to purchase up to 1,381,179 shares of common stock, all of which warrants were vested.

Market Information

Our common stock is listed on the Nasdaq Global SelectCapital Market ("Nasdaq") under the symbol "PHMD."“FCRE” (formerly “PHMD”). The following table sets forth, for the periods indicated, the high and low closing sale prices per share of our common stock:

 HighLow
Year Ended December 31, 2014:  
Fourth Quarter$5.97$1.05
Third Quarter12.616.20
Second Quarter15.7311.81
First Quarter16.8013.00
Year Ended December 31, 2013:  
Fourth Quarter$15.86$11.53
Third Quarter16.5914.62
Second Quarter16.9514.71
First Quarter16.4713.95
On March 13, 2015,stock. This table has been updated to reflect the last reported sale price for our commonreserve stock on Nasdaq was split effected September 23, 2016.


  High  Low 
Year Ended December 31, 2017:        
Fourth Quarter $1.46  $0.82 
Third Quarter  1.27   0.71 
Second Quarter  1.77   1.12 
First Quarter  2.64   1.73 
Year Ended December 31, 2016:        
Fourth Quarter $4.78  $1.03 
Third Quarter  6.50   1.10 
Second Quarter  2.65   1.05 
First Quarter  3.05   1.85 

$1.70Approximate Number of Holders of Our Common Stockper share.

As of March 13, 2015,30, 2018, we had approximately 642 1,095 stockholders of record, without giving effect to determining the number of stockholders who held shares in "street name"“street name” or other nominee accounts.

Dividend Policy

We have not declared or paid any dividend on our common stock, since our inception. We do not anticipate that any dividends on our common stock will be declared or paid in the foreseeable future. Under the terms of the Second Amended and Restated Forbearance Agreement dated February 28, 2015, we may not declare or pay dividends on our common stock.

66

Overview of

Securities Authorized for Issuance under Equity Compensation Plans

The following is a summary

See Item 12 “Security Ownership of allCertain Beneficial Owners and Management and Related Stockholder Matters.”

Recent Sales of ourUnregistered Securities

We have not sold any equity compensation plans, including planssecurities during the 2017 fiscal year that were assumed through acquisitions and individual arrangementsnot previously disclosed in a quarterly report on Form 10-Q or a current report on Form 8-K that provide forwas filed during the issuance of equity securities as compensation, as of December 31, 2014. See Notes 1 and 12 to the consolidated financial statements for additional discussion.

 EQUITY COMPENSATION PLAN INFORMATION
 
 
Number of Securities to be Issued Upon Exercise of Outstanding Options, Warrants and Rights
 
 
Weighted-Average Exercise Price of Outstanding Options, Warrants and Rights
 
 
Number of Securities Remaining Available for Future Issuance Under Equity Compensation Plans (excluding securities reflected in
column (A))
 (A) (B) (C)
Equity compensation plans     
approved by security holders2,540,733 $15.99 3,465,202
      
 Equity compensation plans not approved by security holders---
      
Total2,540,733 $15.99 3,465,202
Options have been granted to employees and/or consultants out of our 2005 Equity Compensation Plan. Options to our outside directors will be made from our 2000 Non-Employee Director Stock Option Plan. Most warrants issued by us have been to investors or placement agents, and no warrants have been issued pursuant to equity compensation plans. Additionally, all outstanding options were granted as compensation for benefits inuring to us other than for benefits from capital-raising activities. With limited exceptions under Nasdaq membership requirements, we intend in the future to issue options pursuant to equity compensation plans which have already been approved by our stockholders.
Recent Issuances of Unregistered Securities
None.
Recent Issuances of Unregistered Securities
None.
2017 fiscal year.

Purchases of Equity Securities

None.
67


No repurchases of our common stock were made during the fourth quarter of 2017.

ItemITEM 6.Selected Financial DataSELECTED FINANCIAL DATA.
You should read the following selected historical consolidated financial data in conjunction with our consolidated financial statements included elsewhere in this Report and "Management's Discussion and Analysis of Financial Condition and Results of Operations" beginning in Item 7 below. The selected historical consolidated statements of operations data for the years ended December 31, 2014, December 31, 2013 and December 31, 2012, and the selected historical consolidated balance sheet data as of December 31, 2014 and December 31, 2013, are derived from our audited consolidated financial statements included in this Report. The selected historical consolidated statements of operations data for the years ended December 31, 2011 and December 31, 2010 and the selected historical consolidated balance sheet data as of December 31, 2011, December 31, 2010 and December 31, 2009 are derived from our audited consolidated financial statements not included in this Report. The historical results presented here are not necessarily indicative of future results. As the merger with Radiancy Inc. in December 2011 was considered to be a reverse merger, the results of the operations of Pre-merged PhotoMedex are not included in the Statements of Operations prior to the reverse merger on December 13, 2011. The financial position of the Company reflects the completion of the reverse acquisition in the Balance Sheets except the Balance Sheet at December 31, 2010.
  Year Ended December 31, 
  (In thousands, except per-share data) 
  2014  2013  2012  2011  2010 
Statement of Operations Data:          
Revenues $163,541  $224,664  $220,651  $132,082  $70,071 
Costs of revenues  38,619   45,035   46,642   26,296   16,465 
  Gross profit  124,922   179,629   174,009   105,786   53,606 
Selling, general and administrative  142,880   154,278   143,817   107,377   34,596 
Engineering and product development  3,086   3,306   2,914   1,057   839 
  Income (loss) from continuing operations before financing income (expense) and interest  (21,044)  
22,045
   
27,278
   (2,648)  
18,171
 
Interest and other financing income (expenses), net  (4,387)  702   (351)  (68)  (283)
  Income (loss) from continuing operations before tax expense (benefit)  (25,431)  22,747   26,927   (2,716)  17,888 
Income tax (expense) benefit  (36,312)  (4,370)  (4,438)  2,022   (6,287)
Income (loss) from continuing operations (61,743) $18,377  $22,489  (694) $11,601 
Discontinued operations:                    
  Loss from discontinued operations  (15,155)  -   -   -   - 
  Estimated loss on sale of discontinued operations  (44,598)  -   -   -   - 
Net income (loss) (121,496) $18,377  $22,489  (694) $11,601 
                     
Basic net income (loss) per  share:                    
  Continuing operations (3.25) $0.90  $1.10  (0.06) $1.13 
  Discontinued operations (3.16) $0.00  $0.00  $0.00  $0.00 
Basic net income (loss) per share (6.41) $0.90  $1.10  (0.06) $1.13 
                     
Diluted net income (loss) per  share:                    
  Continuing operations (3.25) $0.89  $1.08  (0.06) $0.99 
  Discontinued operations (3.16) $0.00  $0.00  $0.00  $0.00 
Diluted net income (loss) per share (6.41) $0.89  $1.08  (0.06) $0.99 
Shares used in computing net income (loss) per share                    
  Basic  18,940   20,455   20,356   11,602   10,256 
  Diluted  18,940   20,657   20,764   11,602   11,725 
Balance Sheet Data (At Period End):                    
Cash and cash equivalents and short-term deposits $10,692  $59,501  $62,348  $16,549  $22,081 
Working capital  25,537   83,058   95,677   30,768   27,511 
Total assets  187,763   220,108   211,890   144,331   46,387 
Long-term debt (net of current portion)  37,793   82   -   8   - 
Other long-term liabilities  1,229   3,640   4,067   2,405   837 
Stockholders' equity $42,265  $160,361  $167,327  $110,725  $28,900 
68

Not applicable.

ItemITEM 7.Management's Discussion and Analysis of Financial Condition and Results of OperationsMANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS.

The following financial data, in this narrative, are expressed in thousands, except for the earnings per share. The following management’s discussion and analysis should be read in conjunction with our financial statements and the Consolidated Financial Statementsnotes thereto and related notes includedthe other financial information appearing elsewhere in this Report.

Introduction, Outlookreport.

Overview

Our company, founded in 1980, is transitioning from its former business as a skin health company to a real estate development and Overviewasset management company, concentrating primarily on investments in high quality income producing assets, hotel and resort developments, residential developments and other opportunistic commercial properties.

Until the recent sale of Businessour consumer products division, we were a global skin health company providing integrated disease management and aesthetic solutions to dermatologists, professional aestheticians and consumers. Starting in 2014, we began to sell off certain business units and product lines and on January 23, 2017, we sold the last remaining major product line, our consumer products division, (see Note 2 Discontinued Operations, to our consolidated financial statements). Following this transaction, we had only minimal operations and assets remaining of immaterial value to our company. We are in the process of selling those assets, remaining inventory and assets of this business line, after which time we will no longer operate within the skin health business.


As a result of the Contribution Transaction described below, we became a real estate development and asset management company. Our current strategic focus is built upon three key components:

Skilled direct sales force to target Physician and Professional Segments;
Expertise in global consumer marketing;
A full product life cycle model representing the ability to develop and commercialize innovative products from concept through regulatory and physician acceptance, and ultimately marketed directly to the consumer as dictated by normal product life-cycle evolution; and
to build our company into a leading real estate, asset management and development company concentrated primarily on investments in high yield income producing assets and other opportunistic commercial properties via direct property ownership and asset management. Our objective is to generate long term net asset value growth while adhering to institutional best practices and a deep research process for all investments.

For income producing properties, we intend to acquire assets that provide recurring income with the potential for income growth over the long-term. We believe there can be an attractive risk/reward profile to such properties based on the location and the underlying creditworthiness of the tenants. We intend to use such income generation to fund additional acquisitions and development opportunities and general corporate purposes. In addition, we intend to invest in land assets that can be developed into income generating properties. We believe that our size and scale provide an opportunity to take advantage of smaller-tier assets that most traditional investors do not focus on due to size limitations, thus creating unique investment opportunities. In particular, we intend to target assets in secondary and tertiary markets with assets that require minimal capital expenditures but generate initial unlevered cash flow yields that are one of only a few aesthetic companies to have developed professional technologies geared toward physicians and med spas and adapting them for the home-use market and have successfully sold millions of these products to consumers. Our professional- and consumer-use products are listed below, noting that this is not an exhaustive listinghigher than those in primary markets.

A second component of our product portfolio but represents our current key areasinvestment strategy will revolve around sourcing asset management opportunities for which we would operate as an asset manager of focus.

Key Technology Platforms
Thermicon® brand Heat Transfer Technology. In this technique, a patented thermodynamic wire gently singes and burns off the hair above the skin's surface. It conducts heat pulses, which enables longer-lasting hair removal. This technology drives our home-use no!no! Hair Removal 8800™ device, which is designed to reduce hair growth. Product variations include devices designed for men and for sensitive, small areas such as the face, among other versions including the recently launched no!no! Hair Removal PRO which introduces patented pulsed Thermicon technology producing 35% more energy aimed at removing more hair in less time.
LHE® brand Technology. LHE® combines direct heat and a full-spectrum light source to give a greater treatment advantage for psoriasis and acne care, skin tightening, skin rejuvenation, wrinkle reduction, collagen renewal, vascular and pigmented lesion treatments, and hair removal. Using LHE®, the Mistral intelligent phototherapy medical device can treat a larger spot size than a laser with less discomfort. In addition, our research finds that LHE offers meaningful results for thin, light hair. The technology is used in the no!no! Skin™, a handheld consumer product sold worldwide under the no!no!® brand. The no!no! Skin™ is a 510(k)-cleared product that has been clinically shown to reduce acne by 81% over 24 hours. The technology is also used in the no!no! Glow™, which is a 510(k)-cleared device and is a miniaturized LHE device also delivering ant-aging benefits for the at-home consumer in a hand-held size.
Kyrobak®. Kyrobak uses clinically proven, proprietary technology to treat unspecified, lower back pain. The unique combination of Continuous Passive Motion (CPM) and Oscillation therapy is a non-invasive, relaxing method for long lasting relief of back pain. Used for better than 3 decades in professional rehabilitation and chiropractic settings, CPM has been proven to increase mobility of the joints, draw more oxygen and blood flow to the area, allowing the muscles to relax and release pressure between the vertebrae allowing the spine to open up and decompress.
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XTRAC® Excimer Laser. XTRAC received an FDA clearance in 2000 and has since become a widely recognized treatment among dermatologists for psoriasis and other skin conditions for which there are no cures. The machine delivers narrow ultraviolet B ("UVB") light to affected areas of skin, leading to psoriasis remission in an average of 8 to 12 treatments and of vitiligo after 48 treatments. XTRAC is endorsed by the National Psoriasis Foundation, and its use for psoriasis is covered by nearly all major insurance companies, including Medicare. More than half of all major insurance companies now offer reimbursement for vitiligo as well, a figure that is increasing.
NEOVA®. This line of topical formulations is designed to prevent premature skin aging due to UV-induced DNA damage. The therapy seeks to repair photo-damaged skin using a novel combination of two key ingredients: DNA repair enzymes and our Copper Peptide Complex®. The NEOVA line includes DNA Damage Control SILC SHEER SPF 45, an award-winning tinted sunscreen. The DNA repair enzymes of this sunscreen are clinically shown to reduce UV damage by 45% and increase UV protection by 300% in one hour.
Light-emitting Diode (LED) Technology. PhotoMedex's LED technology is used in both its Omnilux™ and Lumière Light Therapy systems. Omnilux is FDA cleared to treat wrinkles, acne, minor muscle pain and pigmented lesions, and is applicable to all skin types. Lumière is designed for use in non-medical applications and combines the LED light with a line of topical lotions to improve the appearance of fine lines, wrinkles, skin tone and blemishes, giving aesthetic professionals a complete non-invasive skin care solution.
Our revenue generation is categorizedreal estate properties. We are not structured as Consumer, Physician Recurring or Professional. Each of our segments benefit from the combination of our proprietary global consumer marketing engine with our direct sales force for U.S. physicians, and are described below.
Consumer
The global consumer market is our largest business unit due to our success at bringing professional technologies into the home-use arena. Cumulatively,a REIT, thus we have sold more than 5 million no!no!® products to consumers, the majority of whom have been in Japan and North America.
We continue to develop and add to our marketing programs (in types of creative, languages, and media formats – print, online, radio, and TV) to effectively reach the large population groups where we have expanded our sales efforts, including: the United States with approximately 318 million people; Japan with a population of approximately 127 million people; Brazil (pop.187 million); Germany (pop. 81 million); United Kingdom (pop. 64 million); Columbia (pop. 47 million); Canada (pop. 35 million); Australia (pop. 23 million) and Hong Kong (pop. 7 million).
Our consumer marketing platform is built upon a proprietary direct-to-consumer sales engine and creative marketing programs that drive brand awareness. It is highly dependent upon the ability to procure cost effective advertising media to reach our targeted customer, particularly short-form TV advertising.
Sales Channels
Our multi-channel marketing and distribution model consists of television, online, print and radio direct-response advertising, as well as high-end retailers. We believe that this marketing and distribution model, through which each channel complements and supports the others, provides:
greater brand awareness across channels;
cost-effective consumer acquisition and education;
premium brand building; and
improved convenience for consumers.
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Direct to Consumer. Our direct-to-consumer channel consists of sales generated through commercials, infomercials, websites and call centers. We utilize several forms of advertising to drive our direct-to-consumer sales and brand awareness, including print, online, television and radio.
Retailers and Home Shopping Channels. Our retailers and home shopping channels enable us to provide additional points of contact to educate consumers about our solutions, expand our presence beyond our direct to consumer activity and further strengthen and enhance our brand image.
Distributors. In some territories, we operate through exclusive distribution agreements with leading distribution companies that are dominant in their respective market and have the ability to promoteretain all earnings and to operate in real estate asset management, development and peripheral real estate activities, items limited by REIT requirements. We will look to utilize our existing infrastructure to provide economies of scale to owners of real estate assets as it grows its portfolio over time.

Recent Developments

Contribution Agreement

On March 31, 2017, we entered into the Contribution Agreement with the Acquiror and the Contributor Parties, which was amended on August 3, 2017, October 11, 2017 and December 22, 2017. Pursuant to the Interest Contribution Agreement, as amended, the Contributor transferred $10 million of assets to the Acquiror, consisting of the following: (i) three vacant land sites intended for development as gas stations located in northern California, a 75% interest in a limited liability company that owns a vacant land site intended for development as a gas station, located in northern California; and (iii) a 100% interest in a limited liability company, which we refer to as the Avalon Interest, which owns a 17.9133% interest in a limited liability company called Avalon Jubilee LLC that owns property located in Los Lunas, New Mexico being developed as a single family residential development.

In exchange for these assets, we issued to the Contributor 879,234 shares of our common stock, which represented approximately 19.9% of our issued and outstanding common stock immediately prior to the Closing Date, at a per share value of $2.5183, or approximately $2.2 million in the aggregate. We issued the remaining $7.8 million of the approximately $10 million consideration to the Contributor in the form of 123,668 shares of our newly designated non-voting Series A Convertible Preferred Stock. Each share of the Series A Convertible Preferred Stock is convertible into 25 shares of our common stock, subject to the satisfaction of certain conditions, including stockholder approval of such conversion.

We elected to early adopt ASU 2017-01,Business Combinations (Topic 805) Clarifying the Definition of a Business.Accordingly, the determination of whether the transaction represents a business combination was evaluated by applying ASU 2017-01 guidance. We have determined that the group of assets assumed do not include (and also, none of them on a stand-alone basis) include, an input and a substantive process that together significantly contribute to the ability to create output and thus it was determined that the contribution represents an acquisition of assets rather than a business combination. Accordingly, the total sum of the fair value of consideration given (i.e. the fair value of the equity interests issued) together with the transaction costs, was allocated to the individual assets acquired and liabilities assumed based on their relative fair values at the date of acquisition. Such allocation did not give rise to goodwill.

See Item 1 “Business—Recent Developments—Contribution Transaction” for more information.

Payout Notes and Stock Grant Agreement

Under the Contribution Agreement, amounts due to Dr. Dolev Rafaeli and Dennis M. McGrath under their employment agreements, as well as amounts due to Dr. Yoav Ben-Dror for his services as a board member and officer of our foreign subsidiaries, were converted to convertible secured notes in the principal amounts of approximately $3.1 million, $0.98 million and $1.5 million, respectively, following approval from our stockholders on October 12, 2017 (which we refer to as the Payout Notes). The Payout Notes were due on October 12, 2018, carried a ten percent (10%) interest rate, payable monthly in arrears commencing on December 1, 2017, and were secured by a security interest in all of our assets pursuant to a security agreement that we entered into with the holders of the Payout Notes on October 12, 2017.


On December 22, 2017, we entered into the Stock Grant Agreement, with Dr. Dolev Rafaeli, Dennis M. McGrath and Dr. Yoav Ben-Dror (collectively referred to herein as the Note Holders) to (i) cause the early conversion of the Payout Notes into an aggregate of 5,628,291 shares of our common stock (which we refer to as the Payout Shares), (ii) effectuate the release of all security interests associated with the Payout Notes, (iii) provide for the issuance of an aggregate of 1,857,336 additional shares of common stock to the Note Holders as consideration for the various agreements of the Note Holders contained in the Stock Grant Agreement (which we refer to as the Additional Shares), (iv) provide for certain cash payments to the Note Holders in amounts equal to the interest payments that would have been made to the Note Holders absent the conversion of the Payout Notes, (v) obtain the agreement of the Note Holders to provide certain support services to our company, and (vi) obtain the conditional resignation of certain of the Note Holders from our Board of Directors. Accordingly, the Payout Notes were paid in full.

Pursuant to the Stock Grant Agreement, we agreed to make twelve (12) monthly payments on the first of each month commencing on January 1, 2018 of approximately $21, $7 and $10 thousand respectively, to Messrs. Rafaeli, McGrath, and Ben-Dror, respectively (which we refer to as the Cash Payments). The Cash Payments are consideration for certain consulting services provided by the Note Holders specified in the Stock Grant Agreement.

See Item 1 “Business—Recent Developments—Payout Notes and Stock Grant Agreement” for more information.

Private Placement

On December 22, 2017, we entered into the Purchase Agreement with OFI, under which OFI may invest up to $15 million in our company in a series of closings, in exchange for which OFI will receive shares of our newly designated Series B Preferred Stock at a purchase price of $1.00 per share.

On December 22, 2017, we completed the first closing under the Purchase Agreement, pursuant to which OFI provided $1.5 million to us in exchange for 1,500,000 shares of Series B Preferred Stock. On January 24, 2018, we completed a second closing under the Purchase Agreement, pursuant to which OFI provided approximately $2.2 million to us in exchange for 2,225,000 shares of Series B Preferred Stock. Under the Purchase Agreement, OFI may, but is not obligated to, make additional investments in one or more subsequent closings until an aggregate amount of $15 million has been invested or the Purchase Agreement has been terminated in accordance with its terms.

Under the Purchase Agreement, the proceeds from the first closing were to be used for working capital and general corporate purposes, the proceeds from the second closing were to be used to perform due diligence and invest in Income Generating Properties (as defined in the Purchase Agreement) that have been approved by our company’s Board of Directors, and proceeds from subsequent closings were be used to invest in Income Generating Properties (as defined in the Purchase Agreement) that have been approved by our Board of Directors or as otherwise agreed to between us and OFI in writing prior to such subsequent closings. On March 16, 2018, we and OFI entered into a letter agreement, pursuant to which OFI agreed that we may use all proceeds for the purposes and uses described in a budget agreed to between us and OFI at the time the letter agreement was signed. In connection with such letter agreement, we agreed to provide OFI, on a quarterly basis, on or prior to 15 days after the end of each quarter, a report that describes, in reasonable detail, the actual expenses incurred, and payments made during such period compared to the expenses and payments specified in the budget for such period, certified by our Chief Financial Officer.

The Purchase Agreement may be terminated by the written agreement of us and OFI, or by us or OFI if the final closing does not take place prior to December 31, 2018.

See Item 1 “Business—Recent Developments—Private Placement” for more information.

Going Concern

The accompanying financial statements have been prepared assuming we will continue as a going concern, which contemplates the realization of assets and satisfaction of liabilities in the normal course of business.


As of December 31, 2017, we had an accumulated deficit of approximately $134.45 million and shareholders’ deficit of approximately $2.9 million. To date, and subsequent to the recent sale of our last significant business unit, we have dedicated most of our financial resources to general and administrative expenses. At present, we are only generating de minimis income from our legacy operating activities.

Cash and cash equivalents as of December 31, 2017 were approximately $0.95 million. We have historically financed our activities with cash from operations, the private placement of equity and debt securities, borrowings under lines of credit and, in the most recent periods with the sale of certain assets and business units.

On March 31, 2017, we entered into the Contribution Agreement, under which certain real estate investment properties were contributed to our company in exchange for the issuance of our capital stock. Closing of the Contribution Agreement occurred on May 17, 2017. However, the assets assumed in such contribution do not represent a business and are not producing cash flows and/or revenues.

On December 22, 2017, we entered into the Purchase Agreement with OFI, under which OFI may invest up to $15 million in our company in a series of closings, in exchange for which OFI will receive shares of our newly designated Series B Preferred Stock at a purchase price of $1.00 per share. On December 22, 2017, we completed the first closing under the Purchase Agreement, pursuant to which OFI provided $1.5 million to us. On January 24, 2018, we completed a second closing under the Purchase Agreement, pursuant to which OFI provided approximately $2.2 million to us in. Under the Purchase Agreement, OFI may, but is not obligated to, make additional investments in one or more subsequent closings until an aggregate amount of $15 million has been invested or the Purchase Agreement has been terminated in accordance with its terms. OFI has no obligation to continue to invest in our company, and there are restrictions placed by OFI on the use of these funds.

We will be required to obtain additional liquidity resources in order to support our operations. We are addressing our liquidity needs by seeking additional funding from lenders and investors. There are no assurances, however, that we will be able to obtain an adequate level of financial resources required for the short and long-term support of our operations.

These conditions raise substantial doubt about our ability to continue as a going concern. The accompanying consolidated financial statements do not include any adjustments to reflect the possible future effects on recoverability and classification of liabilities that may result from the outcome of this uncertainty.

Reportable Segments

Before we commenced our current real estate business, we organized our business into three operating segments based upon our management structure, products through their existing retail and home shopping networks.

Markets
North America. Ourservices offered, markets served and types of customers, as follows: The Consumer segment (sold to ICTV on January 23, 2017, see Note 2 Discontinued Operations, to our consolidated financial statements) derived its revenues from the design, development, manufacturing and selling of long-term hair reduction and acne consumer distributionproducts. The Physician Recurring segment in North America hadderived its revenues from the XTRAC (sold to MELA Sciences on June 22, 2015) procedures performed by dermatologists, the sales of approximately $90.6 million, $147.7 millionskincare products (sold to Pharma Cosmetics on September 15, 2016), the sales of surgical disposables and $141.5 million foraccessories to hospitals and surgery centers (sold to Dalian JiKang Medical Systems September 1, 2015) and on the repair, maintenance and replacement parts on various products. The Professional segment generated revenues from the sale of equipment, such as lasers, medical and esthetic light and heat based products and LED products. At the current time, we operate the real estate business in one segment.

Results of Operations

The following table sets forth key components of our results of operations during the years ended December 31, 2014, 20132017 and 2012, respectively. We use2016, both in dollars and as a mixpercentage of direct-to-consumer advertising that includes infomercials, commercials, catalogour revenues.


(All dollar amounts in thousands)

  Year Ended December 31, 
  2017  2016 
  Amount  Amount 
Revenues $  $ 
Cost of revenues      
Gross profit      
Operating expenses:        
General and administrative expenses  10,817    
Impairment of investment in other company  862     
Loss from continuing operations before interest and other financing expense, net  (11,679)   
Revaluation of asset contribution related financial instruments, net  (1,392)   
Revaluation of Option to purchase redeemable convertible B preferred stock  (3,018)   
Interest and other financing expense, net  (267)   
Loss from continuing operations  (16,356)   
Discontinued operations:        
Loss from discontinued operations, net of taxes  (2,459)  (13,264)

Net loss

 $(18,815) $(13,264)

General and internet-based marketing campaigns, coupled with select retail resellers, such as Neiman Marcus, Henri Bendel, Planet Beauty, Bed, Bath & Beyond and others; home shopping channels such as HSN; and online retailers such as Dermadoctor.com and Drugstore.com. We believe these channels complement each other, as consumers that have seen our direct-to-consumer advertising may purchase at our retailers, and those who have seen our solutions demonstrated at our retailers may purchase solutions through our websites or call centers.

Administrative ExpensesInternational (excluding North America). Outside North America sales were approximately $30.3 million, $40.6 million and $47.0 million forFor the yearsyear ended December 31, 2014, 20132017, general and 2012, respectively. We utilize various salesadministrative expenses were approximately $10.82 million. For the year ended December 31, 2016 general and marketing methods including sales by direct-to-consumer, salesadministrative expenses were included in the loss from discontinued operations, (see Note 2 Discontinued Operations, to retailersour consolidated financial statements).

Impairment of Investment in Other Company.The Company evaluates investments in other company for impairment whenever events or changes in circumstances indicate that the carrying amount of an investment may not be recoverable in accordance with ASC 320 “Investments - Debt and home shopping channels. Our main international targeted markets include Asia Pacific, Europe and South America.

Physician Recurring
Physician recurring sales primarily include those generated from two of our product lines: (1) XTRAC® lasers, a noninvasive, FDA-cleared solution for psoriasis and vitiligo, and (2) NEOVA® skin care, a topical therapy combining DNA repair enzymes and copper peptide complexes to prevent premature skin aging. Both XTRAC and NEOVA represent recurring revenue streams with significant market opportunities. In addition, our expertiseEquity Securities”. The judgments regarding declines in direct-to-consumer advertising and innovative marketing programs is anticipated to drive greater brand awareness and adoption for both XTRAC and NEOVA products.
XTRAC®
The XTRAC business is considered a recurring revenue stream given its pay-per-use model, where the machinesvalue are provided to professionals who then pay us based on operating performance, market conditions and the numberCompany’s ability and intent to hold as well as its ability to influence significant decisions of treatments administeredthe venture. During the year ended December 31, 2017, based on managements’ most recent analyses, impairment losses have been identified related to the Company’s investment in other company amounting to $862.

Revaluation of Asset Contribution. For the year ended December 31, 2017, the revaluation of asset contribution increased to approximately $1.39 million due to the re-measurement of the asset contribution that resulted in a loss due to the reduced fair value of the asset.

Revaluation of Option to Purchase Redeemable Convertible B Preferred Stock.For the year ended December 31, 2017, the revaluation of the option to purchase redeemable convertible B preferred stock increased to approximately $3.0 million due to excess of the initial value of the option liability over the proceeds received, net with the device. We have historically employed a direct sales force marketing primarily to dermatologists to create awarenesschanges in the fair value of the XTRAC therapy. Beginning in 2012 we initiated direct to patient XTRAC advertising inOption at December 31, 2017.

Interest and Other Financing Expense, Net. Net interest and other financing expense for the United States targeted at psoriasis and vitiligo patients through testing a varietyyear ended December 31, 2017 was approximately $0.27 million. The functional currency of media including television and radio. We continue to increase our advertising expenditures in this area to reach the more than 10 million patients in the United States afflicted with these diseases.

NEOVA®
Salesall U.S. members of the NEOVA skin care products at present are driven by physicians, who actgroup, as spokespersons to their patientswell as Radiancy Ltd. (Israel), is the U.S. Dollar. The other foreign subsidiaries’ functional currency is each subsidiaries’ respective local currency. 

Loss. The factors discussed above resulted in support of the NEOVA line. We have historically marketed to physicians in the dermatology and plastic surgery field, but plan to supplement these efforts with a direct-to-consumer approach to lead patients into those practices. NEOVA addresses a sizeable global market for anti-aging skin care products. In addition, we have increased marketing exposure to NEOVA by offering an introduction to the product line as an added-value purchase to consumers responding to our no!no! brand advertising.

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Professional
Sales under the professional business segment are mainly generated from capital equipment, such as our XTRAC-Velocity and VTRAC equipment, our LHE® brand products and our Omnilux and Lumière Light Therapy systems.
We possess a greatly expanded product offering for the physician community. We have a 48-person, experienced direct sales force that already reaches a networknet loss, including discontinued operations, of approximately 3,000 physician locations in$18.82 million during the U.S. We also distribute through this direct sales forceyear ended December 31, 2017, as compared to net loss of approximately $13.26 million during the LHE-based professional products in addition to our other equipment to physicians, dermatologists, salons, spas,year ended December 31, 2016.

Liquidity and other aesthetic practitioners. We view this fully trained sales staff as a resource in expanding the Professional segment of our revenues.

Sales and Marketing
Capital Resources

As of December 31, 2014,2017, we had a deficit approximately $2.71 million of working capital compared to a deficit of approximately $2.35 million as of December 31, 2016. Cash and cash equivalents were approximately $0.95 million as of December 31, 2017, as compared to approximately $2.68 million as of December 31, 2016.


The following table provides detailed information about our salesnet cash flow for all financial statement periods presented in this report:

Cash Flow

 (In thousands)

  Year Ended December 31, 
  2017  2016 
Net cash provided by (used in) operating activities $(9,298) $358 
Net cash provided by investing activities  6,797   2,148 
Net cash provided by (used in) financing activities  906   (684)
Effect of exchange rate changes on cash  208   (2,789)
Net decrease in cash and cash equivalents  (1,387)  (967)
Cash and cash equivalents at beginning of year  2,335   3,302 
Cash and cash equivalent at end of year $948  $2,335 

Net cash and marketing personnel consistedused in operating activities was approximately $9.3 million for the year ended December 31, 2017 compared to approximately $0.36 million net cash provided by operating activities for the year ended December 31, 2016. The primary reason for the change was loss on asset sale to ICTV and the significant reductions in accounts payable and accrued liabilities settled during the year ended December 31, 2017.

Net cash provided by investing activities was approximately $6.8 million for the year ended December 31, 2017 compared to approximately $2.15 million for the year ended December 31, 2015. The primary reason for the change was the cash received from the sale of 92 full-time positions.the consumer division to ICTV for the year ended December 31, 2017.

Net cash provided by (used in) financing activities was approximately $0.9 million for the year ended December 31, 2017 compared to approximately $0.68 million net cash used in financing activities for the year ended December 31, 2016. The increase was due to the funding received from OFI in December 2017.

We have historically financed our activities with cash from operations, the private placement of equity and debt securities, borrowings under lines of credit and, in the most recent periods with sale of certain assets and business units.

On January 23, 2017, we sold our consumer products division to ICTV for a total selling price of $9.5 million, (see Note 2 Discontinued Operations, to our consolidated financial statements). We collected $5 million of that purchase price and the remaining amount of up to $4.5 million was to be payable through a contingent royalty on the sale of consumer products by ICTV. That royalty was settled in July 2017 for a payment of $2 million to our company.  Furthermore, while the Company is a party to a Securities Purchase Agreement with Opportunity Fund I-SS, LLC, and has raised certain funds under that Agreement, Opportunity Fund has no obligation to continue to invest in the Company, and there are restrictions placed by Opportunity Fund on the use of these funds.

On December 22, 2017, we entered into the Purchase Agreement with OFI, under which OFI may invest up to $15 million in our company in a series of closings, in exchange for which OFI will receive shares of our newly designated Series B Preferred Stock at a purchase price of $1.00 per share. On December 22, 2017, we completed the first closing under the Purchase Agreement, pursuant to which OFI provided $1.5 million to us. On January 24, 2018, we completed a second closing under the Purchase Agreement, pursuant to which OFI provided approximately $2.2 million to us in. Under the Purchase Agreement, OFI may, but is not obligated to, make additional investments in one or more subsequent closings until an aggregate amount of $15 million has been invested or the Purchase Agreement has been terminated in accordance with its terms. OFI has no obligation to continue to invest in our company, and there are restrictions placed by OFI on the use of these funds.

We will be required to obtain additional liquidity resources in order to support our operations. At this time, there is no guarantee that we will be able to obtain an adequate level of financial resources required for the short and long-term support of our operations or that we will be able to obtain additional financing as needed, or meet the conditions of such financing, or that the costs of such financing may not be prohibitive.

Off-Balance Sheet Arrangements

At December 31, 2017, we had no off-balance sheet arrangements.


Impact of Inflation

We have not operated in a highly inflationary period, and we do not believe that inflation has had a material effect on our revenues or expenses.

Critical Accounting Policies

The discussion and analysis of our financial condition and results of operations in this Report are based upon our Consolidated Financial Statements, which have been prepared in accordance with accounting principles generally accepted in the United States.GAAP. The preparation of financial statements requires management to make estimates and judgments that affect the reported amounts of assets and liabilities, revenues and expenses and disclosures at the date of the financial statements. On an on-going basis, we evaluate our estimates, including, but not limited to, those related to revenue recognition, accounts receivable, inventories, impairment of property and equipment and of intangibles and accruals for warranty claims. We use authoritative pronouncements, historical experience and other assumptions as the basis for making estimates. Actual results could differ from those estimates.

Management believes that the following critical accounting policies affect our more significant judgments and estimates in the preparation of our Consolidated Financial Statements. These critical accounting policies and the significant estimates made in accordance with these policies have been discussed with our Audit Committee.

Acquisition of Investment Properties.The Company allocates the purchase price of real estate to identifiable tangible assets such as land, building, land improvements and tenant improvements acquired based on their fair value. In estimating the fair value of each component management considers appraisals, replacement cost, its own analysis of recently acquired and existing comparable properties, market rental data and other related information. The Company’s investment properties as of December 31, 2017 were acquired on May 17, 2017, and included four vacant land sites set for development into gas stations. The Company determined that the fair value of these investment properties on the acquisition date was $2,600.

Impairment of Investment Properties. Our long-lived assets include mainly these investment properties. The Company periodically evaluates its long-lived assets, including investment properties, for indicators of impairment in accordance with ASC 360, “Property, Plant, and Equipment”, whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable. The judgments regarding the existence of indicators of impairment are based on the operating performance, market conditions, as well as the Company’s ability to hold and its intent with regard to each property. The judgments regarding whether the carrying amounts of these assets may not be recoverable are based on estimates of future undiscounted cash flows from properties which include estimates of future operating performance and market conditions. During the year ended December 31, 2017, based on managements’ most recent analyses, impairment losses related to the Company’s investment properties have not been identified.

Impairment of Investment in Other Company.The Company evaluates investments in other company for impairment whenever events or changes in circumstances indicate that the carrying amount of an investment may not be recoverable in accordance with ASC 320 “Investments - Debt and Equity Securities”. The judgments regarding declines in value are based on operating performance, market conditions and the Company’s ability and intent to hold as well as its ability to influence significant decisions of the venture. During the year ended December 31, 2017, based on managements’ most recent analyses, impairment losses have been identified related to the Company’s investment in other company amounting to $862.

Option to Purchase Redeemable Convertible B Preferred Stock.The fair value of the option to purchase redeemable convertible B preferred stock that was issued to an investor in connection with a securities purchase agreement in December 2017 (the Initial Date) was estimated using the Black-Scholes-Merton option-pricing model. We accounted for the aforesaid option according to the provisions of ASC 480, “Distinguishing Liabilities from Equity” since the option is considered freestanding, as the Company believes it is legally detachable and separately exercisable. In addition, the option is exercisable for Convertible B Preferred Stock which are subject to possible redemption at the option of the holder. We classified the option as non-current liability, remeasured at fair value each reporting period until the option will be exercised or expired, with changes in the fair values being recognized in our statement of comprehensive loss as financial income or expense. The fair value of the Option was estimated at the Initial Date and December 31, 2017 by using hybrid method that includes scenario of conversion and scenario liquidation and the Black-Scholes option pricing model. In the first scenario, the Series B Preferred Stock price applied in the model was assumed based on the as-converted price on the date of estimation. Expected volatility was estimated by using a group of peers in the real estate development, homebuilding and income-producing properties sectors, and applying a 75% percentile ranking based on the total capitalization of the Company. In the second scenario, the option was estimated based on the value of the option in a proposed liquidation scenario. A probability weighting was applied to determine the expected value of the option. During the year ended December 31, 2017, the Company recorded a loss amounting to $4,084 as an excess of the initial value of the option liability over the proceeds received and income from revaluation of the option to purchase redeemable convertible B preferred stock in total amount of $1,194.

Revenue Recognition. We recognizerecognized revenues from the product sales when the following four criteria have beenwere met: (i) the product hashad been shipped and we havehad no significant remaining obligations; (ii) persuasive evidence of an arrangement exists;existed; (iii) the price to the buyer iswas fixed or determinable; and (iv) collection iswas probable. Revenues from product sales arewere recorded net of provisions for estimated chargebacks, rebates, expected returns and cash discounts.

We shipshipped most of our products FOB shipping point, although from time to time certain customers, for example governmental customers, will insist upon FOB destination. Among the factors we taketook into account when determining the proper time at which to recognize revenue arewas when title to the goods transferstransferred and when the risk of loss transfers.transferred. Shipments to distributors or physicians that dodid not fully satisfy the collection criterion arewere recognized when invoiced amounts arewere fully paid or fully assured.

For revenue arrangements with multiple deliverables within a single contractually binding arrangement (usually sales of products with separately priced extended warranty), each element of the contract is accounted for as a separate unit of accounting when it provides the customer value on a stand-alone basis and there is objective evidence of the fair value of the separate, but related, unit.

With respect to sales arrangements under which the buyer hashad a right to return the related product, revenue iswas recognized only if all the following arewere met: the price iswas fixed or determinable at the date of sale; the buyer hashad paid, or iswas obligated to pay and the obligation iswas not contingent on resale of the product; the buyer'sbuyer’s obligation would not be changed in the event of theft or physical destruction or damage of the product; the buyer hashad economic substance; we dodid not have significant obligations for future performance to directly bring about resale of the product by the buyer; and the amount of future returns cancould be reasonably estimated.

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We provideprovided a provision for product returns based on the experience with historical sales returns, in accordance with ASC Topic 605-15 with respect to sales of product when right of return exists. As of December 31, 2014, accrued sales returns provision was $7,651 or 4.7% of total recognized revenues of $163,541. As of December 31, 2013, accrued sales returns provision was $16,046 or 7.1% of total recognized revenues of $224,664. The return provisions are influenced by product mix and in 2014 there was lower rate toward the direct channel.

Revenues received with respect to extended warranty on consumer products are recognized over the duration of the warranty period. As of December 31, 2014, deferred revenues for the extended warranties amounted to $5,467 or 3.3% on total recognized revenues. As of December 31, 2013, deferred revenues for the extended warranties amounted to $8,496 or 3.8% on total recognized revenues.  During 2013, we began to sell extended warranties in both UK and Germany.

Inventories. We have two distribution channels for our phototherapy treatment equipment. We either (i) sell our lasers through a distributor or directly to a physician or (ii) place our lasers in a physician's office (at no charge to the physician) and generally charge the physician a fee for an agreed upon number of treatments. In some cases, the customer and we stipulate to a quarterly or other periodic target of procedures to be performed, and accordingly revenue is recognized ratably over the period.

When we place a laser in a physician's office, we generally recognize service revenue based on the number of patient treatments performed, or purchased under a periodic commitment, by the physician. Treatments to be performed through random laser-access codes that are sold to physicians free of a periodic commitment, but not yet used, are deferred and recognized as a liability until the physician performs the treatment. Unused treatments remain an obligation of the Company because the treatments can only be performed on equipment which we own and place with the customer. Once the treatments are delivered to a patient, this obligation has been satisfied. We defer substantially all sales of treatment codes ordered by and delivered to its customers within the last two weeks of the period in determining the amount of procedures performed by its physician-customers. Management believes this approach closely approximates the actual amount of unused treatments that existed at the end of a period. As of December 31, 2014, we have deferred treatment code revenues of $98 or 0.4% of total recognized treatment revenues of $22,871. As of December 31, 2013, we have deferred treatment code revenues of $172 or 1.1% of total recognized treatment revenues of $15,489. As of December 31, 2012, we have deferred treatment code revenues of $504 or 6.0% of total recognized treatment revenues of $8,441.
Revenue from maintenance service agreements is deferred and recognized on a straight-line basis over the term of the agreements. Revenue from billable services, including repair activity, is recognized when the service is provided.
Inventory.  We account for inventorycarried inventories at the lower of cost or market. Cost iswas determined to be purchased cost for raw materials and the production cost (materials, labor and indirect manufacturing cost) for work-in-process and finished goods. For our consumer and LHE products, cost iswas determined on the weighted-average method. For the pre-merged PhotoMedex'sPhysician market products, cost iswas determined on the first-in, first-out method. Throughout the laser manufacturing process, the related production costs are recorded within inventory. Work-in-process is immaterial, given the typically short manufacturing cycle, and therefore is disclosed in conjunction with raw materials. We perform full physical inventory counts for XTRAC and cycle counts on the other inventory to maintain controls and obtain accurate data.
Our XTRAC laser is either (i) sold to distributors or physicians directly or (ii) placed in a physician's office and remains our property. The cost to build a laser, whether for sale or for placement, is accumulated in inventory. When a laser is placed in a physician's office, the cost is transferred from inventory to "lasers in service" within property and equipment. At times, units are shipped to distributors, but revenue is not recognized until all of the Criteria have been met, and until that time, the unit is carried on our books as inventory. Revenue is not recognized from these distributors until payment is either assured or paid in full.
Reserves for slow-moving, excess and obsolete inventories reduce the historical carrying value of our inventories and arewere provided based on historical experience and product demand. Management evaluatesevaluated the adequacy of these reserves periodically based on forecasted sales and market trends.
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There is no value to the remaining inventory as of December 31, 2017. The inventories as of December 31, 2016 were classified as assets held for sale.

Allowance for Doubtful Accounts. Accounts receivable arewere reduced by an allowance for amounts that may become uncollectible in the future. From time to time, our customers disputedisputed the amounts due to us, and, in other cases, our customers experienceexperienced financial difficulties and cannotcould not pay on a timely basis. In certain instances, these factors ultimately result in uncollectible accounts. The determination of the appropriate reserve needed for uncollectible accounts involves significant judgment. Such factors include changes in the financial condition of our customers as a result of industry, economic or customer-specific factors. A change in the factors used to evaluate collectability could result in a significant change in the allowance needed. As of December 31, 20142017 and 2013,2016, the allowance for doubtful accounts was $13,559$0 and $10,734approximately $1.19 million, or 8.3%0% and 4.8%3.1%, respectively of the total recognized revenues of each year.


The allowance for doubtful accounts provisions are influenced by product mix and in 2013 there was higher rate toward the direct channel.

Property and Equipment.  As of December 31, 2014 and 2013, we had net property and equipment of $13,802 and $10,489, respectively. The most significant component relates to the XTRAC lasers placed by us in physicians' offices. We own the equipment and charge the physician on a per-treatment basis for use of the equipment. The recoverability of the net carrying value of the lasers is predicated on continuing revenues from the physicians' use of the lasers. If the physician does not generate sufficient treatments, then we may remove the laser from the physician's office and redeploy elsewhere. XTRAC lasers placed in service are depreciated on a straight-line basis over the estimated useful life of five-years. For other property and equipment depreciation is calculated on a straight-line basis over the estimated useful lives of the assets, primarily three to seven years for computer hardware and software, furniture and fixtures, automobiles and machinery and equipment. Leasehold improvements are amortized over the lesser of the useful lives or lease terms. Useful lives are determined based upon an estimate of either physical or economic obsolescence, or both.
Goodwill and Intangibles Assets. As part of the purchase price allocation for the 2011 reverse acquisition, we recorded goodwill in the amount of $24,005 and definite-lived intangibles in the amount of $12,000. Goodwill reflected the value or premium of the acquisition price in excess of the fair values assigned to specific tangible and intangible assets. Goodwill had an indefinite useful life and therefore was not amortized as an expense but was reviewed annually for impairment of its fair value to our company. Activity in goodwill during the year ended December 31, 2016 follows (in thousands):.
Our balance sheet includes

Balance at January 1, 2016 $3,581 
Disposal on sale of assets  (1,039)
Impairment of goodwill  (2,257)
Translation differences  (285)
Balance at December 31, 2016 $ 

During the third quarter of 2016, we recorded goodwill and other intangible asset impairment charges of approximately $3.52 million, as we determined that a portion of the value of our goodwill and other intangible assets which affect the amount of future period amortization expense and possible impairment expense that we will incur. Management's judgments regarding the existence of impairment indicators, on an interim or annual basis, are based on various factors, including market conditions and operational performance of our business. As of December 31, 2014 and 2013, we had $41,196 and $45,463 of goodwill and other intangibles, accounting for 22% and 21% of our total assets, respectively. The goodwill is not amortizable; the other intangibles are. The determination of the value of such intangible assets requires management to make estimates and assumptions that affect our consolidated financial statements. We test our goodwill for impairment, which was acquired as part of the reverse acquisition on December 13, 2011, at least annually. This test is conducted in December of each yearimpaired in connection with the annual budgetingthen pending transaction with ICTV. We recorded an impairment of the entire remaining balance of Consumer segment goodwill in the amount of approximately $2.26 million and forecast process. Also, on a quarterly basis, we evaluate whether events or changesrecorded the impairment of the Consumer segment of the intangibles for its licensed technology in circumstances have occurred that would negatively impact the realizable valueamount of approximately $1.26 million (see Note 2 Discontinued Operations, to our intangibles or goodwill.

consolidated financial statements). We reorganized our business into three operating units, excluding LCA, which resulted in a change in reporting segments effective December 13, 2011. For the purposesderecognized an amount of approximately $1.04 million of goodwill impairment testing, our reporting units are defined as Consumer,related to the Physician Recurring and Professional Equipment. The balance of our goodwill for each of our segments as of December 31, 2014 is as follows: Consumer $19,968, Physician Recurring $4,080 and Professional Equipment $0. We completed our annual goodwill impairment analysis as of December 31, 2014 for our consumer and physician recurring reporting units. Our assessment concluded that there was not any impairment of goodwill. Our analysis employed the use of both a market and income approach, with each method given equal weighting. Significant assumptions usedsegment in the income approach include growth and discount rates, margins and the Company's weighted average cost of capital. We used historical performance and management estimates of future performance to determine margins and growth rates. Discount rates selected for each reporting unit varied. Our weighted average cost of capital included a review and assessment of market and capital structure assumptions. Of the two reporting units with goodwill, Consumer has a fair value that is in excess of its carrying value by approximately 209%, while Physician Recurring has a fair value that is approximately 169% in excess of its carrying value. Considerable management judgment is necessary to evaluate the impact of operating changes and to estimate future cash flows. Changes in our actual results and/or estimates or any of our other assumptions used in our analysis could result in a different conclusion.
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In connection with the reverse acquisitionasset sale of Pre-merged PhotoMedex on December 31, 2011, we acquired certain intangibles recorded atthe Neova product line.

Stock-based compensation. We account for stock based compensation to employees in accordance with the “Share-Based Payment” accounting standard. The standard requires estimating the fair value as of equity-based payment awards on the date of acquisition.grant using an option-pricing model. The balancesvalue of these acquired intangibles,the portion of the award that is ultimately expected to vest is recognized as an expense over the requisite service periods in our consolidated statement of operations. The fair value of employee stock options is estimated using a Black-Scholes valuation model. The fair value of restricted shares is based on the quoted market price of our common stock on the date of issuance. Compensation costs for share-based payment awards are recorded using the graded vesting attribution method over the vesting period, net of amortization, were:

December 31, 2014
Customer Relationships$   4,376
Tradename3,961
Product and Core Technologies8,811
Goodwill24,048
     Total$ 41,196
estimated forfeitures.

Income taxes.As part of the process of preparing our consolidated financial statements, we are required to estimate our income taxes in each of the jurisdictions in which we operate. This process requires us to estimate our actual current tax exposure and make an assessment of temporary differences resulting from differing treatment of items, for tax and accounting purposes. These differences result in deferred tax assets and liabilities, which are included within our consolidated balance sheet. We must then assess the likelihood that our deferred tax assets will be recovered from future taxable income and, to the extent we believe that recovery is more likely than not, we establish a valuation allowance. After evaluating the effectsAt year end December 31, 2016, material amounts of valuation allowances were recorded representing: 100% of the reverse merger and integration of Radiancy's business on its net operating lossesdeferred tax assets in the U.K., management determinedUS and in the UK. Our assessment for the year ended December 31, 2017, is that the NOLs remain usable against future income of the U.K. subsidiary.a 100% valuation allowance is still required. To the extent we establish a valuation allowance or increase this allowance in a period, we must include an expense within the tax provision in the consolidated statement of operations. Significant management judgment is required in determining our deferred tax assets and liabilities and any valuation allowance recorded against our net deferred tax assets. In the event that we generate taxable income in the jurisdictions in which we operate and in which we hashave net operating loss carry-forwards that we can utilize to offset all or part of this taxable income, we may be required to adjust our valuation allowance.

On December 22, 2017, the U.S. government enacted comprehensive tax legislation commonly referred to as the Tax Cuts and Jobs Act or the Tax Act. The Tax Act makes broad and complex changes to the U.S. tax code, including, but not limited to, reducing the U.S. federal corporate tax rate from 35 percent to 21 percent; eliminating the corporate alternative minimum tax or AMT and changing how existing AMT credits can be realized; creating a new limitation on deductible interest expense; changing rules related to uses and limitations of net operating loss carryforwards created in tax years beginning after December 31, 2017; limitations on the deductibility of certain executive compensation.

In December 2017, the SEC issued Staff Accounting Bulletin No. 118, or SAB 118, which addresses situations where the accounting is incomplete for the income tax effects of the Act. SAB 118 directs taxpayers to consider the impact of the Act as “provisional” when a company does not have the necessary information available, prepared or analyzed (including computations) to finalize the accounting for the change in tax law. Companies are provided a measurement period of up to one year to obtain, prepare, and analyze information necessary to finalize the accounting for provisional amounts or amounts that cannot be estimated as of December 31, 2017.

With regards to the Tax Act impact on the tax provision as it relates to the company for period year-ending December 31, 2017, we have recognized the provisional impact of tax reform related to the revaluation of deferred tax assets and liabilities from 35% to 21% of $17.2 million tax expense, which is offset by a reduction in the valuation allowance.


In the years ended December 31, 2017 and 2016, we reported financial results for both operations and discontinued operations. ASC 740-20-45 sets down the general rule for allocating income tax expense or benefit between operations and discontinued operations. The general rule requires the computation of tax expense or benefit by entity taking into consideration all items of income, expense, and tax credits. Next, a computation is made taking into consideration only those items related to continuing operations. Any difference is allocated to items other than continuing operations e.g. discontinued operations. Under these general rules, no tax expense or benefit would be allocated to discontinued operations.

An exception to these rules apply under ASC 740-20-45-7 where an entity has 1) a loss from continuing operations and income related to other items such as discontinued operations and 2) the entity would not otherwise recognize a benefit for the loss from continuing operations under the approach described in ASC 740-20-45. This fact pattern applies for the years ended December 31, 2016 for entities in the US and the UK. Application of this rule exception results in the allocation of tax expense to discontinued operations with an offsetting amount of tax benefit reported by the US and UK companies.

We implementedfollow ASC Topic 740-10, "Income Taxes"“Income Taxes” which clarifyclarifies the accounting for uncertainty in tax positions. ASC Topic 740-10 requires that we recognize in our financial statements the impact of a tax position, if that position will more likely than not be sustained upon examination, based on the technical merits of the position, without regard the likelihood that the tax position may be challenged. If an uncertain tax position meets the "more-likely-than-not"“more-likely-than-not” threshold, the largest amount of tax benefit that is greater than 50% likely to be recognized upon ultimate settlement with the taxing authority is recorded.

Stock-based compensation. We account for stock based compensation to employees in accordance with "Share-Based Payment" accounting standard. The standard requires estimating the fair value of equity-based payment awards on the date of grant using an option-pricing model. The value of the portion of the award that is ultimately expected to vest is recognized as an expense over the requisite service periods in our consolidated statement of operations.
The fair value of employee stock options is estimated using a Black-Scholes valuation model. Compensation costs are recorded using the graded vesting attribution method over the vesting period, net of estimated forfeitures.

The total share-based compensation expense was $4,938approximately $1.47 million and $4,985approximately $1.97 million for the years ended December 31, 20142017 and 2013,2016, respectively.

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Results

Recent Accounting Pronouncements

Recent Accounting Pronouncements Adopted

On March 30, 2016, the FASB issued ASU 2016-09, “Compensation-Stock Compensation”, which effects all entities that issue share-based payment awards to their employees. The amendments in this update cover such areas as the recognition of Operations

Revenues
The following table illustrates revenues by type from our three business segmentsexcess tax benefits and deficiencies, the classification of those excess tax benefits on the statement of cash flows, an accounting policy election for the periods listed below:
  For the Year Ended December 31, 2014 
  Product Sales  Services  Total 
Consumer $120,931  $-  $120,931 
Physician Recurring  11,369   22,871   34,240 
Professional  8,370   -   8,370 
             
Total Revenues $140,670  $22,871  $163,541 

  For the Year Ended December 31, 2013 
  Product Sales  Services  Total 
Consumer $188,259  $-  $188,259 
Physician Recurring  13,059   15,489   28,548 
Professional  7,857   -   7,857 
             
Total Revenues $209,175  $15,489  $224,664 

  For the Year Ended December 31, 2012 
  Product Sales  Services  Total 
Consumer $188,425  $-  $188,425 
Physician Recurring  12,843   8,441   21,284 
Professional  10,942   -   10,942 
             
Total Revenues $212,210  $8,441  $220,651 

Revenues from our Clinics segment, inforfeitures, the amount an employer can withhold to cover income taxes and still qualify for equity classification and the classification of $47,197those taxes paid on the statement of cash flows. This update is effective for annual and interim periods beginning after December 15, 2016. This guidance can be applied either prospectively, retrospectively or using a modified retrospective transition method. We adopted the period of May 13 through December 31, 2014,new guidance prospectively. This new guidance does not have been accounted for as a discontinued operation. There were no corresponding revenues for the years ended December 31, 2013 and 2012 as LCA Vision was acquired on May 13, 2014.
Consumer Segment
The following table illustrates the key changes in the revenues of the Consumer segment, by sales channel, for the periods reflected below:
  For the Year Ended December 31, 
  2014  2013  2012 
Direct-to-consumer $86,709  $130,785  $125,208 
Distributors  1,865   15,553   24,851 
Retailers and home shopping channels  32,357   41,921   38,366 
             
Total Consumer Revenues $120,931  $188,259  $188,425 

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For the year ended December 31, 2014, consumer segment revenues were $120,931 compared to $188,259 in the year ended December 31, 2013. The revenues decreased between the years mainly due to the following reasons:
Direct to Consumer. Revenues for the year ended December 31, 2014 were $86,709 compared to $130,785 for the year ended December 31, 2013. The decrease of 34% was due to management's decision to significantly reduce amounts spent on short-form TV advertising during the period due to highly irregular response rates from this format as well as limited availability of relevant media at attractive cost-effective pricing. The decrease in revenue also has anmaterial impact on the total amount of sales returns liability as reflected in Note 9 of the financial statement footnotes. The methodology used to determine both the expense and the accrued liability has been consistently applied across all periods presented.
Retailers and Home Shopping Channels. Revenues for the year ended December 31, 2014 were $32,357 compared to $41,921 for the year ended December 31, 2013. The decrease of 23% was mainly due to the timing of specials on the various home shopping channel customers, mainly in the United States ("US") and the United Kingdom ("UK"). Furthermore, reduced levels of advertising in the Direct to Consumer channel negatively impacts sales as the retail level.
Distributors Channels. Revenues for the year end December 31, 2014 were $1,865 compared to $15,553 for the same period in 2013. The decrease in revenues of 88% was due to our distributor in Japan who modified its business model during 2013, affecting its role in the supply chain between its manufacturers and the Japan retailers they supply and causing revenues from our Japan distributor to decrease to $227 from $10,920. During the fourth quarter of 2013, we terminated our distribution agreement with the Japan distributor.
For the year ended December 31, 2013, consumer segment revenues were $188,259 compared to $188,425 in the year ended December 31, 2012. The revenues remained consistent between the years but the sales channels changed mainly due to the following reasons:
Direct to Consumer. Revenues for the year ended December 31, 2013 were $130,785 compared to $125,208 for the year ended December 31, 2012. The increase of 4% was mainly due to our successful marketing programs which have led to year-over-year revenue growth. Additionally, in 2013, we launched marketing programs in Germany, resulting in approximately $712 in revenues, and Brazil, resulting in approximately $421 in revenues, for the year ended December 31, 2013.
Retailers and Home Shopping Channels. Revenues for the year ended December 31, 2013 were $41,921 compared to $38,366 for the year ended December 31, 2012. The increase of 9% was also mainly due to our successful marketing programs to the various home shopping channel customers, mainly in the US and the UK and to the additional retailers added to this channel.
Distributors Channels. Revenues for the year end December 31, 2013 were $15,553 compared to $24,851 for the same period in 2012. The decrease in revenues of 37% was due to our distributor in Japan who modified its business model during 2013, affecting its role in the supply chain between its manufacturers and the Japan retailers they supply and causing revenues from our Japan distributor to decrease to $10,920 from $19,276. During the fourth quarter of 2013, we cancelled our distribution agreement with the Japan distributor.

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The following table illustrates the key changes in the revenues of the Consumer segment, by markets (determined by ship to locations), for the periods reflected below:
  For the Year Ended December 31, 
  2014  2013  2012 
North America $90,643  $147,682  $141,478 
International  30,288   40,577   46,947 
             
Total Consumer Revenues $120,931  $188,259  $188,425 

International revenues, excluding the decrease in Japan, increased by $404 and $2,390, respectively, over the prior year periods, which was partially due to our expansion in new international markets including Brazil, Germany, Hong Kong and Columbia.
Physician Recurring Segment
The following table illustrates the key changes in the revenues of the Physician Recurring segment for the periods reflected below:
  For the Year Ended December 31, 
  2014  2013  2012 
XTRAC Treatments $22,871  $15,489  $8,441 
Neova skincare  6,795   8,243   8,156 
Other  4,574   4,816   4,687 
             
Total Physician Recurring Revenues $34,240  $28,548  $21,284 
XTRAC Treatments
Recognized treatment revenue for the year ended December 31, 2014 was $22,871, which approximates 305,000 treatments with prices between $65 and $95 per treatment compared to recognized treatment revenue for the year ended December 31, 2013 was $15,489, which approximates 221,000 treatments with prices between $65 and $95 per treatment. Recognized treatment revenue for the year ended December 31, 2012 was $8,441, which approximates 125,000 treatments with prices between $65 and $85 per treatment. Increases in procedures are dependent upon building market acceptance with our physician partners and their patients that the XTRAC procedures will be of clinical benefit and will be generally reimbursed by insurers. We have historically employed a direct sales force marketing primarily to dermatologists to create awareness of the XTRAC therapy. Beginning in 2012 we initiated direct to patient XTRAC advertising in the United States targeted at psoriasis and vitiligo patients through testing a variety of media including television and radio. We continue to increase our advertising expenditures in this area to reach the more than 10 million patients in the United States afflicted with these diseases.
We defer substantially all sales of treatment codes ordered by and delivered to the customer within the last two weeks of the period in determining the amount of procedures performed by our physician-customers. Management believes this approach closely approximates the actual amount of unused treatments that existed at the end of a period. For the year ended December 31, 2014, we recognized net revenues of $65 under this approach. For the year ended December 31, 2013, we recognized net revenues of $312 under this approach.
NEOVA skincare
For the year ended December 31, 2014 revenues were $6,795 compared to $8,243 for the year ended December 31, 2012. For the year ended December 31, 2013 revenues were $8,156. These revenues are generated from the sale of various skin, hair and wound care products to physicians in both the domestic and international markets.
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The following table illustrates the key changes in the revenues of the Physicians Recurring segment, by markets (determined by ship to locations), for the periods reflected below:
  For the Year Ended December 31, 
  2014  2013  2012 
North America $30,714  $25,260  $18,607 
International  3,526   3,288   2,677 
             
Total Physicians Recurring Revenues $34,240  $28,548  $21,284 
Professional Segment
The following table illustrates the key changes in the revenues of the Professional segment for the periods reflected below:
  For the Year Ended December 31, 
  2014  2013  2012 
Dermatology equipment $5,025  $3,962  $4,174 
LHE equipment  1,849   2,240   4,241 
Other equipment  1,496   1,655   2,527 
             
Total Professional Revenues $8,370  $7,857  $10,942 
Dermatology equipment
For the years ended December 31, 2014, 2013 and 2012, dermatology equipment revenues were $5,025, $3,962 and $4,174, respectively. Included in the December 31, 2012 amount were domestic XTRAC laser sales of $899 on 20 lasers sold. There were no domestic XTRAC laser sales for the years ended December 31, 2014 and 2013. We sell the laser directly to the customer for certain reasons, including the costs of logistical support and customer preference. Our preference is to consign lasers to customers which will thrive under the per-procedure model. Internationally, we sold 118 systems for the year ended December 31, 2014, 54 of which were VTRAC systems, a lamp-based alternative UVB light source that has a wholesale sales price that is below our competitors' international dermatology equipment and below that of our XTRAC laser. We sold 115 systems for the year ended December 31, 2013, 64 of which were VTRAC systems. We sold 121 systems for the year ended December 31, 2012, 82 of which were VTRAC systems. The international sales of our XTRAC and VTRAC systems were $3,275 for the year ended December 31, 2012.
LHE® brand products
LHE® brand products revenues include revenues derived from the sales of mainly Mistral™, Kona™, FSD™, SpaTouch Elite™ and accessories. These devices are sold to physicians, spas and beauty salons.
For the years ended December 31, 2014 and 2013, LHE® brand products revenues were $1,849 and $2,240, respectively. For the year ended December 31, 2012 revenues were $4,241.
The following table illustrates the key changes in the revenues of the Professional segment, by markets (determined by ship to locations), for the periods reflected below:
  For the Year Ended December 31, 
  2014  2013  2012 
North America $1,804  $2,012  $3,026 
International  6,566   5,845   7,916 
             
Total Professional Revenues $8,370  $7,857  $10,942 
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Cost of Revenues: all segments
The following table illustrates cost of revenues from our three business segments for the periods listed below:
  For the Year Ended December 31, 2014 
  Product Sales  Services  Total 
Consumer $20,307  $-  $20,307 
Physician Recurring  5,499   7,219   12,718 
Professional  5,594   -   5,594 
             
Total Cost of Sales $31,400  $7,219  $38,619 

  For the Year Ended December 31, 2013 
  Product Sales  Services  Total 
Consumer $26,794  $-  $26,794 
Physician Recurring  6,216   6,806   13,022 
Professional  5,219   -   5,219 
             
Total Cost of Sales $38,229  $6,806  $45,035 

  For the Year Ended December 31, 2012 
  Product Sales  Services  Total 
Consumer $28,965  $-  $28,965 
Physician Recurring  6,428   5,084   11,512 
Professional  6,165   -   6,165 
             
Total Cost of Sales $41,558  $5,084  $46,642 

Overall, cost of revenues changed in each segment due to the related changes in revenues. Included in cost of revenues above are certain inventory excess and obsolete provisions of $421, $698 and $336 for the years ended December 31, 2014, 2013 and 2012, respectively.
Gross Profit Analysis
Gross profit decreased to $124,922 for the year ended December 31, 2014 from $179,629 during the same period in 2013. As a percentage of revenues, the gross margin decreased to 76.4% for the year ended December 31, 2014 from 80.0% for the same period in 2013.
Gross profit increased to $179,629 for the year ended December 31, 2013 from $174,009 during the same period in 2012. As a percentage of revenues, the gross margin increased to 80.0% for the year ended December 31, 2013 from 78.9% for the same period in 2012.
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The following table analyzes changes in our gross margin for the periods presented below:
Company Profit Analysis For the Year Ended December 31, 
  2014  2013  2012 
Revenues $163,541  $224,664  $220,651 
Percent (decrease) increase  (27.2%)  1.8%    
Cost of revenues  38,619   45,035   46,642 
Percent decrease  (14.2%)  (3.4%)    
Gross profit $124,922  $179,629  $174,009 
Gross margin percentage  76.4%  80.0%  78.9%
The primary reasons for the changes in gross profit and the gross margin percentage for the year ended December 31, 2014, compared to the same period in 2013, were due to a decrease in consumer revenues. Partly offsetting this, the Physician Recurring segment, which has a lower margin than the Consumer segment, had 20% greater revenues than the prior year period with a greater gross margin percentage driven by greater utilization of our installed base of XTRAC equipment.
The primary reasons for the changes in gross profit and the gross margin percentage for the year ended December 31, 2013, compared to the same period in 2012 were due to a change in the sales mix within the Consumer segment with the direct channel, having the highest product gross margins, growing faster than the distributor and retail channels. In addition the Physician Recurring segment had 34% greater revenues than the prior year period with a greater gross margin percentage driven by greater utilization of our installed base of XTRAC equipment.
The following table analyzes the gross profit for our Consumer segment for the periods presented below:
Consumer Segment For the Year Ended December 31, 
  2014  2013  2012 
Revenues $120,931  $188,259  $188,425 
Percent decrease  (35.8%)  (0.1%)    
Cost of revenues  20,307   26,794   28,965 
Percent decrease  (24.2%)  (7.5%)    
Gross profit $100,624  $161,465  $159,460 
Gross margin percentage  83.2%  85.8%  84.6%
Gross profit for the year ended December 31, 2014 decreased by $60,841 from the comparable period in 2013. Gross margin percentage for the year ended December 31, 2014 was 83.2%, compared to 85.8% for the year ended December 31, 2013. The Consumer segment had a decrease in revenues in the year ended December 31, 2014 compared to the prior year. This segment provides the highest gross margin of our segments, so changes to these revenues can significantly impact our overall gross margin.
Gross profit for the year ended December 31, 2013 increased by $2,005 from the comparable period in 2012. The key factor for this increase was an increase in the direct to consumer channel in North America via commercials, infomercials and online campaigns. Gross margin percentage for the year ended December 31, 2013 was 85.8%, compared to 84.6% for the year ended December 31, 2012. The improvement in gross margin was due to an increase in the direct to consumer sales channel, which has a higher gross margin compared to the other sales channels.
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The following table analyzes the gross profit for our Physician Recurring segment for the periods presented below:
Physician Recurring Segment For the Year Ended December 31, 
  2014  2013  2012 
Revenues $34,240  $28,548  $21,284 
Percent increase  19.9%  34.1%    
Cost of revenues  12,718   13,022   11,512 
Percent (decrease) increase  (2.3%)  13.1%    
Gross profit $21,522  $15,526  $9,772 
Gross margin percentage  62.9%  54.4%  45.9%
Gross profit for the year ended December 31, 2014 increased by $5,996 from the year ended December 31, 2013. Gross profit for the year ended December 31, 2013 increased by $5,754 from the year ended December 31, 2012. The primary reason for the increased gross profits and gross margins is the increase in XTRAC treatments on the existing installed laser base of equipment. Incremental treatments delivered on existing equipment incur negligible incremental costs.
The following table analyzes the gross profit for our Professional segment for the periods presented below:
Professional Segment For the Year Ended December 31, 
  2014  2013  2012 
Revenues $8,370  $7,857  $10,942 
   Percent increase (decrease)  6.5%  (28.2%)    
Cost of revenues  5,594   5,219   6,165 
   Percent increase (decrease)  7.2%  (15.3%)    
Gross profit $2,776  $2,638  $4,777 
Gross margin percentage  33.2%  33.6%  43.7%
Gross profit for the year ended December 31, 2014 remained consistent with the comparable period in 2013. For the year ended December 31, 2014, the gross margin percentage was 33.2% compared to 33.6% for the year ended December 31, 2013.
Gross profit for the year ended December 31, 2013 decreased by $2,139 from the comparable period in 2012. For the year ended December 31, 2013, the gross margin percentage was 33.6% compared to 43.7% for the year ended December 31, 2012. The key factor for the decreases was the decreases in revenues for each product type and the gross margin change is affected by the mix of products sold and the mix of channels where they are sold.
Engineering and Product Development
Engineering and product development expenses for the year ended December 31, 2014 decreased to $3,086 from $3,306 for the year ended December 31, 2013. Engineering and product development expenses for the year ended December 31, 2013 increased to $3,306 from $2,914 for the year ended December 31, 2012. The majority of this expense relates to the salaries of our worldwide engineering and product development team and are in line with the prior year.
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Selling and Marketing Expenses
For the year ended December 31, 2014, selling and marketing expenses decreased to $107,169 from $127,528 for the year ended December 31, 2013 for the following reasons:
We decreased no!no! Hair Removal direct to consumer activities in North America due to management's decision to significantly reduce amounts spent on short-form TV advertising during the period as a result of highly irregular response rates from this format. We continuously monitor the performance on all of our media avenues and when results are not as expected, we reduce and/or change the affected areas of our media.
Overall media buying and advertising expenses in the year ended December 31, 2014 were 38.0% of total revenues compared to 32.0% of total revenues in the year ended December 31, 2013. There was change in the mix of revenues toward business channels and segments that are less dependent upon the level of advertising investment. Direct to consumer revenues are 53% of total revenues for the year ended December 31, 2014 compared to 58.2% of total revenues for the year ended December 31, 2013. In addition, we added new marketing initiatives to support Neova, Kyrobak, XTRAC therapy, as well as no!no! hair in Brazil and Germany spending approximately $6,722 compared to $4,645 for the year ended December 31, 2013.
For the year ended December 31, 2013, selling and marketing expenses increased to $127,528 from $116,487 for the year ended December 31, 2012 for the following reasons:
We increased no!no! Hair Removal direct to consumer activities in North America, the UK and Germany via infomercial, online campaigns, radio and print media, which resulted in an increase in advertising, media buying, and other related selling and marketing expenses. Additionally we have increased the marketing activities of the XTRAC laser system in the US market.
Overall media buying and advertising expenses in the year ended December 31, 2013 were 32.0% of total revenues compared to 27.5% of total revenues in the year ended December 31, 2012. This percentage increase is due to the factors listed above as well as the change in mix of revenues particularly as a result of the decrease in revenues from our Japan distributor. These distributor revenues require substantially less sales and marketing costs than what is required in the direct channel. Direct to consumer revenues are 58.2% of total revenues for the year ended December 31, 2013 compared to 56.6% of total revenues for the year ended December 31, 2012. In addition, we added new initiatives to support our XTRAC therapy for psoriasis and vitiligo spending approximately $2,356.
General and Administrative Expenses
For the year ended December 31, 2014, general and administrative expenses increased to $35,711 from $26,750 for the year ended December 31, 2013 for the following reasons:
We have recorded $2,879 in costs related to the acquisition of LCA Vision.
We have recorded $1,365 in bank debt related costs and expenses.
We have had an increase in bad debt expenses related to both the Canada and Germany markets as well as an international distributor of approximately $3,680.
We have recorded $2,974 in costs related to the various litigations.

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For the year ended December 31, 2013, general and administrative expenses decreased to $26,750 from $27,330 for the year ended December 31, 2012 for the following reasons:
There was a decrease of $4,813 for the year ended December 31, 2013 in legal expense due to the completion of major litigation during 2012.
Offsetting the above decrease, there was an increase in bad debt expenses of $1,329 related to the increase in direct to consumer revenues and an international distributor.
Interest and Other Financing Expense, Net
Net interest and other financing expense for the year ended December 31, 2014 increased to $4,387, as compared to net interest and other financing income of $702 for the year ended December 31, 2013. The increase of $5,089 is due to an increase in interest expense of $2,969. The interest expense was related to the long term debt and the amortization of the related debt costs that was entered into in May 2014. During year, the entire related debt costs were written off as current period expense due to the restructuring of the long term debt. This does not include interest expense of $2,065 that was included as part of the loss on discontinued operations according to ASC Topic 205. The remaining change was due to currency fluctuation of the U.S. Dollar versus the New Israeli Shekel, the Euro, the GBP and the Australian Dollar. The functional currency of all U.S. members of the group, as well as Radiancy Ltd. (Israel), is the U.S. Dollar. The other foreign subsidiaries' functional currency is the each subsidiaries' respective local currency.
Net interest and other financing income for the year ended December 31, 2013 increased to $702, as compared to net interest and other financing expense of $351 for the year ended December 31, 2012. The increase of $1,053 is due to a decrease in interest expense of $399. The interest expense related to the term note that was assumed in the reverse merger. The remaining change was due to currency fluctuation of the U.S. Dollar versus the New Israeli Shekel, the Euro, the GBP and the Australian Dollar. The functional currency of all members of the group is the U.S. Dollar, except for Photo Therapeutics, Ltd, which has a functional currency of GBP and LK Technology, which has a functional currency of the Brazilian Real.
Taxes on Income, Net
For the year ended December 31, 2014, net taxes on income amounted to $36,312 as compared to $4,370 for the year ended December 31, 2013. The increase was mainly due to establishing valuation allowances of $40,803 on the net deferred tax assets as of December 31, 2014.
For the year ended December 31, 2013, net taxes on income amounted to $4,370 as compared to $4,438 for the year ended December 31, 2012. Partially offsetting the tax expense for the year ended December 31, 2012, we recorded a carryback of Radiancy, Inc.'s 2011 net operating loss to its 2010 tax return. The refund was received on February 28, 2013.
Net (Loss) Income
The factors discussed above resulted in a net loss, including discontinued operations, of $121,496 during the year ended December 31, 2014, as compared to net income of $18,377 during the year ended December 31, 2013. The factors discussed above resulted in a net income of $18,377 during the year ended December 31, 2013, as compared to $22,489 during the year ended December 31, 2012.
To supplement our consolidated financial statements presented elsewhere within this report,statements.

Recent Accounting Pronouncements Not Adopted Yet

In February 2016, the FASB issued ASU No. 2016-02, Leases. This guidance will require that lease arrangements longer than 12 months result in accordance with GAAP, management provides certain non-GAAP measuresan entity recognizing an asset and liability equal to the present value of the lease payments in the statement of financial performance. These non-GAAP measures include non-GAAP adjusted income.

Management's reference to these non-GAAP measures should be considered in addition to results prepared under current accounting standards, but are notposition. This guidance is effective for annual periods beginning after December 15, 2018, and interim periods therein. This standard requires a substitutemodified retrospective transition approach for nor superior to, GAAP measures. These non-GAAP measures are provided to enhance readers' overall understanding of our current financial performance and to provide further information for comparative purposes.
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Specifically, management believes the non-GAAP measures provide useful information to management and investors by isolating certain expenses, gains and losses that may not be indicative of our core operating results and business outlook. In addition, management believes non-GAAP measures enhance the comparability of results against prior periods. Reconciliation to the most directly comparable GAAP measure of all non-GAAP measures included in this report is as follows:
   For the Year ended December 31, 
  2014  2013  Change 
       
Net (loss) income (121,496) $18,377  (139,873)
             
Adjustments:            
Depreciation and amortization  6,912   6,119   793 
Interest expense, net  2,979   10   2,969 
Income tax expense  36,312   4,370   31,942 
             
EBITDA  (75,293)  28,876   (104,169)
             
Stock-based compensation expense  4,938   4,985   (47)
Acquisition costs  2,879   -   2,879 
Major litigation  2,974   -   2,974 
Extraordinary items, according to credit facility definition  2,812   -   2,812 
Loss from discontinued operations  15,155   -   15,155 
Loss from sale of discontinued operations  44,598   -   44,598 
             
Non-GAAP adjusted (loss) income (1,937) $33,861  (35,798)
Reconciliation to the most directly comparable GAAP measure of all non-GAAP measures included in this report is as follows:
   For the Year ended December 31, 
  2013  2012  Change 
       
Net income $18,377  $22,489  (4,112)
             
Adjustments:            
Depreciation and amortization  6,119   5,611   508 
Interest expense, net  10   398   (388)
Income tax expense  4,370   4,438   (68)
             
EBITDA  28,876   32,936   (4,060)
             
Stock-based compensation expense  4,985   6,197   (1,212)
             
Non-GAAP adjusted income $33,861  $39,133  (5,272)
Liquidity and Capital Resources 
At December 31, 2014, our current ratio was 1.24 compared to 2.46leases existing at, December 31, 2013. As of December 31, 2014 we had $25,537 of working capital compared to $83,058 as of December 31, 2013. Cash and cash equivalents were $10,605 as of December 31, 2014, as compared to $45,388 as of December 31, 2013. In addition, we had $87 and $14,113 in short term bank deposits as of December 31, 2014 and 2013, respectively.
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On May 12, 2014, weor entered into an $85 million senior secured credit facilities ("the Facilities") with JP Morgan Chase ("Chase") which included a $10 million revolving credit facility and a $75 million four-year term loan. The facilities were utilized to refinance the existing term debt with Chase, fund the acquisition of LCA and for working capital and other general corporate purposes.
Interest was initially determined at Eurodollar plus a margin between 3.25% and 4.50%. The margin is updated quarterly based on the then-current leverage ratio. The facilities are secured by a first priority security interest in and lien on all our assets. All current and future subsidiaries are guarantors on the facilities. There are financial covenants including; a maximum leverage covenant and a minimum fixed charge covenant, which we must maintain. These covenants will be determined quarterly based on a rolling past four quarters of financial data.
On August 4, 2014, we received a notice of default and a reservation of rights from Chase and engaged a third-party independent advisor to assist us in negotiating a longer term solution to the defaults. The parties had entered into an initial Forbearance Agreement (the "Initial Forbearance Agreement") on August 25, 2014. On November 4, 2014, we entered into an Amended and Restated Forbearance Agreement (the "Amended Forbearance Agreement") with the lenders that are parties to the Credit Agreement and with Chase, as Administrative Agent for the Lenders.
As of December 31, 2014, we continued to fail to meet both financial covenants and are in default of the credit facilities.
Effective February 28, 2015, we entered into an Second Amended and Restated Forbearance Agreement (the "Second Amended Forbearance Agreement") with the lenders (the "Lenders") that are parties to the Credit Agreement dated May 12, 2014, and with JP Morgan Chase, as Administrative Agent for the Lenders.
Pursuant to the terms of the Second Amended Forbearance Agreement, the Lenders have agreed to forbear from exercising their rights and remedies with respect to the Specified Events of Default from August 25, 2014 until April 1, 2016, or earlier if an event of default occurs (the "Forbearance Period"). Chase and the Lenders agreed that we shall not be obligated to pay the principal amounts set forth in Section 2.08(b) of the Credit Agreement for any date identified therein during the period beginning on February 28, 2015 and ending on the end of the Forbearance Period (the "Effective Period"), and that any failure to do so shall not constitute a default or event of default. Instead, the Lenders and the Company agreed that we would make prepayments against the Term Loan of $250,000 on the first business day of each month during the Forbearance Period, which will be applied in direct order of maturity. We also agreed that, on or before the fifth calendar day of each month, we would pay against the Term Loan $125,000 to the extent that the cash-on-hand exceeds $5 million, and 100% of the cash-on-hand in excess of $7 million, also to be applied to the Term Loan in inverse order of maturity.
Under the provisions of the Second Amended Forbearance Agreement, we will not have to comply with certain financial covenants contained in Section 6.11 of the Credit Agreement for the Forbearance Period, and that any failure to do so shall not constitute a default or event of default. However, we will have to meet certain minimum EBITDA targets (as defined in the forbearance agreement) for the quarters ending March 31, 2015, June 30, 2015, September 30, 2015 and December 31, 2015.
Pursuant to the Second Amended Forbearance Agreement, all loans under the Facilities shall, beginning November 1, 2014, bear interest at the CB Floating Rate (as defined in the Credit Agreement) plus 4.00%. Additionally, following the occurrence and continuance of any default or event of default (other than a Specified Event of Default), our obligations under the Facilities shall, at the option of Chase and the Lenders, bear interest at the rate of 2.00% plus the rate otherwise in effect.
We and our subsidiaries have also agreed not to pay in cash any compensation to the either our Chief Executive Officer or President that is based on a percentage of sales or another metric other than those officer's base salary, perquisites and standard benefits provided to or on behalf of those executives under the terms of their employment agreements. Those payments may be accrued or deferred and paid in cash only after, the repayment of the Facilities in full.
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We have agreed to provide, on or before May 29, 2015, a strategic business plan for the overall direction of the Company and our subsidiaries' businesses, including projected income statements, balance sheets, schedules of cash receipts and cash disbursements, payments and month-end balances, and detailed notes and assumptions, projected on a monthly basis through April 1, 2016. We have also agreed to provide quarterly updates to that plan by August 31, 2015, November 30, 2015 and February 29, 2016.
We continue to retain the services of both Getzler Henrich & Assoc. LLC, a third-party independent business advisor, as well as Canaccord Genuity, Inc., a banking and financial services company, and have also retained the services of Nomura Securities International, Inc., also a banking and financial services company. During the Forbearance Agreement, we and our advisors will continue to prepare and distribute offering memoranda and other marketing materials to prospective lenders with regard to a proposed credit facility for us, the proceeds of which would be in an amount sufficient to repay in full and in cash our remaining obligations under the Facilities, and to explore other strategic alternatives. The closing of any such refinancing or alternative arrangement would occur no later than the end of the Forbearance Period.
We have agreed to limit certain capital expenditures to $100,000 per quarter, except for those involving our XTRAC ®  or VTRAC ®  medical devices, and will not make investments or acquire any other interests in affiliated companies except as agreed to by the Lenders.
As consideration for the Lender's entry into the Second Amended Forbearance Agreement, we has agreed to pay the Lenders certain forbearance fees (the "Forbearance Fees"), which are earned on the last business day of each of the specified months: for May and June 2015, $750,000 each month; for July through September 2015, $1,000,000 each month; for October through December 2015, $1,250,000 each month; and for January through March 2016, $1,500,000 each month. However, should we complete a capital transaction acceptable to the Lenders that reduces the then-outstanding principal balance of the Term Loan to less than $10 million and repays all Forbearance Fees accrued and unpaid to that date, the monthly Forbearance Fee for the remainder of the Forbearance Period shall be earned and accrued in an amount that is 50% of the amount specified for each of the remaining months.  In addition, the $500,000 Forbearance Fee set forth in Section 4.10(b) of the Amended Forbearance Agreement remains due and payable to the Lenders on the earlier of the Expiration Date or the Termination Date of the Forbearance Period. All Forbearance Fees are considered earned and are included in the Obligations under the Credit Agreement.
The Second Amended Forbearance Agreement is also subject to customary covenants, including limitations on the incurrence of or payments on indebtedness to other persons or entities and requirements that we provide periodic financial information and information regarding the status of outstanding litigation involving us and our subsidiaries to the Lenders.
On December 12, 2014, we closed on a registered offering in which we sold an aggregate of 645,000 shares of our common stock at an offering price of $2.19 per share. The sale resulted in net proceeds of approximately $1.4 mmillion.
On April 27, 2012, we closed on a two-tranche registered offering in which we sold an aggregate of 3,023,432 shares of its common stock at an offering price of $13.23 per share. The sale resulted in net proceeds of approximately $37.8 million. The net proceeds will be used for general corporate purposes, including capital expenditures, continued product development, sales and marketing initiatives and working capital.
On August 18, 2012, the Board of Directors approved a stock repurchase program up to a maximum to $25 million. In August 2013, the Board of Directors authorized an additional $30 million share re-purchase program of its common shares in the open market over the next twelve months, at such times and prices as determined appropriate by our management in collaboration with the Board of Directors. To date, we have repurchased 2,987,413 shares at an average price of $13.98 per share for a total of $41,757. The shares were purchased with cash on hand. No additional share purchases were made during the year ended December 31, 2014, and through the date of this filing.
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initial application, with an option to use certain transition relief. Early adoption is permitted. We believeare currently evaluating the impact that the adoption of ASU 2016-02 will have on our existing balancesfinancial statements and related disclosures.

In November 2016, the FASB issued ASU 2016-18, Statement of Cash Flows (Topic 230): “Restricted Cash” (ASU 2016-18), which requires companies to include amounts generally described as restricted cash and restricted cash equivalents in cash and cash equivalents will be sufficient to satisfy our working capital needs, capital asset purchases, outstanding commitmentswhen reconciling beginning-of-period and other liquidity requirements associated with our existing operations throughend-of-period total amounts shown on the statement of cash flows. The amendments in this update are effective for public business entities for fiscal years beginning after December 15, 2017, and beyond the first quarter of 2016. However, thereinterim periods within those fiscal years. Early adoption is no guarantee that the Company will be able to enter into a refinancing or alternative arrangementpermitted, including adoption in a timely manner or under such terms as are acceptable to the Lenders. In the event that the Company is unable to enter into such an acceptable arrangement, or if, by the end of the Forbearance Period, the Company and its Lenders haveinterim period. This new guidance does not entered into another forbearance agreement or otherwise reached an agreement regarding the Credit Agreement and the Facilities, the Lenders have the right to declare all of the obligations under the Credit Agreement and Facilities due and payable, including principal and interest, as authorized by the Credit Agreement, and to enforce additional obligations under the Second Amended Forbearance Agreement. Such a result would have a material adverse effectimpact on our consolidated financial statements.

In May 2017, the CompanyFASB issued ASU 2017-09 guidance on changes to terms and its financial condition.

Net cash and cash equivalents used in operating activities was $24,171conditions of share-based payment awards. The amendment provides guidance about which changes to terms or conditions of a share-based payment award require an entity to apply modification accounting. The guidance will be effective for the fiscal year ended December 31, 2014 compared to cash provided by of $25,037 forbeginning on January 1, 2018, including interim periods within that year (early adoption is permitted). We are currently evaluating the year ended December 31, 2013. This decrease was mainly due to the net loss for the year ended December 31, 2014.
Net cash and cash equivalents provided by operating activities was $25,037 for the y ear ended December 31, 2013 compared to $24,996 for the year ended December 31, 2012.
Net cash and cash equivalents used in investing activities was $75,679 for the year ended December 31, 2014 compared to $2,448 for the year ended December 31, 2013. This was primarily due to the acquisition of LCA-Vision, net of cash received and the increase in the placement of lasers into service for the year ended December 31, 2014.
Net cash and cash equivalents used in investing activities was $2,448 for the year ended December 31, 2013 compared to $21,794 for the year ended December 31, 2012. This was primarily due to the increase in the placement of lasers into service for the year ended December 31, 2013 compared to the purchase of short term deposits of $18,000 for the year ended December 31, 2012.
When we retire a laser from service that is no longer useable, we write off the net book valuepotential effect of the laser, which is typically negligible. Over the last few years, such retirements of lasers from service have been immaterial.
Net cash and cash equivalents provided by financing activities was $65,653 for the year ended December 31, 2014 compared to net cash and cash equivalents used in financing activities of $21,672 for the year ended December 31, 2013. In the year ended December 31, 2014, we had proceeds from credit facilities of $75,000. This increase was offset, in part, to payments on credit facilities of $8,500 and notes payable and other debt of $838. In the year ended December 31, 2013, we had repurchased company stock for $31,029 and repayments of $623 for certain notes payable, which was partially offset by a draw on credit facility of $10,000.
Net cash and cash equivalents used in financing activities was $21,672 for the year ended December 31, 2013 compared to Net cash and cash equivalents provided by financing activities of $24,592 for the year ended December 31, 2012. In the year ended December 31, 2013, we had repurchased company stock for $31,029 and repayments of $623 for certain notes payable, which was partially offset by a draw on credit facility of $10,000. In the year ended December 31, 2012, we had proceeds from issuance of common stock, net of $37,514, which was partially offset by repayments of $2,000 on long-term debt and $465 for certain notes payable.
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Contractual Obligations
Set forth below is a summary of our current obligations as of December 31, 2014 to make future payments due by the period indicated below, excluding payables and accruals. We expect to be able to meet our obligations in the ordinary course. Operating lease and rental obligations are respectively for personal and real property which we use in our business. Included in the rental and operating lease obligations below are $17,916 related to LCA, which the Company sold on January 31, 2015.
  Payments due by period 
 
Contractual Obligations
 
Total
  Less than 1 year  
1 – 3 years
  
4 – 5 years
 
         
Credit facility obligations* $76,500  $38,732  $37,768  $- 
Rental and Operating lease obligations  19,744   6,532   13,211   - 
Notes payable  729   704   25   - 
     Total $96,973  $45,968  $51,004  $- 
*Potential increases to the credit facility obligations due to the forbearance agreement fees have not been included in the table.
Off-Balance Sheet Arrangements
At December 31, 2014, we had no off-balance sheet arrangements.
Impact of Inflation
We have not operated in a highly inflationary period, and we do not believe that inflation has had a material effectguidance on our revenues or expenses.consolidated financial statements.


ITEM 7A.QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK.

Item 7A.    Not applicable.Quantitative and Qualitative Disclosure about Market Risk

Foreign Exchange Risk
We are exposed to foreign currency exchange rate fluctuations related to the operation of our international subsidiaries. The Company's United Kingdom, PTL, subsidiary's main operating currency is pounds sterling. The Company's Brazilian, LK Technology, subsidiary's main operating currency is Brazilian Real. The Company's other foreign subsidiaries' functional currency is the respective local currency for each subsidiary, except Radiancy Ltd, At the end of each reporting period, revenue and expense of the foreign subsidiaries are converted into U.S. dollars using the average currency rate in effect for the period and assets and liabilities are converted into U.S. dollars using the exchange rate in effect at the end of the period.
The functional currency for our Israeli subsidiary, Radiancy, Ltd. is the US Dollar, but certain day-to-day transactions in Israel (for example, payment of salaries to Israeli employees) are transacted in New Israeli Shekels, therefore , we face some risk from fluctuations in the foreign exchange rates when accounting for these transactions. Additionally, we are exposed to foreign currency exchange rate fluctuations relating to payments we make to vendors and suppliers using foreign currencies. We currently do some hedging against the New Israeli Shekels. Fluctuations in exchange rates may impact our financial condition and results of operations.
See our Risk Factors regarding foreign currency exchange related risks.

Item 8.Financial Statements and Supplementary Data.
ITEM 8.FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA.

The financial statements required by this Item 8 are included in this Report and begin on page F-1.

Item 9.Changes in and Disagreements with Accountants on Accounting and Financial Disclosure
ITEM 9.CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE.

None.


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ITEM 9A.CONTROLS AND PROCEDURES.

Item 9A.    Controls and Procedures

Evaluation of Disclosure Controls and Procedures
Our management, with the participation of our Chief Executive Officer and Chief Financial Officer, has evaluated the effectiveness of the design and operation of our disclosure controls and procedures, (as such term is defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934 (the "Exchange Act")), as of December 31, 2014. Based on that evaluation, management has concluded that, as of such date, our disclosure controls and procedures were effective at the reasonable assurance level described below.

We maintain disclosure controls and procedures that are(as defined in Rule 13a-15(e) under the Exchange Act). Disclosure controls and procedures refer to controls and other procedures designed to ensure that information required to be disclosed by us in the reports that we file or submit under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in SECthe rules and forms of the SEC and that such information is accumulated and communicated to our management, including our Chief Executive Officerchief executive officer and Chief Financial Officer,chief financial officer, as appropriate, to allow timely decisions regarding required disclosure.

In designing

As required by Rule 13a-15(e) of the Exchange Act, our newly-appointed management has carried out an evaluation, with the participation and evaluatingunder the supervision of our Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and operation of our disclosure controls and procedures, as of December 31, 2017. Based upon, and as of the date of this evaluation, management recognizedhas determined that, despite the significant deficiency described below, our disclosure controls and procedures no matter how well conceived and operated, can provide only reasonable, not absolute, assurance that the objectives of the disclosure controls and procedures are met. Additionally, in designing disclosure controls and procedures, our management necessarily was required to apply its judgment in evaluating the cost-benefit relationship of possible disclosure controls and procedures. The design of any disclosure controls and procedures also is based in part upon certain assumptions about the likelihood of future events, and there can be no assurance that any design will succeed in achieving its stated goals under all potential future conditions.

Management'swere effective.

Management’s Annual Report on Internal Control over Financial Reporting

Our

Management is responsible for establishing and maintaining adequate internal control over financial reporting as defined in Rules 13a-15(f) and 15d-15(f) underfor the Exchange Act. Our management conducted an assessment of the effectiveness of the Company's internalCompany. Internal control over financial reporting based onrefers to the framework established inprocess designed by, or under the 2013 Internal Control-Integrated Framework issuedsupervision of, our principal executive officer and principal financial and accounting officer, and effected by the Committeeour board of Sponsoring Organizations of the Treadway Commission (COSO). Based on this assessment, ourdirectors, management has determined that the Company's internal control over financial reporting was effective as of December 31, 2014.

Fahn Kanne & Co. Grant Thornton Israel, our independent registered public accounting firm, has issued an attestation report on our internal control over financial reporting, as of December 31, 2014 and such report is included elsewhere in this Form 10-K.
Because of the inherent limitations in a cost-effective control system, no evaluation of internal control over financial reporting can provide absolute assurance that misstatements due to error or fraud will not occur or that all control issues and instances of fraud, if any, within our Company have been detected. Therefore, even those systems determined to be effective can provide only reasonable assurance with respect to financial statement preparation and presentation. Management does not expect that the Company's disclosure controls and procedures or its internal control over financial reporting will prevent or detect all errors and all fraud.
The design of any system of controls is based in part on certain assumptions about the likelihood of future events, and there can be no assurance that any design will succeed in achieving its stated goals under all potential future conditions. Projections of any evaluation of controls effectiveness to future periods are subject to risks. Over time, controls may become inadequate because of changes in conditions or deterioration in the degree of compliance with policies or procedures.
Changes in Internal Control over Financial Reporting
There has been no change in our internal control over financial reporting in our most recent fiscal quarter that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
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REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
Fahn Kanne & Co.
Head Office
Levinstein Tower
23 Menachem Begin Road
Tel-Aviv 66184, ISRAEL
P.O.B. 36172, 61361
T +972 3 7106666
F +972 3 7106660
www.gtfk.co.il
Board of Directors and Stockholders
   PhotoMedex, Inc.
We have audited the internal control over financial reporting of PhotoMedex, Inc. (a Nevada corporation) and Subsidiaries ("the Company") as of December 31, 2014, based on criteria established in the 2013 Internal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO). The Company's management is responsible for maintaining effective internal control over financial reporting and for its assessment of the effectiveness of internal control over financial reporting, included in the accompanying Management's Report on Internal Control over Financial Reporting. Our responsibility is to express an opinion on the Company's internal control over financial reporting based on our audit.
We conducted our audit in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all material respects. Our audit included obtaining an understanding of internal control over financial reporting, assessing the risk that a material weakness exists, testing and evaluating the design and operating effectiveness of internal control based on the assessed risk, and performing such other procedures as we considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion.
A company's internal control over financial reporting is a process designedpersonnel, to provide reasonable assurance regarding the reliability of our financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. A company's internal control over financial reportingGAAP, and includes those policies and procedures that (1) that:

(1)pertain to the maintenance of records that in reasonable detail accurately and fairly reflect the transactions and dispositions of our assets;

(2)provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with GAAP, and that our receipts and expenditures are being made only in accordance with the authorization of our management and directors; and

(3)provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use or disposition of our assets that could have a material effect on the financial statements.

As described above, our newly-appointed Chief Executive Officer and Chief Financial Officer have evaluated the maintenanceeffectiveness of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of the company are being made only in accordance with authorizations of management and directors of the company; and (3) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or disposition of the company's assets that could have a material effect on the financial statements.

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Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.
In our opinion, the Company maintained, in all material respects, effective internal control over financial reporting as of December 31, 2014, based on criteria2017. In making this evaluation, management used the framework established in the 2013 Internal Control—Control–l - Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission, or COSO. The COSO framework summarizes each of the components of a company’s internal control system, including (i) the control environment, (ii) risk assessment, (iii) control activities, (iv) information and communication, and (v) monitoring. Based on our evaluation, we determined that, as of December 31, 2017, our internal control over financial reporting was effective despite the significant deficiency described below.


During its evaluation, management discovered that certain controls were not performing as expected. We also have audited,classified that under-performance as a significant deficiency in accordance with theour internal controls. Under standards ofestablished by the Public Company Accounting Oversight Board, (United States),a significant deficiency is a deficiency, or a combination of deficiencies, in internal control over financial reporting that is less severe than a material weakness, yet important enough to merit attention by those responsible for oversight of our financial reporting. The review discovered that the consolidatedprocessing and approval for payment of certain payables was being handled by the same person, rather than one individual entering the payables and another approving them for payment. This deficiency arose in part because of a reduction in the size of our accounting staff that required staff members to assume additional duties. The new controls implemented by our new management now require an additional layer of approval prior to processing payments, along with two individuals to execute and approve payments made by us. Further, we have inserted more frequent reviews of payables entries and bank statements. Management believes the additional controls will provide another layer of review for these accounting processes and ensure the effectiveness of our disclosure controls and procedures.

Changes in Internal Controls over Financial Reporting

We regularly review our system of internal control over financial statementsreporting and make changes to our processes and systems to improve controls and increase efficiency, while ensuring that we maintain an effective internal control environment. Changes may include such activities as implementing new, more efficient systems, consolidating activities, and migrating processes.

There have been no changes in our internal control over financial reporting during the fourth quarter of fiscal year 2017 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

Our independent registered public accounting firm is not required to attest to the Company aseffectiveness of and for the year ended December 31, 2014 and our report dated March 16, 2015, expressed an unqualified opinion on thoseinternal control over financial statements.



/s/FAHN KANNE & CO. GRANT THORNTON ISRAEL

Tel-Aviv, Israel
March 16, 2015
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reporting since we are considered a smaller reporting company.

Item 9B.    Other Information
On March 10, 2015, each
ITEM 9B.OTHER INFORMATION.

We have no information to disclose that was required to be disclosed in a report on Form 8-K during fourth quarter of our two executives, Dr. Dolev Rafaeli and Mr. Dennis McGrath, entered into Amended and Restated Employment Agreements (the "Amended Agreements") with the Company which supersede their respective Amended and Restated Employment Agreements previously entered into on August 5, 2014

The March 2015 Amended Agreements were required by certain provisions contained in the Second Amended and Restated Forbearance Agreement between the Company and its Lenders. Under the Amended Agreements, all cash bonuses to Dr. Rafaeli and Mr. McGrath will be deferred until the Company's repayment of the outstanding Facilities under the Credit Agreement in accordance with the provisions of the Forbearance Agreement.
Under the cash bonus provisions of the Amended Agreements (and subject to the deferral described in the preceding paragraph), Dr. Rafaeli will receive quarterly cash bonuses equal to the greater of $300,000 per calendar quarter and 1% of the Company's U.S. GAAP sales per calendar quarter in excess of targets set by the Compensation Committee, and Mr. McGrath will receive an annual cash bonus offiscal year 2017 but was not less than $316,000 per year. All or a portion of such bonuses may be paid in shares of Company stock to the extent mutually agreed by the Board and the executive.
reported.

The Amended Agreements also clarify the executives' rights to resign due to "Good Reason" in the event of a breach of the Amended Agreements by the Company or for any reason during the 30-day period immediately following a Change of Control of the Company and to payment of deferred bonuses in connection with the termination of their employment.  

PART III

Item
ITEM 10.DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE.

Directors and Executive Officers and Corporate Governance

Our directors currently have terms which will end at our next annual meeting of the stockholders or until their successors are elected and qualify, subject to their prior death, resignation or removal. Officers serve at the discretion of the Board of Directors. There are no family relationships among any of

Following is information about our directors and executive officers. Members of our Board of Directors are encouraged to attend meetings of the Board of Directors and the Annual Meeting of Stockholders. The Board of Directors held twelve meetings and executed six unanimous written consents in lieu of a meeting in 2014.

The following sets forth certain biographical information concerning our current directors and our executive officers as of March 15, 2015.
the date of this proxy statement.

NAME AGE POSITION
NameVineet P. Bedi Position35 AgeChief Executive Officer
Lewis C. PellMatthew Stolzar Non-Executive 33Chief Financial Officer and Chief Investment Officer
Dr. Bob Froehlich64Chairman of the Board of Directors71
Yoav Ben-DrorRichard J. Leider Non-Executive Vice Chairman of the Board of Directors57 62
Dolev RafaeliChief Executive Officer and Director51
Dennis M. McGrath President, Chief Financial Officer and Director58
James W. Sight61 Director
Dr. Dolev Rafaeli 59
Stephen P. Connelly53 Director63
Trevor HarrisDirector (February 2014)Michael R. Stewart 60Director
Directors

Vineet P. Bedi has served as our Chief Executive Officer since January 2, 2018. Mr. Bedi has over 15 years of experience in real estate investing, private equity, capital markets and Executive Officers

Lewis C. Pellpublic securities investing. Mr. Bedi served as the Founder, Managing Partner and Chief Investment Officer of KRV Capital, LP, an alternative asset management firm investing in real estate and hard assets across the capital structure with a focus on liquid and illiquid deep value investment opportunities, from 2016 to 2018. Prior to founding KRV Capital, LP, Mr. Bedi was appointedthe Founder, Managing Partner and Chief Investment Officer of Booth Park Capital Management, LLC, an alternative asset management firm investing in real estate related securities, from 2013 to 2015. Previously, Mr. Bedi served as a Managing Director and Portfolio Manager at Guggenheim Partners from 2012 to 2013, where he managed an opportunistic portfolio in the public and private real estate markets. Prior to that, Mr. Bedi was a Principal and senior investment professional at High Rise Capital Management, LP, a multi-billion dollar opportunity fund investing in the public and private real estate markets, from 2005 to 2011. Mr. Bedi began his career in the investment banking and proprietary trading groups at Bank of America Merrill Lynch and has held senior positions with Carlson Capital, LP, Schonfeld Group Holdings and Booth Park Capital Management, LLC. Mr. Bedi serves as an Adjunct Associate Professor of Finance at the NYU-Stern School of Business. Mr. Bedi is a graduate of the NYU-Stern School of Business and is a CFA Charterholder.


Matthew Stolzar has served as our Chief Financial Officer and Chief Investment Officer since January 2, 2018. Mr. Stolzar has 11 years of experience in finance, including capital markets, real estate private equity and public securities investing. Mr. Stolzar was most recently Head of Research and a Managing Director at KRV Capital, LP, a dedicated real estate securities and hard assets opportunity fund investment adviser, where he focused on deep value investments. Mr. Stolzar worked at KRV from March 2016 to September 2017. Prior to that, he was Head of Research and a Senior Analyst at Pyrrho Capital Management, a global cross-capital structure event driven investment manager, where he focused on hard asset sectors including real estate, financials, energy and mining. Mr. Stolzar worked at Pyrrho from July 2012 to March 2016. Prior to Pyrrho, Mr. Stolzar was an Investment Professional at Och-Ziff Real Estate from August 2007 to December 2011, where he analyzed and executed real estate private equity and credit transactions across the residential, commercial and hospitality sectors. Mr. Stolzar began his career as an Investment Banking Analyst at Credit Suisse in the Real Estate Group. Mr. Stolzar received his B.A. with Honors in Economics and a Minor in Mathematics from Stanford University and is a CFA Charterholder.

Dr. Bob Froehlich has served as the Chairman of our Board of Directors since May 2017. Dr. Froehlich has amassed over 40 years of experience in and around Wall Street. He began his career in the public sector from 1975 until 1985, working as a Budget Analyst for the City of Dayton, Ohio, the Chief Financial Officer for Montgomery County, Ohio’s Water & Sewer District and the first City Manager for the City of Beavercreek, Ohio. In 1985, he transitioned to the private sector where he was unanimously electeda senior executive with Ernst & Whinney from 1985 to serve1989. From 1989 to 1997, Dr. Froehlich held several senior executive roles at Van Kampen Merritt which after its merger with American Capital became Van Kampen American Capital. In 2001, he was appointed Vice Chairman of Scudder Investments when Scudder Funds merged with Kemper Funds. In 2002, when Deutsche Bank acquired Scudder Investments, Dr. Froehlich was named Vice Chairman of Deutsche Asset Management, a role he held until he retired in 2009. He came out of retirement in 2009 to help rebrand Hartford Financial after its near financial collapse serving as Non-Executivea Senior Executive with The Hartford Mutual Funds. In 2012, he retired for the second time. Since his second retirement from Wall Street, Dr. Froehlich has begun a new chapter in his professional career by building a portfolio of boards spanning private, public, not-for-profit and mutual fund companies. From a private company perspective, on June 4, 2014, Dr. Froehlich became the Chairman of the Board, on December 12, 2011. Mr. Pell wasCEO, President & Owner of the Kane County Cougars Baseball Club, the Class “A” minor league affiliate of the Arizona Diamondbacks and a member of Radiancy's Boardthe Midwest League. He was a Co-Owner and Director since 1998. Mr. Pell has founded overJanuary 7, 2013. On August 2, 2016, Dr. Froehlich was appointed an Independent Director for Galen Robotics, Inc., a dozen successful medical technology companies duringspin-off from John Hopkins University, focusing on the past three decades. In 1979, he founded Pentax Precision Instruments, which was sold to Asahi Optical Co. in 1990. In 1983, he founded American Endoscopy Inc., which was sold to C.R. Bard, Inc. (BCR-NYSE) in 1986. In 1984, he founded Versaflex Inc., which was sold to Medtronic in 1988. In 1989, he founded Heart Technology Corp., which went public in the U.S. in 1992 and was sold to Boston Scientific Corp. (BSX-NYSE) in 1995. In 1991, he founded InStent Inc., which becamesurgical robotic microsurgery market. From a public company in 1995perspective, on October 3, 2014, Dr. Froehlich was appointed an Independent Director for AXAR Acquisition Corp. (formerly AR Capital Acquisition Corp.) (NASDAQ: AXAR), a special purpose acquisition corporation formed for the purpose of effecting a merger, capital stock exchange or similar business combinations. He serves as Chairman of the Compensation Committee and a member of the Audit Committee. In July 2014, Dr. Froehlich was sold to Medtronic in 1996. In 1994, he founded Influenceappointed an Independent Director and Audit Committee, Conflicts Committee and Nominating & Governance Committee member for NexPoint Capital, Inc., whicha publicly registered non-traded business development company. From a not-for-profit company perspective, Dr. Froehlich serves on the Board of Directors of The Midwest League of Professional Baseball Clubs, Inc., on the Board of Directors and as Chairman of the Board for Kane County Cougars Foundation, Inc., and as an Independent Trustee and Distribution Committee Chairman and Audit Committee, and Litigation Committee member for Highland Capital Mutual Funds, a major mutual fund company. Previously, from 2017 to 2018, Dr. Froehlich was soldappointed an Independent Director, Nominating & Corporate Governance Committee member and Audit Committee Chairman for First Capital Investment Corporation, a publicly registered non-traded business development company with an objective of investing primarily in small and middle market companies in the United States. From 2013 to American Medical Systems2016, Dr. Froehlich was an Independent Director and Audit Committee Chairman for ARC Healthcare Trust, Inc. in 1999. Working with Dr. Shlomo Ben-Haim, Mr. Pell founded Biosense Inc. in 1994,

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which was sold to Johnson & Johnson in 1997. He is currently chairman, a publicly registered non-traded real estate investment program and an investorIndependent Director and Lead Independent Director, Audit Committee Chairman and Conflicts Committee Chairman for ARC Realty Finance Trust, Inc., a numberpublicly registered non-traded real estate investment program. From 2012 to 2016, Dr. Froehlich was an Independent Director and Lead Independent Director, Audit Committee Chairman and Conflicts Committee Chairman for American Realty Capital Daily NAV Trust, Inc., a publicly registered nontraded real estate investment program. From 2013 to 2016, Dr. Froehlich was Lead Independent Trustee and Audit Committee Chairman for Realty Capital Income Funds. From 2014 to 2016, Dr. Froehlich was on the Advisory Board of private medical device companies.Directors for Internet Connectivity Group, Inc., a full service digital media firm focusing on point of sale strategies. Dr. Froehlich received his Ph.D. from California Coast University in 1979, a M.A. from Central Michigan University in 1978, a M.P.A. from the University of Dayton in 1976 and a B.A. from the University of Dayton in 1975. In 1992,2008, he foundedwas awarded an Honorary Doctorate of Commercial Sciences from the Board of Trustees of Central Michigan University. Dr. Froehlich was selected to serve on our Board because of his extensive finance experience and remains the chairmanhis experience serving as an independent director for public companies, including as audit committee chair.


Richard J. Leider has served as a member of Vision-Sciences, Inc. (VSCI-NASDAQ).our Board of Directors since May 2017. Mr. PellLeider has a B.S. in political science from Brooklyn College and over 20more than 25 years of experience in the medical technology industry.commercial real estate industry with active involvement in its sub-specialties of office, hospitality, investment, development, construction and strategic management. A hospitality veteran, Mr. PellLeider directed the repositioning, renovation and execution of the successful conversion of the Resort at Squaw Creek into a condominium hotel facility. Since March 2003, he has served as president of Paramount Hotels Inc. a California hotel management company. A principal and cofounder of Anvil Builders Inc., Mr. Leider has directed business development for that company since July 2010. From June 2005 to December 2008, he led the global real estate platform at Tano Capital, LLC and formerly directed the investment platform in Northern California on behalf of Buchanan Street. He was a managing director of global operations at Citadon, Inc., of San Francisco, a provider of Internet solutions for the real estate and construction industries, from June 2000 to December 2001. From 1996 to 2000, he was an executive director at DTZ Staubach Tie Leung in Hong Kong. While in Asia, Mr. Leider’s responsibilities included all aspects of the real estate life cycle, from advisory services to opportunistic institutional direct investment. Prior to his tenure with DTZ Staubach Tie Leung, Mr. Leider was a senior vice president at CBRE in San Francisco. Mr. Leider graduated from the University of California at Berkeley in 1981, earning a B.A. in Political Economies of Industrial Societies, and later studied at Worchester College at Oxford University. Mr. Leider serves on the Boards of Mercy Housing, American Cancer Society, Union Square Business Improvement District and its Public Policy Committee. He is a member of the Urban Land Institute, and CCIM Institute (Certified Commercial Investment Manager). Mr. Leider also serves as an independent board member of First Capital Real Estate Trust Incorporated. Mr. Leider was selected to serve on the Company's boardour Board because of his over thirty-years' experience in leadership rolestwenty-five years’ background in the medical devicecommercial real estate industry.

    Yoav Ben-Dror was appointed toDennis M. McGrath has served as a member of our Board of Directors since July 2009. He currently serves as the Executive Vice President and was electedChief Financial Officer of PAVmed, Inc. (Nasdaq: PAVM, PAVMW) since March 2017. Previously, from 2000 to serve2017, Mr. McGrath served in several senior level positions of our company, including from 2011 to 2017 as Non-Executivedirector, President, and Chief Financial Officer. Prior to our reverse merger with Radiancy, Inc. in December 2011, he also served as Chief Executive Officer from 2009 to 2011 and served as Vice Chairman on December 12, 2011. Dr. Ben-Dror wasPresident of Finance and Chief Financial Officer from 2000 to 2009. He received honors as a P.A.C.T. (Philadelphia Alliance for Capital and Technology) finalist for the chairman2011 Investment Deal of Radiancy's Board since 2006.the Year, award winner for the SmartCEO Magazine 2012 CEO of the Year for Turnaround Company, and finalist for the Ernst & Young 2013 Entrepreneur of the Year. He is an entrepreneur with more than 30 years ofhas extensive experience in mergers and acquisitions, both domestically and internationally, and particularly involving public company acquisitions, including Surgical Laser Technologies, Inc., (formerly, Nasdaq: SLTI), ProCyte Corporation (formerly, Nasdaq: PRCY), LCA Vision, Inc. (formerly, Nasdaq: LCAV) and Think New Ideas, Inc. (formerly, Nasdaq: THNK). Prior to joining our company, he served in several senior level positions of AnswerThink Consulting Group, Inc. (then, Nasdaq: ANSR, now, The Hackett Group, Nasdaq: HCKT), a business consulting and technology integration company, including from 1999 to 2000 as Chief Operating Officer of the Internet Practice, the largest division of AnswerThink Consulting Group, Inc., while concurrently during the merger of the companies, serving as the acting Chief Financial Officer of Think New Ideas, Inc. (then, Nasdaq: THNK, now, Nasdaq: HCKT), an interactive marketing services and business solutions company. Mr. McGrath also served from 1996 until 1999 as Chief Financial Officer, Executive Vice President and director of TriSpan, Inc., an internet commerce solutions and technology consulting company, which was acquired by AnswerThink Consulting Group, Inc. in 1999. During his tenure at Arthur Andersen & Co., where he began his career, he became a Certified Public Accountant in 1981, holds inactive licenses in Pennsylvania and New Jersey, and has a B.S., maxima cum laude, in accounting from LaSalle University. In addition to continuing as a director of PhotoMedex, he serves as the audit chair and a director of several medical devicesdevice companies, including DarioHealth Corp. (Nasdaq: DRIO), Noninvasive Medical Technologies, Inc. and financial innovations.Cagent Vascular, LLC, and as an advisor to the board of an orphan drug company, Palvella Therapeutics, LLC. Formerly from 2007 to 2009, Mr. McGrath served as a director of Embrella Cardiovascular, Inc. (sold to Edwards Lifesciences Corporation, NYSE: EW). He currentlyalso serves on the Board of Dagon Batey-Mamguroth Le-Israel Ltd (silo houses), Final Inc. (high-frequency financial algorithm technology), Fitango Inc. (social network), Neurotech Solutions Ltd. (human cognitionTrustees for Manor College and behavior with an emphasis on attention deficit/hyperactivity disorder (ADHD)), and Impact First Investments Ltd. (investment management firm that specializes in social investing). He is a director at Keren Shemesh Foundation for the Encouragement of Young Entrepreneurs (in association with YBI (Youth Business International), a foundation assisting young entrepreneurs in transforming an idea into a successful sustainable small business), a director at Hatnuah Hezrachit Hachadasha Ltd. (social activity), and a trustee at the Hecht-Zilzer Trust (charity). Dr. Ben Dror previously served on the Board of Cellcom Israel Ltd. (CEL-NYSE), Dubek Ltd. (tobacco), Magic Box Ltd. (financial algorithm technology) and Holon Institute of Technology (H.I.T.), and was a member of the Board of Trustees of the Holon Institute of Technology (H.I.T.). He was also involved with InStent Inc., Influence Medical Technologies Ltd. and Disc-O-Tech Medical Technologies Ltd. Dr. Ben Dror is a member of the Israel Bar and holds a Doctor of the Science of Jurisprudence (J.S.D.) from the School of Law (Boalt Hall), University of California, Berkeley. Dr. Ben-DrorVisitors for Taylor University. Mr. McGrath was selected to serve on the Company's boardour Board because of his extensive background30 years’ experience in the development and implementation of innovative business and financial entrepreneurship.marketing practices.


Dr. Dolev Rafaeliwas appointed has served as a member of our Board of Directors since December 2011. He previously served as our Chief Executive Officer and director infrom December 2011.2011 until May 2017. Dr. Rafaeli joined our subsidiary Radiancy in February 2006 as president and CEO. He has over 2329 years of experience managing international operations. Prior to joining Radiancy, Dr. Rafaeli served from 2004 to 2006 as president and CEO of the USR Group, a consumer electronics products manufacturer, managing operations in Israel, China, Hong Kong and the U.S. Between 2000 and 2004, Dr. Rafaeli founded and served as general manager of Orbotech Ltd. (ORBK-NASDAQ), an automated optical inspection capital equipment manufacturer for the electronics industry in China and Hong Kong, where he was instrumental in building these operations into a $100 million a year business. Between 1997 and 2000, Dr. Rafaeli served as CEO of USR Ltd., a global electronics contract manufacturing company providing design, supply chain and manufacturing services to dozens of clients in the communications, consumer and medical device fields. USR Ltd. employed approximately 1,000 individuals. Dr. Rafaeli previously served as director of operations and manager of the Arad manufacturing facility for Motorola in its Land Mobile Product Solutions division, manufacturing and distributing communications, consumer and other infrastructure electronics products in excess of $400 million annually. Dr. Rafaeli graduated with a B.Sc. in industrial engineering and management cum laude and a M.Sc. in operations management from the Technion-Israel Institute of Technology, and holds a Ph.D. in business management from Century University and an MBA (with distinction) from Cornell University. Dr. Rafaeli was selected to serve on the Company's boardour Board because of his over twenty-years'twenty five years of senior executive and board of directors’ experience with private and public multi-national companies and his vast mergers and acquisitions successful track record.

Michael R. Stewart has served as a member of our Board of Directors since May 17, 2017. Mr. Stewart is a seasoned executive with over 25 years of experience in consumerC-level positions and 36 total years’ experience in executive management, operations and finance. He brings a wealth of expertise with particular strength in operations, financial management, strategy, M&A, capital raise, FDA matters, medical reimbursement as well as sales, marketing, product development and international salesproduct launch. He has extensive U.S. and operations.

Dennis M. McGrath, upon completion of the mergerInternational market expertise and has significant experience with Radiancy, reassumed his role of Chief Financial Officer in additionpublic company board and SEC matters. Currently, Mr. Stewart operates as a private consultant to President and director of PhotoMedex, tomultiple companies which he was appointedstarted in July 2009.late 2016. He is working with companies from private start-up to mid-size public companies assisting them with major negotiations, new product and company launches, merger and acquisitions and capital raises. From 2014 through 2016, Mr. McGrath had previouslyStewart served as President, Chief Executive Officer and Director of publicly traded STRATA Skin Sciences, Inc. From 1990 to 2014, Mr. Stewart held the positions of CEO, COO and CFO and Vice President, finance and administration from January 2000 through June 2009. He has held several senior-level positions in prior endeavors, including, from February 1999 to January 2000, serving as the COO of Internet Practice, the largest division for AnswerThink Consulting Group, Inc., a company specializing in business consulting and technology integration. Concurrently, from August 1999 until January 2000, Mr. McGrath served as CFO of Think New Ideas, Inc., a company specializing in interactive marketing services and business solutions.at two publicly traded companies. In addition to his executive career and his non-independent board positions, Mr. Stewart has served as an independent public company director and as an advisor to the financial reporting responsibilities, he was responsible for the merger integrationboard of Think New Ideas, Inc.several private companies. Mr. Stewart obtained both his MBA in Finance and AnswerThink Consulting Group, Inc. Prior to that, from September 1996 to February 1999, Mr. McGrath was CFO and executive vice-president, operations of TriSpan, Inc., an internet commerce solutions and technology consulting company that was acquired by AnswerThink Consulting Group, Inc.
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his BS in 1999. Mr. McGrath is currently a director of Noninvasive Medical Technologies, Inc. and LabStyle, Inc. Mr. McGrath graduated with a B.S. in accountingAccounting from LaSalle University in 1979.Philadelphia. Mr. McGrathStewart was selected to serve on the Company's boardour Board because of his twenty year's36 years’ experience in the developmentexecutive management, operations and implementation of innovative business and marketing practices.
James W. Sightfinance. was appointed to our Board of Directors on May 26, 2010. Mr. Sight, an investor serving on the board of directors of various other public companies, has over 20 years of experience in corporate restructurings and financings. Within his experience Mr. Sight has been, since November 2007, a significant shareholder of Feldman Mall Properties, Inc., a real estate investment trust formerly listed on the New York Stock Exchange under the symbol FLMP, and has served in the office of the REIT's President; acted since 1998

Pursuant to the present as a consultant to LSB Industries (NYSE: LXU);Stock Grant Agreement, dated December 22, 2017, Dr. Dolev Rafaeli and from 1995 to 2006, was a large shareholder in Westmoreland Coal (AMEX: WLB), and was active on its board of directors in directing the reorganization of the company and its emergence from Chapter 11. Mr. Sight was selected to serve on the Company's board because of his twenty-years' experience in business operations and management.

Stephen P. Connelly was appointed to our Board of Directors on May 3, 2007. Mr. Connelly joined Viasys Healthcare, Inc., a medical technology and device company in August 2001 and served as President and Chief Operating Officer from November 2002 until August 2004. In addition, Mr. Connelly was formerly Senior Vice President and General Manager of the Americas as well as a member of the Executive Committee of Rhone Poulenc Rorer. Mr. Connelly's broad background includes over twenty-five years of experience in the planning, development and management of rapid-growth marketing-driven businesses in the medical device and pharmaceutical fields. Since 1999, Mr. Connelly has been an adjunct professor at St. Joseph's University, teaching international management and global strategy in the MBA program in the Haub School of Business. In addition, Mr. Connelly has a diverse and comprehensive business background, with expertise in such areas as strategic and tactical business development, joint ventures, mergers, acquisitions and corporate partnering, structuring and finance. Mr. Connelly is well-versed in every aspect of marketing, sales, general management, research and development of high-technology products and processes. Mr. Connelly possesses extensive international experience, having lived in Asia and having had operational P&L responsibility in many developed countries. Mr. Connelly was selected to serve on the Company's board because of his twenty-five years' background in the medical device industry and his experience in business development.
    Trevor Harris was appointed to our Board of Directors on February 27, 2014. Mr. Harris has been a faculty member of the Columbia Business School of Columbia University for more than 20 years, is former chair of the Accounting Division and has won numerous teaching awards. Currently he is The Arthur J. Samberg Professor of Professional Practice at Columbia and co-director of the Center for Excellence in Accounting and Security Analysis. Dr. Harris is a member of the Office of Financial Research's Financial Research Advisory Committee, the Financial Reporting Policy Committee of the American Accounting Association and the editorial board of The Journal of Applied Corporate Finance. A respected consultant on national and international finance, investment and valuation matters, for two decades Dr. Harris has worked with and advised numerous corporations, including Morgan Stanley, Salomon Brothers, TIAA/CREF, Citicorp and the New York Stock Exchange. He has held a number of leadership and management positions with U.S. and global organizations, including serving as managing director and vice chairman of client services at Morgan Stanley. He has numerous publications to his credit and has made presentations on national and international accounting, finance and valuation issues. He received a Master of Commerce and Bachelor of Commerce degrees, and his Certificate of Accountancy, from the University of Cape Town, South Africa, and a doctorate in Business Administration from the University of Washington in 1983. Dr. Harris was selected to serve on the Company's board because of his twenty years' experience and his background in national and international financial and accounting matters.
Katsumi Oneda was appointed to our Board of Directors on December 12, 2011; Mr. Oneda retiredDennis M. McGrath resigned from our Board of Directors effective July 31, 2014. Mr. Oneda co-founded Vision-Sciences Inc., served as its presidentupon certain circumstances described in the Stock Grant Agreement. See “See Item 1 “Business—Recent Developments—Payout Notes and CEO from October 1993Stock Grant Agreement” for details regarding these circumstances.

Our directors currently have terms which will end at our next annual meeting of the stockholders or until their successors are elected and qualify, subject to February 2003, and served as chairman from October 1993 to October 2005. He served astheir prior death, resignation or removal. Officers serve at the vice-chairmandiscretion of the Board of DirectorsDirectors.

Family Relationships

There are no family relationships among any of Vision-Sciences from May 1992 to October 1993, as honorary chairmanour officers or directors.

Involvement in Certain Legal Proceedings

To the best of our knowledge, none of our directors or executive officers has, during the past ten years:

been convicted in a criminal proceeding or been subject to a pending criminal proceeding (excluding traffic violations and other minor offences);

had any bankruptcy petition filed by or against the business or property of the person, or of any partnership, corporation or business association of which he was a general partner or executive officer, either at the time of the bankruptcy filing or within two years prior to that time;

been subject to any order, judgment, or decree, not subsequently reversed, suspended or vacated, of any court of competent jurisdiction or federal or state authority, permanently or temporarily enjoining, barring, suspending or otherwise limiting, his involvement in any type of business, securities, futures, commodities, investment, banking, savings and loan, or insurance activities, or to be associated with persons engaged in any such activity;

been found by a court of competent jurisdiction in a civil action or by the SEC or the Commodity Futures Trading Commission to have violated a federal or state securities or commodities law, and the judgment has not been reversed, suspended, or vacated;


been the subject of, or a party to, any federal or state judicial or administrative order, judgment, decree, or finding, not subsequently reversed, suspended or vacated (not including any settlement of a civil proceeding among private litigants), relating to an alleged violation of any federal or state securities or commodities law or regulation, any law or regulation respecting financial institutions or insurance companies including, but not limited to, a temporary or permanent injunction, order of disgorgement or restitution, civil money penalty or temporary or permanent cease-and-desist order, or removal or prohibition order, or any law or regulation prohibiting mail or wire fraud or fraud in connection with any business entity; or

been the subject of, or a party to, any sanction or order, not subsequently reversed, suspended or vacated, of any self-regulatory organization (as defined in Section 3(a)(26) of the Exchange Act (15 U.S.C. 78c(a)(26))), any registered entity (as defined in Section 1(a)(29) of the Commodity Exchange Act (7 U.S.C. 1(a)(29))), or any equivalent exchange, association, entity or organization that has disciplinary authority over its members or persons associated with a member.

Corporate Governance

Overview

Our Board of Directors from October 1991 to October 1993, and as the chairman of the Board of Directors from September 1990 to October 1991. He has been on the Board of Directors of Vision-Sciences since

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1987. Mr. Oneda graduated from Sangyo Noritsu College in 1964. He has over 20 years of experience in the medical technology industry. Mr. Oneda was selected to serve on the company's board of directors because of his twenty years' experience in the medical device industry.
With respect to the incumbent members of the Board of Directors, none of the members has, in the past 10 years, been subject to a federal or state judicial or administrative order, judgment, decree or finding, not subsequently reversed, suspended or vacated, relating to any legal proceedings, which include judicial or administrative proceedings resulting from involvement in mail or wire fraud or fraud in connection with any business entity or based on violations of federal or state securities, commodities, banking, or insurance laws and regulations, or any settlement to such actions, and any disciplinary sanction or order imposed by a stock, commodities or derivatives exchange other self-regulatory organization.
Board Leadership Structure
maintains charters for select committees. In accordance with the provisions of our Bylaws, the total number of directors who may serve onaddition, our Board of Directors has adopted a written set of corporate governance guidelines and a code of business conduct and ethics and a code of conduct for our chief executive and senior financial officers that generally formalize practices that we already had in place. To view the charters of our Audit, Compensation and Nominations and Corporate Governance Committees, code of ethics, corporate governance guidelines, and other documents, please visit our website atwww.fcglobalrealty.com, under the Corporate Governance section of the Investor Relations page.

Governance Structure

Our Board of Directors has chosen to appoint a separate Chairman who is currently set at a maximum of eight.

We choose to separate the position ofnot our Chief Executive Officer from that of our Chairman of the Board of Directors.Officer. Our Board of Directors has made this decision based on their belief that an independent Chairman of the Board can act as a balance to the Chief Executive Officer, who also serves as a non-independent director. Officer.

The Board of Directors also has provided for the post of Vice Chairman, who will fulfill the duties of the Chairman when circumstances preclude the Chairman from fulfilling the duties of the chairmanship.


Board’s Role in Risk Oversight

Our Board of Directors administers its risk oversight function as a whole by making risk oversight a matter of collective consideration. While management is responsible for identifying risks, our Board of Directors has charged the Audit Committee of the Board of Directors with evaluating financial and accounting risk, the Compensation Committee of the Board of Directors with evaluating risks associated with employees and compensation. Investor-related risks are usually addressed by the Board as a whole. We believe an independent Chairman of the Board adds an additional layer of insight to our Board of Directors'Directors’ risk oversight process.

Compensation, Nominations

Independent Directors

In considering and Corporate Governancemaking decisions as to the independence of each of the directors of the Company, the Board considered transactions and Audit Committees

Generalrelationships between the Company (and its subsidiaries) and each director (and each member of such director’s immediate family and any entity with which the director or family member has an affiliation such that the director or family member may have a material indirect interest in a transaction or relationship with such entity). Our Board of Directors maintains chartershas determined that the following directors are independent as defined in the applicable rules of the Nasdaq Stock Market: Dr. Bob Froehlich, Richard J. Leider and Michael R. Stewart.

Audit Committee

Our Board of Directors has established an Audit Committee to assist it in fulfilling its responsibilities for select committees. In addition,general oversight of the integrity of our consolidated financial statements, compliance with legal and regulatory requirements, the independent auditors’ qualifications and independence, the performance of our independent auditors and an internal audit function and risk assessment and risk management. The duties of our Audit Committee include:

appointing, evaluating and determining the compensation of our independent auditors;


reviewing and approving the scope of the annual audit, the audit fee and the financial statements;

reviewing disclosure controls and procedures, internal control over financial reporting, any internal audit function and corporate policies with respect to financial information;

reviewing other risks that may have a significant impact on our financial statements;

preparing the Audit Committee report for inclusion in the annual proxy statement;

establishing procedures for the receipt, retention and treatment of complaints regarding accounting and auditing matters;

approving all related party transactions, as defined by applicable Nasdaq Rules, to which the Company is a party; and

evaluating annually the Audit Committee charter.

The Audit Committee works closely with management as well as our independent auditors. The Audit Committee has the authority to obtain advice and assistance from, and receive appropriate funding from us for, outside legal, accounting or other advisors as the Audit Committee deems necessary to carry out its duties.

Our Board of Directors has adopted a written set of corporate governance guidelines and a code of business conduct and ethics and a code of conductcharter for our chief executive and senior financial officers that generally formalize practices that we already had in place. We have adopted a Code of Ethics on Interactions with Health Care Professionals, an Anti-Fraud Program and a policy for compliance with the Foreign Corrupt Practices Act. To view the charters of our Audit Compensation and Nominations and Corporate Governance Committees, Code of Ethics, corporate governance guidelines, codes of conduct and whistle blower policy, please visit our website at www.photomedex.com,under the Corporate Governance sectionCommittee. The members of the Investor Relations page (this website address is not intended to functionAudit Committee are Dr. Bob Froehlich, Richard J. Leider and Michael R. Stewart. Mr. Stewart serves as a hyperlink and the information contained on our website is not intended to be a partChair of this Report). In compliance with Nasdaq rules, the majority of our Board of Directors is comprised of independent directors. Audit Committee.

The Board of Directors determined in 2014 that except for Messrs. Rafaeli and McGrath, who are our Chief Executive Officer and Chief Financial Officer, respectively, all current memberseach member of the Audit Committee satisfies the independence and other composition requirements of the SEC and The Nasdaq Stock Market. Our Board has determined that Dr. Bob Froehlich and Michael R. Stewart both qualify as an “audit committee financial expert” under Item 407(d)(5) of Directors are independent underRegulation S-K and have the revised listing standards ofrequisite accounting or related financial expertise required by applicable Nasdaq rules.

Nasdaq.

Compensation Committee.    

Our Compensation Committee discharges the Board of Directors'Directors’ responsibilities relating to compensation of our Chief Executive Officer and other executive officers, produces an annual report on executive compensation for inclusion in our annual proxy statement and this Report and provides general oversight of compensation structure. Other specific duties and responsibilities of the Compensation Committee include:

reviewing and approving objectives relevant to executive officer compensation;

evaluating performance and recommending to the Board of Directors the compensation, including any incentive compensation, of our Chief Executive Officer and other executive officers in accordance with such objectives;
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reviewing employment agreements for executive officers;

recommending to the Board of Directors the compensation for our directors;

administering our equity compensation plans (except the Non-Employee Director Stock Option Plan) and other employee benefit plans;

evaluating human resources and compensation strategies, as needed; and

evaluating periodically the Compensation Committee charter.

Our Board of Directors has adopted a written charter for the Compensation Committee. The members of the Compensation Committee is currently composed of Messrs. Ben-Dror, Connellyare Richard J. Leider and Pell. Dr. Ben-DrorMichael R. Stewart. Mr. Leider serves as the ChairmanChair of the Compensation Committee. Our Board of Directors determined that each member of the Compensation Committee in 2014 satisfies the independence requirements of Nasdaq. The Compensation Committee held four formal meetings during 2014.Nasdaq Stock Market.


The Compensation Committee reviews executive compensation from time to time and reports to the Board of Directors, which makes all final decisions with respect to executive compensation. The Compensation Committee adheres to several guidelines in carrying out its responsibilities, including performance by the employees, our performance, enhancement of stockholder value, growth of new businesses and new markets and competitive levels of fixed and variable compensation. The report of the Compensation Committee for 2014 is presented below.

Nominations and Corporate Governance Committee.    

Our Board of Directors has established a Nominations and Corporate Governance Committee for the purpose of reviewing all Board of Director-recommended and stockholder-recommended nominees, determining each nominee'snominee’s qualifications and making a recommendation to the full Board of Directors as to which persons should be our Board of Directors'Directors’ nominees. Our Board of Directors has adopted a written charter for the Nominations and Corporate Governance Committee. The Nominations and Corporate Governance Committee is composed of Messrs. Sight and Oneda; Mr. Oneda resigned from the Board and its Committees effective July 31, 2014. Mr. Sight serves as the Chairman of the Nominations and Corporate Governance Committee. The Nominations and Corporate Governance Committee held two meeting during 2014 in conjunction with a meeting of the full Board of Directors.

The duties and responsibilities of the Nominations and Corporate Governance Committee include:

identifying and recommending to our Board of Directors individuals qualified to become members of our Board of Directors;

recommending to our Board of Directors the director nominees for the next annual meeting of stockholders;

recommending to our Board of Directors director committee assignments;

reviewing and evaluating succession planning for our Chief Executive Officer and other executive officers;

monitoring the independence of our directors;

developing and overseeing the corporate governance principles applicable to members of our Board of Directors, officers and employees;

reviewing and approving director compensation and administering the Non-Employee Director Plan;
monitoring the continuing education for our directors; and

evaluating annually the Nominations and Corporate Governance Committee charter.
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Our Board of Directors has adopted a written charter for the Nominations and Corporate Governance Committee. The members of the Nominations and Corporate Governance Committee considers these requirements when recommending nominees to our Boardare Dr. Bob Froehlich and Richard J. Leider. Dr. Froehlich serves as the Chair of Directors. the Nominations and Corporate Governance Committee.

Our Nominations and Corporate Governance Committee utilizes a variety of methods for identifying and evaluating nominees for our directors. Our Nominations and Corporate Governance Committee will regularly assess the appropriate size of our Board of Directors and whether any vacancies on the Board of Directors are expected due to retirement or other circumstances. When considering potential director nominees, the Nominations and Corporate Governance Committee also considers the candidate'scandidate’s character, judgment, diversity, age, skills, including financial literacy and experience in the context of the needs of PhotoMedexthe Company and of our existing directors. The Nominations and Corporate Governance Committee also seeks director nominees who are from diverse backgrounds and who possess a range of experiences as well as a reputation for integrity. The Nominations and Corporate Governance Committee considers all of these factors to ensure that our Board of Directors as a whole possesses a broad range of skills, knowledge and experience useful to the effective oversight and leadership of our company.

Our Nominations and Corporate Governance Committee does not have a specific policy with regard to the Company.

Audit Committee.    Ourconsideration of candidates recommended by stockholders, however any nominees proposed by our stockholders will be considered on the same basis as nominees proposed by the Board. If you or another stockholder want to submit a candidate for consideration to the Board, of Directors has established an Audit Committeeyou may submit your proposal to assist itour Corporate Counsel in fulfilling its responsibilities for general oversight ofaccordance with the integrity of our consolidated financial statements, compliance with legal and regulatory requirements, the independent auditors' qualifications and independence, the performance of our independent auditors and an internal audit function and risk assessment and risk management. The duties of our Audit Committee include:
appointing, evaluating and determining the compensation of our independent auditors;
reviewing and approving the scope of the annual audit, the audit fee and the financial statements;
reviewing disclosure controls and procedures, internal control over financial reporting, any internal audit function and corporate policies with respect to financial information;
reviewing other risks that may have a significant impact on our financial statements;
preparing the Audit Committee report for inclusion in the annual proxy statement;
establishing procedures for the receipt, retention and treatment of complaints regarding accounting and auditing matters;
approving all related party transactions, as defined by applicable Nasdaq Rules, to which the Company is a party; and
evaluating annually the Audit Committee charter.
The Audit Committee works closely with management as well as our independent auditors. The Audit Committee has the authority to obtain advice and assistance from, and receive appropriate funding from us for, outside legal, accounting or other advisors as the Audit Committee deems necessary to carry out its duties.
Our Board of Directors has adopted a written charter for the Audit Committee that meets the applicable standards of the Commission and Nasdaq. The members of the Audit Committee are Messrs. Ben-Dror, Connelly and Dr. Harris. Dr. Harris has served as the Chairman of the Audit Committee since April 1, 2014; Mr. Connelly served as the acting Chairman of the Audit Committee until that time. The Audit Committee meets regularly and held eight meetings during 2014.
The Board of Directors determined in 2014 that each member of the Audit Committee satisfies the independence and other composition requirements of the Securities and Exchange Commission (the "Commission") and Nasdaq. Our Board has determined that each member of the Audit Committee qualifies as an "audit committee financial expert" under Item 407(d)(5) of Regulation S-K and has the requisite accounting or related financial expertise required by applicable Nasdaq rules.
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stockholder communication procedures set forth below.


Stockholder Communications with the Board of Directors

Our Board of Directors has established a process for stockholders to communicate with the Board of Directors or with individual directors. Stockholders who wish to communicate with our Board of Directors or with individual directors should direct written correspondence to Michele Pupach, Corporate Counsel at mpupach@photomedex.com or to the following address (our principal executive offices):address: Board of Directors, c/o Corporate Secretary, 100 Lakeside2300 Computer Drive, Horsham,Building G, Willow Grove, Pennsylvania 19044.19090. Any such communication must contain:

a representation that the stockholder is a holder of record of our capital stock;

the name and address, as they appear on our books, of the stockholder sending such communication; and

the class and number of shares of our capital stock that are beneficially owned by such stockholder.

Ms. Pupach or the Corporate Secretary, as the case may be, will forward such communications to our Board of Directors or the specified individual director to whom the communication is directed unless such communication is unduly hostile, threatening, illegal or similarly inappropriate, in which case Ms. Pupach or the Corporate Secretary, as the case may be, has the authority to discard the communication or to take appropriate legal action regarding such communication.

Code of Ethics

We have adopted a Code of Ethics that applies to all of our employees, officers and directors. The Code of Ethics is available on our web site atwww.fcglobalrealty.com under the Corporate Governance section of the Investor Relations page. We intend to provide disclosure of any amendments or waivers of our Code of Ethics on our website within four business days following the date of the amendment or waiver.

Section 16(a) Beneficial Ownership Reporting Compliance

Section 16(a) of the Exchange Act requires our directors and executive officers and beneficial holders of more than 10% of our common stock to file with the CommissionSEC initial reports of ownership and reports of changes in ownership of our equity securities. As of March 16, 2015, weWe believe, based solely on a review of the copies of such reports furnished to us, and representations of these persons that no other reports were filed and that all reports needed to be filed have been filed for the year ended December 31, 2014.

2017,except as follows: Form 3 filed by Robert Froehlich; Form 3 filed by Richard Leider; Form 3 filed by Michael Stewart; Form 3 filed by Suneet Singal; Form 3 filed by Steven Johnson; Form 3 filed by Darrel Menthe; Form 3 filed by First Capital Real Estate Trust Inc.; Form 3 filed by First Capital Real Estate Operating Partnership, L.P.; Form 4 filed by Robert Froehlich on September 9, 2017; Form 4 filed by Robert Froehlich on September 14, 2017; Form 4 filed by Robert Froehlich on September 20, 2017; Form 4 filed by Robert Froehlich on November 24, 2017; Form 4 filed by Robert Froehlich on December 8, 2017; Form 4 filed by Dr. Yoav Ben Dror; Form 4 filed by Dr. Dolev Rafaeli; Form 4 filed by Dennis McGrath; and Form 3 filed by Opportunity Fund I-SS, LLC.

ITEM 11.EXECUTIVE COMPENSATION.

Item 11.    Executive Compensation

COMPENSATION DISCUSSION AND ANALYSIS
Introduction
ThisSummary Compensation Discussion and Analysis describes our compensation program and objectives for our Named Executive Officers for our fiscal year endingTable - Fiscal Years Ended December 31, 2014, or fiscal 2014. Our Named Executive Officers for fiscal 2014 were Dr. Dolev Rafaeli, our Chief Executive Officer,2017 and Dennis M. McGrath, our President and Chief Financial Officer.
2016

The Compensation Committee of our Board of Directors is responsible for reviewing and approving the annual compensation of our Named Executive Officers.  The Compensation Committee is composed solely of directors who are not our current or former employees, and each is independent under the revised listing standards of Nasdaq. Our Board of Directors has delegated to the Compensation Committee the responsibility to review and approve our compensation and benefits plans, programs and policies, including the compensation of our Chief Executive Officer and our President and Chief Financial Officer as well as middle-level management and other key employees. The Compensation Committee administersfollowing table sets forth information concerning all of our executive compensation programs, incentive compensation plans and equity-based plans and provides oversight for all of our other compensation and benefit programs.

The key components of the compensation program for our Named Executive Officers are base salary, bonus and long-term incentives, which for fiscal 2014 was granted to the Named Executive Officers in the form of stock options under our 2005 Equity Plan. These components are administered with the goal of providing total compensation that is competitive in the marketplace, recognizes meaningful differences in individual performance and offers the opportunity to earn superior rewards when merited by individual and corporate performance.
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Objectives of Compensation Program
The Compensation Committee governs and administers our compensation plans with the intent to support the achievement of our long-term strategic objectives, to enhance stockholder value, to attract, motivate and retain highly qualified employees by paying them competitively and rewarding them for their own success and ours. Included in this evaluation is an analysis whether the Company's incentive compensation arrangements, including short-term (annual cash incentive) and long-term (equity awards) components, encourage unnecessary or excessive risks. Although incentive compensation is discretionary, the Compensation Committee typically considers overall performance of the Company when granting cash incentive awards and considers several factors, including each Named Executive Officer's contributions to the growth of the Company for the benefit of the stockholders when granting incentive equity awards. We have no retirement plans or deferred compensation programs in effect for our Named Executive Officers, except for our 401(k) plan in which our Named Executive Officers are eligible to participate and is made generally available to all of our employees. We do not have a specific formula for allocating between cash and non-cash compensation which has been in the form of stock options and awards of restricted stock.
In orderawarded to, assess whether our compensation program is competitive and effective, the Compensation Committee relies on its own comparative review of peer companies. As an ongoing matter, the Compensation Committee does not regularly engage third-party consultants to advise on our compensation policies. Furthermore, our Compensation Committee does not delegate its responsibilities for reviewing and approving Named Executive Officer compensation.
What Our Compensation Program is Designed to Reward
The key components of the compensation program for our Named Executive Officers are base salary, bonus and long-term incentives under the 2005 Equity Plan. These components are administered with the goal of providing total compensation that is competitive in the marketplace, recognizes meaningful differences in individual performance and offers the opportunity to earn superior rewards when meritedearned by individual and corporate performance.
Stock price performance has not been a factor in determining annual compensation insofar as the price of our common stock is subject to a number of factors outside of our control. We have endeavored through grants of stock options to our Named Executive Officers to incentivize individual and team performance by providing a meaningful stake in us that links their compensation to our overall success.
Elements of Company's Compensation Plan and How Each Element Relates to Objectives
There are three primary elements in the compensation package of our executive officers: base salary, bonus and long-term incentives. Compensation payable in the event of the termination of an executive's employment with the Company is a secondary but material element in the package.
Base Salaries.    Base salaries for our Named Executive Officers are designed to provide a base pay opportunity that is appropriately competitive within the marketplace. As an officer's level of responsibility increases, a greater proportion of his or her total compensation will be dependent on our financial performance and stock price appreciation rather than base salary. Adjustments to each individual's base salary are made in connection with annual performance reviews and an assessment of market competitiveness. In fiscal 2014paid to the base salaries increased to Dr. Rafaeli and Mr. McGrath ($495,000 and $395,000, respectively).
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Bonus.    Generally, at the outset of a fiscal year, the Compensation Committee establishes a bonus programnamed persons for our Named Executive Officers and other managers and key employees eligible to participateservices rendered in the program. The program is generally based on a financial plan for the fiscal year and other business factors, and certain management objectives that could be updated throughout the year to address and incentivize management relating to changing macro-economic, environmental and business issues. The amount of bonus, if any, hinges on corporate performance, financial condition, and on the performance against management objectives of the participant in the program. A program will typically allow partial or discretionary awards based on an evaluation of the relevant factors. Provision for bonus expense is typically made over the course of a fiscal year. The provision becomes fixed, based on the final review of the Compensation Committee, which is usually made after the financial results of the fiscal year have been reviewed by our independent accountants.

On January 25, 2014, the Board of Directors approved and adopted a 2014 annual bonus plan for employees, including Mr. McGrath. The 2014 bonus plan includes performance incentives for achievement of the corporate financial goals that are designed to motivate, retain and reward our employees based upon the achievement of corporate revenue and profitability objectives, as well as individual objectives in certain cases. The targeted incentive compensation and the revenue and profitability goals for each employee were established by the Compensation Committee at the outset of the year. Furthermore, updated objectives for Mr. McGrath were established by the Compensation Committee and the Board of Directors that were directly related to the Mr. McGrath's management of the Companies banking relationships and debt compliance tasks. At year-end and upon compilation of the financial results, the Compensation Committee met to review the Company's results compared with plan goals and management objectives and to determine the level of performance incentive awards to be paid based upon the measurement of attainment of all quantitative and qualitative goals.
Mr. McGrath's target bonus under the 2014 bonus plan was 80% of his salary based on the established goals as set out by the board of directors at the beginning of the year, as well as updated individual goals related to the effective management of banking relationships and debt compliance tasks. Actual achievement of the Company's management objectives was met, resulting in a bonus of $316,000, or 80% of salary.

Pursuant to Amended and Restated Employment Agreements dated March 10, 2015, Dr. Rafaeli and Mr. McGrath have been guaranteed certain minimum bonus amountscapacities during the term of their employment agreements, as described in Item 9B above and "Overview of Executive Employment Agreements and Option Awards," below.
Long-Term Incentives.    Grants of stock options and restricted stock awards under our employee stock plans are designed to provide our Named Executive Officers andnoted periods. No other managers and key employees with an opportunity to share, along with stockholders, in our long-term performance. Stock option grants or restricted stock awards are generally made annually to all Named Executive Officers, with additional grants being made following a significant change in job responsibility, scope or title or a significant achievement. The size of the grant to each Named Executive Officer is set by the Compensation Committee at a level that is intended to create a meaningful opportunity for stock ownership based upon several factors, including the individual's current position with us, the individual's personal performance in recent periods and his or her potential for future responsibility and promotion over the option term, but the Compensation Committee has the flexibility to make adjustments to those factors at its discretion. The Compensation Committee also takes into account the number of unvested stock options and restricted stock awards held by the Named Executive Officer in order to maintain an appropriate level of equity incentive for that individual. The relevant weight given to each of these factors varies from individual to individual.
We generally grant stock options with a five-year vesting schedule and 10 year term from the date of grant. The exercise price of options granted is at no less than 100% of the fair market value of the underlying stock on the date of grant. The options granted to Named Executive Officers as a rule have provisions by which vesting and exercisability are accelerated in the event of a change of control or a termination of employment initiated by us other than for cause. Such provisions are found in Dr. Rafaeli's and Mr. McGrath's employment agreements.
Similar criteria are applied in making awards of restricted shares of our common stock under the 2005 Equity Plan, but in the case of restricted stock, we base the vesting schedule of the restricted stock on the price performance of our common stock. Such awards generally carry a three-or-four year vesting schedule.
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Compensation on Termination of Employment or Change of Control.  We have employment agreements with Dr. Rafaeli and Mr. McGrath. Each of these agreements provides for severance upon termination of employment, whether in context of a change of control or not. See "Potential Payments on Termination of Employment or Change of Control" below.
Perquisites. We provide our Named Executive Officers with certain perquisites that we do not consider to be a significant part of their compensation. Under their employment agreements, we provide Dr. Rafaeli and Mr. McGrath with an automobile allowance of $1,000 per month. In addition, we provide Dr. Rafaeli with, and pay all expenses for, a telephone for his residence and he is eligible to receive the equivalent of economy round trip airfare tickets for all of his family members for anexecutive officers received total annual home leave between the US and Israel.
The Company pays the premiums for supplementary life insurance policies for both Dr. Rafaeli and Mr. McGrath. Both also receive a matching contribution from the Company to their 401(k) under the Company's 401(k) Plan which is available to all employees.
How Amounts Were Selected for Each Element of an Executive's Compensation
Each executive's current and prior compensation is considered in setting future compensation. In addition, the Compensation Committee reviews from time to time the compensation practices of other companies, particularly our peer companies. To some extent, our compensation plan is based on the market and the companies we compete against for executives. Base salary and the long-term incentives are not set with reference to a formula.
An executive's target bonus amount is set by an executive's employment agreement, which was negotiated at arm's length. A target bonus, or a portion thereof, is earned, based on fulfillment of conditions, which are set by the Compensation Committee at the outset of a fiscal year.
As a general rule, options and restricted stock awards are made after the financial results for the prior year have been audited and reported to our Board of Directors. Grants and awards are valued, and exercise prices are set, as of the date the grant or award is made. Exceptions to the general rule may arise for grants made to recognize a promotion or to address the effect of expiring options. The Compensation Committee may elect to defer a grant until after the Company has made public disclosure of its financial results, typically in a conference call on earnings. In such a case, the exercise price is set at the higher of the closing price on the approval date or the fixed grant date. In these deliberations, the Compensation Committee does not delegate any related function, unless to the Board of Directors as a whole, and the grants or awards made to the Named Executive Officers are valued under the same measurement standards as grants made to other grantees.
For fiscal 2014, our Compensation Committee granted restricted stock awards of our common stock of 225,000 and 165,000 to Dr. Rafaeli and Mr. McGrath, respectively. The stock has a par value of $0.01. These ownership interests in our Company are intended to incentivize our Named Executive Officers and align their interests with those of our stockholders. The restricted stock will vest and become exercisable in three equal installments on each of the first three anniversaries of the date of grant subject to the individuals continued employment with the Company, with accelerated vesting upon a change in control.
Accounting and Tax Considerations
We have adopted accounting standard, FASB ASC Topic 718 under which, we are required to value stock options granted and restricted stock awarded.
Under Section 162(m) of the Internal Revenue Code of 1986, as amended, or the Code, there is a limit placed on tax deductions of any publicly-held corporation for individual compensation to certain executives of such corporation (other than its chief financial officer) exceeding $1,000,000 in any taxable year, unless the compensation is performance-based. Compensation resulting from options is indexed as performance-based. To the extent consistent with the objectives of our compensation program, we intend to maximize the deductibility of compensation for tax purposes. The Compensation Committee may however, decide to exceed the tax deductible limits established under Section 162(m) of the Code, when such a decision appears to be warranted based upon competitive and other factors.
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Overview of Executive Employment Agreements and Option Awards
Employment Agreement with Dolev Rafaeli.    We are party to an employment agreement with Dolev Rafaeli, pursuant to which he serves as the Chief Executive Officer of PhotoMedex and the Chief Executive Officer and President of Radiancy. The initial employment agreement had a term of three years that commenced on December 13, 2011, the date of the closing of our merger with Radiancy. The Company and Dr. Rafaeli have entered into an Amended and Restated Employment Agreement, which has a term of four years that commenced on August 5, 2014 and ends on December 31, 2018. The Agreement will automatically terminate on December 18, 2018 unless the parties reach a written accord upon an extension or renewal of the Employment Agreement. Under the employment agreement, Dr. Rafaeli's salary is $495,000 per annum. In addition, Dr. Rafaeli is entitled to a bonus equal to 1% of the Company's sales (calculated as 1% of recognized U.S. GAAP sales reported in our consolidated quarterly financial reports presented to our Board of Directors), which bonus, when combined with all other applicable employee remuneration under I.R.C. Section 162(m)(4) from the Company may not exceed a $1,000,000 annual threshold. Such bonus will be paid quarterly. The Company stockholders approved that Dr. Rafaeli shall be entitled to an additional quarterly cash bonus equal to 1% of the sales of the Company in excess of such target threshold amount as the Compensation Committee shall determine (the "Second-Tier Bonus"). Following the end of each quarterly performance period, the Compensation Committee shall determine the Second-Tier Bonus for that quarter by calculating 1% of the Company's U.S. GAAP sales in excess of the threshold amount. Upon the termination of Dr. Rafaeli's employment by PhotoMedex without cause or by Dr. Rafaeli for good reason, he will be entitled to severance benefits as described in the section below entitled "Potential Payments on Termination of Employment or Change of Control".
Employment Agreement with Dennis M. McGrath.    We are party to an employment agreement with Dennis M. McGrath pursuant to which he serves as our President and Chief Financial Officer. The employment agreement had an initial term of three years that commenced on December 13, 2011, the date of the closing of our merger with Radiancy. The Company and Mr. McGrath have entered into an Amended and Restated Employment Agreement, which has a term of four years that commenced on August 5, 2014 and ends on December 31, 2018. The Agreement will automatically terminate on December 18, 2018 unless the parties reach a written accord upon an extension or renewal of the Employment Agreement. Mr. McGrath's 2014 annual base salary under his employment agreement is $395,000 and he is eligible to receive an annual bonus of up to 80% of his base salary based on the attainment of individual and corporate goals determined and set by our Board of Directors. In addition, he is entitled to participate in the long-term equity incentive programs established by the Company for its senior level executives generally commensurate with his position. The severance arrangements contained in Mr. McGrath's employment agreement are summarized in the section below entitled "Potential Payments upon Termination of Employment or Change in Control."
Under the Second Amended Forbearance Agreement, commencing on February 28, 2015, the Company and its subsidiaries have agreed not to pay in cash any compensation to the either Mr. Rafaeli or Mr. McGrath that is based on a percentage of sales or another metric other than those officer's base salary, perquisites and standard benefits provided to or on behalf of those executives under the terms of their employment agreements. Those payments may be accrued or deferred and paid in cash only after the repayment of the Facilities in full. As a result of these requirements, Mr. Rafaeli and Mr. McGrath entered into Amended and Restated Employment Agreements dated March 10, 2015 which will affect future payments for bonuses and severance and are described in Item 9B above. Under the cash bonus provisions of the Amended Agreements and subject to the deferral described above, Dr. Rafaeli will receive quarterly cash bonuses equal to the greater of $300,000 per calendar quarter and 1% of the Company's U.S. GAAP sales per calendar quarter in excess of targets set by the Compensation Committee, and Mr. McGrath will receive an annual cash bonus of not less than $316,000 per year. All or a portion of such bonuses may be paid in shares of Company stock to the extent mutually agreed by the Board and the executive.

SUMMARY COMPENSATION TABLE
The following table includes information for the years ended December 31, 2014, 2013 and 2012 concerning compensation for our Named Executive Officers.
Name and Principal PositionYear
Salary ($)
Non-Equity Incentive Plan Compensation ($) (1)
Stock Awards ($) (2)
Option Awards ($) (2)
All Other Compensation ($) (3)
Total ($)
        
Dolev Rafaeli, Chief Executive Officer2014468,0002,106,970702,000019,1523,296,122
2013450,0002,246,6400451,34535,6733,183,658
2012450,0002,206,98201,106,00040,5493,803,531
        
Dennis M. McGrath, President and Chief Financial Officer2014353,000316,000514,800022,7351,206,535
2013337,500234,0000332,57017,642921,712
 2012325,000234,0000711,00018,4871,288,487

$100,000.

Name and Principal Position Year  

Salary

($)

  

Stock Awards

($) (1) 

  Non-Equity Incentive Plan Compensation
($) (2)
  All Other Compensation
($) (3)
  

Total

($)

 

Suneet Singal,

  2017   67,500   0   910,000   0   977,500 
Former Chief Executive Officer(4)  2016   0   0   0   0   0 

Stephen Johnson,

  2017   182,308   0   0   0   182,308 
Former Chief Financial Officer(5)  2016   0   0   0   0   0 

Dr. Dolev Rafaeli,

  2017   3,260,307   0   0   

111,758

   

3,372,065

 
Former Chief Executive Officer(6)  2016   495,000   71,719   1,200,000   46,347   1,813,066 

Dennis M. McGrath,

  2017   970,284   0   0   

58,698

   

1,028,983

 
Former Chief Financial Officer(6)  2016   395,000   52,594   316,000   45,156   808,750 

 (1)"Non-Equity Incentive Plan Compensation" in the foregoing table is the bonus earned in 2014, 2013 and 2012, even though such bonus may have been paid in a subsequent period.
 (2)(1)The amounts shown for option awards, restricted stock awards and stock purchase rights relate to shares granted under our Amended and Restated 2005 Equity Compensation Plan. These amounts are equal to the aggregate grant-date fair value with respect to the awards made in 2014, 2013 and 2012,2016, computed in accordance with FASB ASC Topic 718 (formerly SFAS 123R), before amortization and without giving effect to estimated forfeitures. For information regarding


(2)The amounts shown for Dr. Rafaeli and Dennis M. McGrath relate to the numberbonus earned in 2016, even though such bonus may have been paid in a subsequent period. Dr. Rafaeli’s bonus of shares subject$1,200,000 and Mr. McGrath’s bonus of $316,000 remained accrued but unpaid for 2016. The amount shown for Suneet Singal represents the grant of restricted stock pursuant to 2014 awards, other features of those awardsa separation agreement, dated December 22, 2017, between us and Mr. Singal. This amount is equal to the aggregate grant-date fair value ofwith respect to the awards, see the Grants of Plan-Based Awards Table below.award made in 2017, computed in accordance with FASB ASC Topic 718 (formerly SFAS 123R).

(3)"All Other Compensation"Compensation” includes car allowance ($1,000 per month),allowances, premiums for supplementary life and/or disability insurance, of $8,088 and matching 401(k)401 (k) plan contributions, interest payments on payout notes issued to Dr. Rafeali and Mr. McGrath, and director fees paid or earned to Dr. Rafaeli and Mr McGrath after such persons resigned as executive officers of $2,647the Company.

(4)Mr. Singal served as our Chief Executive Officer from May 17, 2017 until January 2, 2018. Under Mr. Singal’s employment agreement, he was entitled to an annual base salary of $250,000, as well as bonuses and other equity compensation as determined by our Compensation Committee. On October 11, 2017, we entered into an amended a restated employment agreement with Mr. Singal. Under this agreement, Mr. Singal was entitled to a base salary of $250,000 per annum, payable in accordance with our normal payroll practices, provided however, that the base salary would accrue, and not be paid, until (i) the 20% Unsecured Convertible Promissory Note issued to the Contributor by our company on July 25, 2017 had been repaid in full and (ii) Mr. Singal began working for our company on a full-time basis. In connection with Mr. Singal’s resignation, on December 22, 2017, we entered into a separation agreement with Mr. Singal, pursuant to which Mr. Singal agreed to resign and we agreed to issue to Mr. Singal 1,000,000 shares of our common stock, 333,333 shares of which vested immediately, 333,333 shares of which will vest upon the first anniversary of the separation agreement, and 333,334 shares of which will vest upon the second anniversary of the separation agreement. The parties agreed that the issuance of such shares is in lieu of any other payment that Mr. Singal may already be entitled to receive under his employment agreement.

(5)Mr. Johnson served as our Chief Financial Officer from May 17, 2017 until January 2, 2018. Under Mr. Johnson’s employment agreement, he was entitled to an annual base salary of $300,000, as well as bonuses and other equity compensation as determined by our Compensation Committee. In connection with Mr. Johnson resignation, on December 22, 2017, we entered into a separation agreement with Mr. Johnson, pursuant to which Mr. Johnson agreed to resign and we agreed to pay to Mr. Johnson $405,432.70 in twelve (12) installments. We also agreed to pay for the health (medical, dental and/or vision) insurance policies for Mr. McGrath. For Dr. Rafaeli it includes matching 401(k) plan contributionsJohnson and his family for a period of twelve (12) months. We made the initial payment for Mr. Johnson’s separation and health benefits on January 8, 2017. On February 12, 2018, we entered into an amended and restated separation agreement with Mr. Johnson, pursuant to which we agreed to pay Mr. Johnson $122,500.64 in eleven installments as follows: the first six installments of $10,000, the following four installments of $12,500, and premiums for supplementary lifea final installment of $12,500.64. The first payment was made on February 15, 2018 and subsequent payments are to be made on or before the 15th day of each succeeding month, with the final installment to be paid on or before December 15, 2018. We also agreed to provide a health (medical, dental and/or disabilityvision) insurance of $6,652.
 (4)The 2013 "Non-Equity Inventive Plan Compensation"reimbursement payment for Mr. McGrath includedJohnson and his family, for a period of eleven (11) months, in the agreed upon amount of $3,025 per month. In addition, we agreed to issue to Mr. Johnson 271,000 shares of common stock, which will be issued six months after the date of the amended and restated separation agreement. The foregoing amounts are in lieu of any other payment of $39,000 paid pursuantthat Mr. Johnson may already be entitled to discretion exercised by the Compensation Committeereceive under that incentive plan.his employment agreement.

Potential Payments on Termination of Employment or Change of Control
Potential payments to our Named Executive Officers on termination of employment or upon a change of control of the Company are governed by their respective employment agreements and by the terms of their option agreements and restricted stock agreements or plan document.
104


Pursuant to the terms of their employment agreements, as of December 31, 2014, should (1) the Company terminate Dr, Rafaeli's or Mr. McGrath's employment without cause, (2) Dr. Rafaeli or Mr. McGrath resign for good reason or (3) the Company fail to renew the applicable employment agreement (in each instance, whether in the context of a change in control or otherwise), then the affected individual would become entitled to the following benefits upon his delivery of an effective release to the Company:

(i)(6)Continued payment of hisDr. Rafaeli resigned as our Chief Executive Officer on May 17, 2017. Under Dr. Rafaeli’s employment agreement, he was entitled to an annual base salary of $495,000, certain bonuses based on success in effect atsales, as well other equity compensation as determined by our Compensation Committee. In connection with Dr. Rafaeli’s resignation, we and Dr. Rafaeli agreed to convert all compensation due under his employment agreement into a secured convertible payout note to be issued following stockholder approval. On October 12, 2017, we issued the timepayout note in the principal amount of such termination$3,133,934 to Dr. Rafaeli. The payout note was due on October 12, 2018, carried a ten percent (10%) interest rate, payable monthly in arrears commencing on December 1, 2017, and was secured by a security interest in all of our assets. On December 22, 2017, we entered into a Stock Grant Agreement with Dr. Rafaeli and certain other note holders to (i) cause the early conversion of the payout note into 3,134,876 shares of our common stock, (ii) effectuate the release of all security interests associated with the payout note, (iii) provide for the remainderissuance of 1,034,509 additional shares of common stock as consideration for the termvarious agreements of Dr. Rafaeli contained in the agreement, payable in installments in accordance with the Company's payroll practices basedStock Grant Agreement, (iv) provide for twelve (12) monthly payments of $21,328.16 on the termsfirst of the agreement;
(ii)
For Dr. Rafaeli – continued payment of his First Tier  and Second Tier Bonuses, for the remainder of the term of the agreement; should Dr. Rafaeli no longer be deemed a 'covered employee' under the provisions of I.R.C. Section 162(m)(4), then the limitationeach month commencing on the amount of the First Tier Bonus shall not apply; and a pro-rated annual bonus for the year inJanuary 1, 2018, which such termination occurs;
For Mr. McGrath - a bonus for each fiscal year remaining in the term of the Agreement, at a rate that is not less than the highest annual bonus paid during any of the preceding years covered by the agreement or the prior employment agreement (but prorated for any partial fiscal year during the remaining term of the agreement, payable at the same time other employees of the Companyamounts are paid pursuant to the terms of the Company's annual bonus plan, but not later than March 15 of the year following the end of the fiscal year to which the bonus relates;.;
(iii)continued medical and dental coverage for himself and his eligible dependents for eighteen months following the date of termination or resignation, provided a timely election is made under COBRA provisions;
(iv)A monthly cash payment for the remainder of the term of the agreement equal to the premium cost forinterest payments that would have been made absent the long and short-term disability coverage that was in effect under plansconversion of the Company immediately before his termination or resignation;
payout note, (v)a monthly cash payment for obtain the remainderagreement of the l termDr. Rafaeli to provide certain support services to the Company, and (vi) obtain the conditional resignation of Dr. Rafaeli from our Board of Directors. Accordingly, all of our obligations under the payout notes were satisfied upon entering into the Stock Grant Agreement and the simultaneous conversion of the agreement equal to the premium cost to maintain the individual's life insurance coverage at the level of coverage in effect at the time of such termination or resignation;payout notes.
(vi)any other amounts earned, accrued and owing but not yet paid for his base salary and/or bonuses and any benefits accrued


Mr. McGrath resigned as our Chief Financial Officer on May 17, 2017. Under Mr. McGrath’s employment agreement, he was entitled to an annual base salary of $395,000, an annual bonus in an amount not less than $316,000, as well other equity compensation as determined by our Compensation Committee. In connection with Mr. McGrath’s resignation, we and Mr. McGrath agreed to convert all compensation due under any applicable benefit plans and programs of the Company; and(vii)full acceleration of all outstanding equity awards held by the individual at the time of such termination. Each outstanding option will remain exercisable until the earlier of the 60-month, or 12-month, anniversary of his termination date for Dr. Rafaeli and Mr. McGrath, respectively, and the option's expiration date.

If the Named Executive Officer does not timely execute and deliver a release, then in lieu of the foregoing payments and benefits he will only be entitled to any payments and benefits then available under the Company's then current severance pay plan or arrangement for employees without delivery of a release.
In addition, pursuant to the terms of his employment agreement upon termination Dr. Rafaeli's employment for any reason,into a secured convertible payout note to be issued following stockholder approval. On October 12, 2017, we will pay for his household relocation costs betweenissued the USpayout note in the principal amount of $977,666 to Mr. McGrath. The payout note was due on October 12, 2018, carried a ten percent (10%) interest rate, payable monthly in arrears commencing on December 1, 2017, and Israelwas secured by a security interest in all of our assets. On December 22, 2017, we entered into a Stock Grant Agreement with Mr. McGrath and reimburse him forcertain other note holders to (i) cause the early conversion of the payout note into 977,960 shares of our common stock, (ii) effectuate the release of all reasonable out of pocket relocation expenses. Additionally, we will paysecurity interests associated with the payout note, (iii) provide for the equivalentissuance of economy class airfare tickets322,727 additional shares of all family members betweencommon stock as consideration for the US and Israel.
If anyvarious agreements of the events set forthMr. McGrath contained in the table below had occurred by December 31, 2014, then we estimateStock Grant Agreement, (iv) provide for twelve (12) monthly payments of $6,653.56 on the valuefirst of each month commencing on January 1, 2018, which amounts are equal to the benefitsinterest payments that would have been triggered and thus accrued to Dr. Rafaeli andmade absent the conversion of the payout note, (v) obtain the agreement of the Mr. McGrath and had the triggering event occurred on December 31, 2014 and they timely delivered a release, would be as set forth below.

105


POTENTIAL PAYMENTS UPON TERMINATION OR CHANGE IN CONTROL TABLE
Name
 
 
Benefit
 
 
Before Change in Control Termination w/o Cause or for Good Reason ($)
 
 
After Change in Control Termination w/o Cause or for Good Reason ($)
 
 
Voluntary
Termination
 
 
Death (1)
 
 
Disability (1)
 
 
Change in Control
 
 
        
Dolev Rafaeli
Salary & bonus  (1)(2)
$ 6,780,000$6,780,000000N/A
 Health continuation22,62822,628000N/A
 AD&D insurance7,0527,052000N/A
 Executive life ins.26,60826,608000N/A
 
Accelerated vesting (3)
344,250344,250000N/A
 
TOTAL(4)
$ 7,180,538$ 7,180,538000N/A
        
Dennis McGrath
Salary & bonus  (1)(2)
$ 2,844,000$ 2,844,000000N/A
 Health continuation22,62822,628000N/A
 AD&D insurance7,0527,052000N/A
 Executive life ins.32,35232,352000N/A
 
Accelerated vesting (3)
252,450252,450000N/A
 
TOTAL(4)
$ 3,158,482$ 3,158,482000N/A


 (1)An executive's salary and benefits are paid through the end of the month of termination due to death or disability, except that we will pay the disability premiums during the period of disability.
 (2)Severance based on 2014 salary and pro-rata bonus levels. In addition to the salary and pro-rata bonus listed above, Dr. Rafaeli would be entitled to a bonus of 1% of sales for the remainder of the initial term or any renewal term.
 (3)
If upon a change of control, the acquirer does not desire theto provide certain support services of the executive, then any unvested restricted stock will vest. The closing price of our stock on December 31, 2014 was $1.53 per share.
The gain associated with the acceleration of a share of restricted stock upon a change of control is calculated as the difference between the closing price of our common stock on the date of such event and the purchase price of such share of restricted stock.
(4)The above payments are based upon the executives' employment agreements in effect as of December 31, 2014. For prospective changes to these payments and agreements, see Item 9B.
Grants of Plan-Based Awards Table
The following table sets forth certain information with respect to the options grantedCompany, and restricted stock awarded during or for(vi) obtain the year ended December 31, 2014 toconditional resignation of Mr. McGrath from our Named Executive Officers. The stock awards and option grants reflected below were awardedBoard of Directors. Accordingly, all of our obligations under the 2005 Equity Plan.
GRANTS OF PLAN-BASED AWARDS TABLE
  Estimated Possible Payouts Under Non-Equity Incentive Plan AwardsAll Other Stock Awards: Number of Shares of Stock (#)Closing Price on Grant Date ($/Sh)Grant Date Fair Value of Stock and Option Awards ($) (1)
NameGrant DateThreshold ($)Target ($)Maximum ($)   
        
Dolev Rafaeli11/7/14-$2,106,970-225,0003.12702,000
        
Dennis McGrath11/7/14-$316,000-165,0003.12514,800
        

(1)
Computed in accordance with FASB ASC Topic 718, formerly SFAS 123 (R).
106


payout notes were satisfied upon entering into the Stock Grant Agreement and the simultaneous conversion of the payout notes.

Outstanding Equity Awards Value at Fiscal Year-EndYear End Table

The following table includes certain information with respect to the value of all unexercised options and unvested shares of restricted stock previously awarded to the executive officers named above at the fiscal year end,ended December 31, 2014.

OUTSTANDING EQUITY AWARDS AT FISCAL YEAR-END TABLE
2017.

  Option Awards(1) Stock Awards(2)
Name Number of Securities Underlying Unexercised Options (#) Exercisable Number of Securities Underlying Unexercised Options (#) Un-exercisable Equity Incentive Plan Awards: Number of Securities Underlying Unexercised Unearned Options (#) Option Exercise Price ($) Option Expiration Date Number of shares or units of stock that have not vested
(#)
 Market value of shares of units of stock that have not vested
($)
 Equity incentive plan awards: Number of unearned
shares, units or other rights that have not vested
(#)
 Equity incentive
plan awards: Market or payout value of unearned
shares, units or other rights that have not vested
($)
Suneet Singal 0 0 0 N/A N/A 666,667 576,667 0 N/A
Stephen
Johnson
 0 0 0 N/A N/A 0 N/A 0 N/A
Dr. Dolev Rafaeli 28,000 0 0 100.00 3/18/2022 0 N/A 0 N/A
 9,500 0 0 100.00 2/28/2023 0 N/A 0 N/A
Dennis 1,750 0 0 31.20 6/15/19 0 N/A 0 N/A
McGrath 2,120 0 0 100.00 12/13/21 0 N/A 0 N/A
 10,020 0 0 78.00 12/13/21 0 N/A 0 N/A
 18,000 0 0 100.00 3/18/22 0 N/A 0 N/A
 7,0000 0 0 100.00 2/28/23 0 N/A 0 N/A

Option Awards
Stock Awards
Name
Number of Securities Underlying Unexercised Options (#)
Exercisable (2)
Number of
Securities Underlying Unexercised Options (#)
Unexercisable (2)
Equity Incentive Plan Awards: Number of Securities Underlying Unexercised Unearned Options (#)
Option Exercise Price ($)
Option Expiration
Date
Number of
Shares or Units
of Stock That Have Not
Vested (#)
Market Value of Shares or Units of Stock That Have Not Vested ($)(1)
Equity Incentive Plan Awards: Number of Unearned Shares, Units or Other Rights That Have Not Vested (#)
Equity Incentive
Plan Awards:
Market or Payout Value of Unearned Shares, Units or Other Rights That Have Not Vested ($) (1)
Dolev Rafaeli56,000084,000020.003/18/202200N/AN/A
 9,50038,000020.002/28/202300N/AN/A
 0N/A0N/AN/A00225,000344,250
          
Dennis McGrath8,750006.246/15/1900N/AN/A
 10,6000020.0012/13/2100N/AN/A
 50,1000015.6012/13/2100N/AN/A
 36,00054,000020.003/18/2200N/AN/A
 7,00028,000020.002/28/2300N/AN/A
 0N/A0N/AN/A00165,000252,450

(1)The market value of unvested shares of restricted stock is based on $1.53 per share, which was the closing price of our stock on December 31, 2014.
(2)All options grants were under the Amended and Restated 2005 Equity Compensation Plan.
Mr. Rafaeli and Mr. McGrath vests in the 225,000 and 165,000 shares of restricted stock, respectively, granted on November 7, 2014 equally on each of the first four anniversaries of the issuance date. The outstanding stock options vest ratably on each of the five anniversaries of the grant date.
Option Exercises and Stock Vested Table
  Option Awards Stock Awards
  Number of Shares Acquired on Exercise (#) Value Realized on Exercise ($) Number of Shares Acquired on Vesting (#) Value Realized on Vesting ($) (1)
         
Dennis M. McGrath - - 100,000 137,000
         

(2)The amount shown represents the grant of restricted stock. This amount is equal to the aggregate grant-date fair value with respect to the award made, computed in accordance with FASB ASC Topic 718 (formerly SFAS 123R).


(1)Value realized is determined by multiplying the market price of the common stock on the applicable vesting date by the number of shares that vested on that date.

107


Compensation Committee Interlocks and Insider Participation
No interlocking relationship exists between any member of our Board or Compensation Committee and any member of the board of directors or compensation committee of any other companies, nor has such interlocking relationship existed in the past.
Compensation Committee Report on Executive Compensation
The Compensation Committee has reviewed and discussed with management certain Compensation Discussion and Analysis provisions to be included herein. Based on the review and discussion referred to above, the Compensation Committee recommended to our Board of Directors that the Compensation Discussion and Analysis referred to above be included herein.
Compensation Committee
Yoav Ben-DrorStephen ConnellyLewis Pell

Director Compensation

Directors who are also our employeesexecutive officers receive no separate compensation for serving as directors or as members of committees of our Board of Directors. Directors who are not our employees are compensated under the Non-Employee Director Plan. Effective December 12, 2011, each outsideEach other director receives an annual cash retainer of $40,000, payable quarterly and the chairman of each committee receives an additional annual fee of $10,000 for audit, $5,000 for each of compensation and nominations. The table below sets forth our non-employee directors'non-executive officer directors’ compensation through December 31, 2014.  


DIRECTOR COMPENSATION TABLE
 
Name
 Fees Earned ($) Stock Awards ($) (1) 
All Other Compensation
($) (2)
 
 
Total ($)
         
Lewis Pell 40,000 0 0 40,000
         
Yoav Ben-Dror 45,000 0 360,000 405,000
         
Katsumi Oneda 30,000 0 0 30,000
         
James W. Sight 45,000 0 0 45,000
         
Stephen P. Connelly 40,000 0 0 40,000
         
Trevor S. Harris 37,500 74,700 0 112,200
2017.  

 

 

Name 

 Fees earned
or paid in
cash ($)
  

All other compensation 

($) 

  

 

 

Total ($) 

 
Dr. Robert Froehlich(1)  28,125   0   28,125 
Richard J. Leider(1)  28,125   0   28,125 
Darrell C. Menthe(1)  25,000   0   25,000 
Michael R. Stewart(1)  31,250   0   31,250 

Lewis Pell(2)

  

17,100

   0   

  17,100

 
Dr. Yoav Ben-Dror(2)(3)  

15,200

   

960,134

   

975,334

 

Stephen P. Connelly(2)

  

17,100

   0   

             17,100

 

Dennis McGrath(4)

  25,000   

1,003,983

   

           1,028,983

 

Dr. Dolev Rafaeli(4)

  25,000   

3,347,065

   

             3,372,065

 

(1)
New Directors compensated for the period of May 17, 2017 through December 31, 2017.

(2)Lewis C. Pell, Dr, Ben-Dror, and Stephen P. Connelly, resigned from the Board effective May 17, 2017.

(3)We and Dr. Ben-Dror agreed to convert all compensation due under his previous agreements into a secured convertible payout note to be issued following stockholder approval. On October 12, 2017, we issued the payout note in the principal amount of $1,515,000 to Dr. Ben-Dror. The amounts shownpayout note was due on October 12, 2018, carried a ten percent (10%) interest rate, payable monthly in arrears commencing on December 1, 2017, and was secured by a security interest in all of our assets. On December 22, 2017, we entered into a Stock Grant Agreement with Dr. Ben-Dror and certain other note holders to (i) cause the early conversion of the payout note into 1,515,455 shares of our common stock, (ii) effectuate the release of all security interests associated with the payout note, (iii) provide for the issuance of 500,100 additional shares of common stock awards relate to shares granted under our Non-Employee Director Plan. Theseas consideration for the various agreements of Dr. Ben-Dror contained in the Stock Grant Agreement, (iv) provide for twelve (12) monthly payments of $10,310.42 on the first of each month commencing on January 1, 2018, which amounts are equal to the aggregate grant-date fair value with respectinterest payments that would have been made absent the conversion of the payout note, and (v) obtain the agreement of the Dr. Ben-Dror to provide certain support services to the stock awards for financial statement purposes.
(2)Dr. Ben-Dror receives a monthly payment of $30,000 for his services as the executive director for Radiancy Ltd. and Photo Therapeutics, Ltd.Company.

108


Limitation on Directors' Liabilities; Indemnification of Officers and Directors
Our Articles of Incorporation and bylaws designate the relative duties and responsibilities of our officers, establish procedures for actions by directors and stockholders and other items. Our Articles of Incorporation and bylaws also contain extensive indemnification provisions, which will permit us to indemnify our officers and directors to the maximum extent provided by Nevada law. Pursuant to our Articles of Incorporation and under Nevada law, our directors are not liable to us or our stockholders for monetary damages for breach of fiduciary duty, except for breaches which involve intentional misconduct, fraud or a knowing violation of law.
Directors' and Officers' Liability Insurance
We have obtained directors' and officers' liability insurance, which expires on December 13, 2015. We are required under our indemnification agreements to maintain such insurance for us and members of our Board of Directors. We also provided tail insurance for the directors of Radiancy.

(4)See Summary Compensation Table – Fiscal Years Ended December 31, 2017 and 2016.

Item 12.
ITEM 12.SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED STOCKHOLDER MATTERS.

Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters

The information set forth in Item 5 of this Annual Report under the heading "Overview of Equity Compensation Plans" is hereby incorporated by reference.

The following table reflects,sets forth information regarding beneficial ownership of our voting stock as of March 13, 2015, the beneficial common stock ownership of: (a)30, 2018 (i) by each of our directors, (b) each executive officer, (c) each person who is known by us to be a beneficial holder of five percent (5%) orbeneficially own more than 5% of our common stock,voting stock; (ii) by each of our officers and (d)directors; and (iii) by all of our executive officers and directors as a group. Unless otherwise providedspecified, the address of each of the persons set forth below is in care of the accompanying footnotes, the information used in the table below was obtained from the referenced beneficial owner.

Name and Address Of Beneficial Owner (1)
Number of Shares Beneficially Owned
Percentage of Shares Beneficially Owned (1)
Lewis C. Pell (2)
2,120,3199.54%
Yoav Ben-Dror (3)
1,553,4217.01%
Dolev Rafaeli (4)
1,583,3477.13%
Dennis M. McGrath (5)
429,2741.93%
James W. Sight (6)
479,4962.16%
Stephen P. Connelly (7)
20,194*
Trevor Harris (8)
5,000*
Katsumi Oneda (9)
1,325,1646.00%
Shlomo Ben-Haim (10)
1,806,2638.17%
Paradigm Capital Mgt. (11)
1,230,7005.57%
Stonepine Capital L.P.  (12)
1,206,7895.46
All directors and officers as a group (seven persons) (13)
6,191,05127.88%
Company, 40 Ramland Road South, Suite 200, Orangeburg, NY 10962.

Name and Address of Beneficial Owner Amount of Beneficial
Ownership(1)
  

Percent  

of Common Stock(2) 

  Percent of
Series B
Preferred
Stock(3)
  Percent of
Total
Voting
Stock(4)
 
 Common
Stock
  Series B
Preferred
Stock
       
Vineet P. Bedi, Chief Executive Officer  0   0    *  0    *
Matthew Stolzar, Chief Financial Officer  0   0    *  0    *
Bob Froehlich, Chairman of the Board  58,159   0   0.52  0   0.34
Richard J. Leider, Director  0   0    *  0    *
Dennis M. McGrath, Director(5)  1,068,128   0   9.45%  0   6.24%
Dr. Dolev Rafaeli, Director(6)  3,355,900   0   29.71%  0   19.60%
Michael R. Stewart, Director  0   0    *  0    *
All directors and officers as a group (7 persons named above)  4,482,187   0   39.54%  0   26.12%

Dr. Yoav Ben-Dror 

66 Pinkas st 

Tel Aviv 6215719 Israel 

  1,814,639   0   16.12%  0   10.62%

Suneet Singal(7) 

410 Park Ave, 14th Floor 

New York, NY 10022 

  1,212,567   0   10.77%  0   7.10%

Opportunity Fund I-SS, LLC(8) 

c/o OP Fund I Manager, LLC
2481 Sunrise Blvd, Suite 200
Gold River, CA 95670 

  0   3,725,000    *  100%  34.10%


*Less than 1%.

(1)Beneficial ownershipOwnership is determined in accordance with the rules of the Commission. SharesSEC and generally includes voting or investment power with respect to securities. Each of common stock subject to delivery, or subject to options or warrants currently exercisable or exercisable, within 60 days of March 13, 2015, are deemed outstanding for computing the percentagebeneficial owners listed above has direct ownership of the stockholder holding the options or warrants, but are not deemed outstanding for computing the percentage ownership of any other stockholder. Unless otherwise indicated in the footnotes to this table, we believe stockholders named in the table haveand sole voting power and sole investment power with respect to the shares set forth opposite such stockholder's name. Unless otherwise indicated, the listed officers, directors and stockholders can be reached atof our principal offices. Percentagecommon stock.

(2)Based on 11,868,619 shares of ownership is based on 22,101,718 shares ofour common stock outstanding as of March 13, 2015.30, 2018. For each beneficial owner above, any options exercisable within 60 days have been included in the denominator.
109

(2)(3)Includes 1,405,319Based on 3,725,000 shares of our Series B Preferred Stock outstanding as of March 30, 2018. Shares of Series B Preferred Stock are convertible into shares of common stock 600,000 shares held by trusts with respect to which Mr. Pell may be deemed to have beneficial ownership and warrants to purchase 115,000 shareson the basis of common stock. Mr. Pell's address is 100 Lakeside Drive, Suite 100, Horsham, PA 19044.
(3)Includes 1,495,921approximately 1.56 shares of common stock beneficially owned,for each share of which 1,370,843 shares are owned directly by Dr. Ben-Dror and 125,078 shares are owned by Gohan Investments Ltd.Series B Preferred Stock. Holders of which Dr. Ben-Dror isSeries B Preferred Stock vote with the 100% owner, and warrants to purchase 57,500 shares of common stock. Dr. Ben-Dror's address is 100 Lakeside Drive, Suite 100, Horsham, PA 19044.
(4)Includes 1,255,347 sharesholders of common stock 225,000 additionalon all matters on an as-converted to common stock basis.

(4)Percentage of Total Voting Stock represents total ownership with respect to all shares of our common stock subjectand Series B Preferred Stock, as a single class and on an as-converted to restriction agreements with us and vested options to purchase 103,000 shares of common stock. Does not include unvested options to purchase up to 84,500 shares of common stock which may vest more thanbasis. For each beneficial owner above, any options exercisable within 60 days after March 13, 2015.have been included in the denominator.

(5)
Includes 91,136 shares of common stock, 165,000 additional shares of common stock subject to restriction agreements with us, warrants to purchase 35,6881,029,238 shares of common stock and vested options to purchase 137,45038,890 shares of common stock. Does not include options to purchase up to 57,000 shares of common stock, which may vest more than 60 days after March 13, 2015.

(6)
Includes 346,208 shares of common stock and warrants to purchase 133,288 shares of common stock. Mr. Sight's address is 100 Lakeside Drive, Suite 100, Horsham, PA 19044.
(7)Includes 15,689 shares of common stock, 250 shares held by trusts with respect to which Mr. Connelly may be deemed to have beneficial ownership, warrants to purchase 3,422 shares of common stock and options to purchase up to 833 shares of common stock. Mr. Connelly's address is 100 Lakeside Drive, Suite 100, Horsham, PA 19044.
(8)
Includes 5,000 shares of common stock. Mr. Harris's address is 100 Lakeside Drive, Suite 100, Horsham, PA 19044.
(9)Includes 1,005,164 shares of common stock and 320,000 shares held by trusts with respect to which Mr. Oneda may be deemed to have beneficial ownership. Mr. Oneda's address is 100 Lakeside Drive, Suite 100, Horsham, PA 19044.
(10)Shlomo Ben-Haim is, or may be deemed to be, the beneficial owner of 1,806,263 shares of common stock. Of the 1,806,263 shares, 1,153,858 shares are owned by Eastnet Investment Limited and 402,250 shares are owned by Antinori, Ltd. Mr. Ben-Haim has voting and/or dispositive power over shares held by Eastnet Investment Limited and Antinori, Ltd. Mr. Ben-Haim's address is 8 Kensington Palace Gardens, London W84QP, United Kingdom. Eastnet Investment Limited's address is Nerine Chambers, PO Box 905, Road Town, Tortola, British Virgin Islands. Antinori Ltd.'s address is Alon Tavor 15, Industrial Zone, Caesarea, Israel.
(11)Paradigm Capital Management is, or may be deemed to be, the beneficial owner of 1,230,700 shares of common stock. The foregoing information has been derived in part from a Schedule 13G filed on February 11, 2015. Paradigm Capital Management's address is Nine Elk Street, Albany, NY 12207.
(12)Stonepine Capital L.P. Stonepine Capital Management, LLC, Jon M. Plexico and Timothy P. Lynch are, or may be deemed to be, the beneficial owners of 1,206,789 shares of common stock. The foregoing information has been derived in part from a Schedule 13G filed on March 9, 2015. The principal business address of the filers is 475 Gate Five Road, Suite 324, Sausalito, CA  94965.
(13)Includes 4,614,620 unrestricted shares of common stock, including 600,250 held by trusts, and 390,000 restricted shares of common stock warrants to purchase 344,8983,318,400 shares of common stock and vested options to purchase 241,28337,500 shares of common stock. Does not include options to purchase up to 141,500

(7)Includes 879,234 shares of common stock held by First Capital Real Estate Operating Partnership, LP. Mr. Singal is the Chief Executive Officer of First Capital Real Estate Trust Incorporated, which mayis the general partner of First Capital Real Estate Operating Partnership, LP. Mr. Singal disclaims beneficial ownership of such shares. Also includes 333,333 shares of common stock held directly by Mr. Singal. Does not include 666,667 shares of common stock that do not vest more thanwithin 60 days after March 13, 2015.days.
110

(8)Kristen Pigman is the Director of OP Fund I Manager, LLC, which is the member and manager ofOpportunity Fund I-SS, LLC, and has voting and dispositive power over the securities held by it. Mr. Pigman disclaims beneficial ownership of such securities.

Changes in Control

On December 22, 2017, we entered into a Securities Purchase Agreement with OFI under which OFI may invest up to $15 million in the Company in a series of closings, in exchange for which OFI will receive shares of our Series B Preferred Stock, at a purchase price of $1.00 per share. A change of control of the Company may occur if OFI invests such maximum amount. We do not currently have any other arrangements which if consummated may result in a change of control of the Company

Securities Authorized for Issuance under Equity Compensation Plans

The following is a summary of all of our equity compensation plans, including plans that were assumed through acquisitions and individual arrangements that provide for the issuance of equity securities as compensation, as of December 31, 2017. See Notes 1 and 12 to the consolidated financial statements for additional discussion.


(In thousands, except share and per share amounts)

EQUITY COMPENSATION PLAN INFORMATION

  

Number of Securities to be Issued Upon Exercise of Outstanding Options, Warrants and Rights

  

Weighted-Average Exercise Price of Outstanding Options, Warrants and Rights

  

 Number of Securities Remaining Available for Future Issuance Under Equity Compensation Plans (excluding securities reflected in column (A)) 

 
  (A)  (B)  (C) 
Equity compensation plans approved by security holders  1,000  $75.00   147,088 
Equity compensation plans not approved by security holders         
Total  1,000  $75,00   147,088 

Options have been granted to employees and/or consultants out of our 2005 Equity Compensation Plan. Restricted stock awards of 6,500 thousand were issued but not vested as of December 31, 2017. Options to our outside directors will be made from our 2000 Non-Employee Director Stock Option Plan. Additionally, all outstanding options were granted as compensation for benefits inuring to us other than for benefits from capital-raising activities. With limited exceptions under Nasdaq membership requirements, we intend in the future to issue options pursuant to equity compensation plans which have already been approved by our stockholders.

ITEM 13.CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCE.

Item 13.    Transactions with Related PersonsCertain Relationships

The following includes a summary of transactions since the beginning of our 2016 fiscal year, or any currently proposed transaction, in which we were or are to be a participant and Related Transactions, the amount involved exceeded or exceeds the lesser of $120 or one percent of the average of our total assets at year-end for the last two completed fiscal years, and in which any related person had or will have a direct or indirect material interest (other than compensation described under “Executive Compensation”). We believe the terms obtained or consideration that we paid or received, as applicable, in connection with the transactions described below were comparable to terms available or the amounts that would be paid or received, as applicable, in arm’s-length transactions. (All amounts in thousands, except share and per share amounts.)

On August 3, 2017, October 11, 2017 and December 22, 2017, we entered into amendments to the Contribution Agreement. Suneet Singal, our Chief Executive Officer and Director at the time that we entered into such amendments, is also the Chief Executive Officer of the Contributor Parent, which is the general partner of the Contributor.

On December 22, 2017, we entered into a Letter Agreement with Suneet Singal and certain entities related to or affiliated with him, including the Contributor Parties, pursuant to which Mr. Singal and such entities agreed that they would not, without the prior written consent of OFI, transfer or otherwise dispose of any or all of our equity securities held them, including any additional equity securities which they may subsequently acquire, until 180 days following the dissolution of OFI, but no later than December 31, 2018, subject to certain exceptions.

On October 22, 2017, all amounts due to Dr. Dolev Rafaeli and Dennis M. McGrath under their employment agreements, as well as amounts due to Dr. Yoav Ben-Dror for his services as a board member and officer of our foreign subsidiaries, were converted to secured convertible payout notes in the principal amounts of $3,134, $978 and $1,515, respectively. These payout notes were due on October 12, 2018, carried a ten percent (10%) interest rate, payable monthly in arrears commencing on December 1, 2017, and were secured by a security interest in all of our assets.


On December 22, 2017, we entered into the Stock Grant Agreement with Dr. Dolev Rafaeli, Dennis M. McGrath and Dr. Yoav Ben-Dror to (i) cause the early conversion of the payout notes into an aggregate of 5,628,291 shares of our common stock, (ii) effectuate the release of all security interests associated with the payout notes, (iii) provide for the issuance of an aggregate of 1,857,336 additional shares of common stock as consideration for the various agreements of such note holders contained in the Stock Grant Agreement, (iv) provide for twelve (12) monthly payments of approximately $21, $7 and $10 to Messrs. Rafaeli, McGrath, and Ben-Dror, respectively, on the first of each month commencing on January 1, 2018, which amounts are equal to the interest payments that would have been made absent the conversion of the payout notes, (v) obtain the agreement of such note holders to provide certain support services to us, and (vi) obtain the conditional resignation of Messrs. Rafaeli and McGrath from our Board of Directors. Accordingly, the payout notes were paid in full.

On December 22, 2017, we entered into a Registration Rights Agreement with Dr. Dolev Rafaeli, Dennis M. McGrath and Dr. Yoav Ben-Dror, pursuant to which we agreed to register the 1,857,336 additional shares to be issued under the Stock Grant Agreement under the Securities Act.

OFI has made certain loans to the Contributor or one of its affiliates under a separate transaction, which are secured by the Series A Preferred Stock and the Common Stock issued to the Contributor pursuant to the Contribution Agreement on May 17, 2017. At the time of the OFI transaction with our company, Suneet Singal was Chief Executive Officer and a member of our Board of Directors and was also the Chief Executive Officer of the Contributor Parent. Accordingly, the Purchase Agreement between the Company and OFI was considered an interested party transaction and was approved by a majority of our non-interested directors.

Director Independence

Related Person Transactions
We have entered into an indemnification agreement with each

Our Board of our directors pursuant to which we have agreed to indemnify each director against claims brought against them in their capacities as our directors. These indemnification agreements also require us to maintain directors' and officers' liability insurance for our directors.

On December 12, 2014, the Company entered into a Securities Purchase Agreement with certain investors including three directors, James Sight, Yoav Ben-Dror, and Lewis C. Pell. Mr. Sight purchased 150,000 shares of the Company's common stock at a price of $2.19 per share and warrants to purchase 75,000 shares with an exercise price of $2.25 per share. Mr. Ben-Dror purchased 115,000 shares of common stock at a price of $2.19 per share and warrants to purchase 57,500 shares with an exercise price of $2.25 per share. Mr. Pell purchased 230,000 shares of common stock at a price of $2.19 per share and 115,000 warrants to purchase 115,000 shares with an exercise price of $2.25 per share. The warrants purchased by all three directors are exercisable beginning on December 12, 2015 until December 12, 2017.
We believe that all transactions with our affiliates have been entered into on terms no less favorable to us than could have been obtained from independent third parties. We intend that any transactions with officers, directors and 5% or greater stockholders will be on terms no less favorable to us than could be obtained from independent third parties and will be approved by a majority of our independent, disinterested directors and will comply with the Sarbanes-Oxley Act of 2002, as amended, and other securities laws and regulations.
Director Independence
As required under the NASDAQ Stock Market LLC, or NASDAQ, listing standards, a majority of the members of a listed company's board of directors must qualify as "independent," as affirmativelyDirectors has determined by the board of directors. Our board of directors consults with internal counsel to ensure that the board's determinations are consistent with relevant securities and other laws and regulations regarding the definition of "independent," including those set forth in pertinent NASDAQ listing standards, as in effect from time to time. Consistent with these considerations, after review of all relevant transactions or relationships between each director, or any of his or her family members, and our company, our senior management and our independent registered public accounting firm, the board of directors has affirmatively determined that all of our currentfollowing directors are independent directors withinas defined in the meaningapplicable rules of the applicable NASDAQ listing standards, except for Messrs. RafaeliNasdaq Stock Market: Dr. Bob Froehlich, Richard J. Leider and McGrath, who are our Chief Executive Officer and Chief Financial Officer, respectively, who are not independent directors by virtue of their employment with our company.
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Michael R. Stewart. 

Item 14.    Principal Accounting Fees and Services
ITEM 14.PRINCIPAL ACCOUNTING FEES AND SERVICES.

We engaged Fahn Kanne & Co. Grant Thornton Israel ("Grant Thornton Israel") as our independent auditors for 20142017 and 2013.

2016. The following table shows the fees paid or accrued by us for the audit and other services provided by Fahn Kanne & Co. Grant Thornton Israel for 20142017 and 2013:
  2014 2013
Audit Fees (1)
 $474,500 $327,000
Audit-Related Fees (2)
 18,000 18,000
Tax Fees (3)
 368,000 126,000
All Other Fees (4)
 - 116,000
Total $860,500 $587,000
2016:

(In thousands)

  2017  2016 
Audit Fees(1) $200  $200 
Audit-Related Fees(2)      
Tax Fees(3)  105   433 
Total $305  $633 

(1)Consists of fees billed for the audit of our annual financial statements, review of financial statements included in our Quarterly Reports on Form 10-Q and services that are normally provided by the auditors in connection with statutory and regulatory filings or engagements.

(2)Consists of assurance and related services that are reasonably related to the performance of the audit and reviews of our financial statements and are not included in "audit fees"“audit fees” in this table, principally related to the limited scope audit of the 401(K) plan and due diligence services.

(3)Consists of all tax related services.


(4)
Consists of all other products and services provided other than the services reported under audit fees, audit related fees and tax fees.

EngagementPre-Approval Policies and Procedures

Under the Sarbanes-Oxley Act of the Independent Auditor. The Audit Committee is responsible for approving every engagement of Grant Thornton Israel to perform audit or non-audit services for us before Grant Thornton Israel is engaged to provide those services. Under applicable Commission rules, the Audit Committee is required to pre-approve the2002, all audit and non-audit services performed by the independentour auditors must be approved in orderadvance by our board of directors to ensureassure that theysuch services do not impair the auditors' independence. The Commission's rules specifyauditors’ independence from us. In accordance with its policies and procedures, our board of directors pre-approved the types of non-audit services that an independent auditor may not provide to its audit client and establish the Audit Committee's responsibility for administration of the engagement of the independent auditors.

Consistent with the Commission's rules, the Audit Committee Charter requires that the Audit Committee review and pre-approve all audit services and permitted non-audit services providedservice performed by the independent auditors to us or any of our subsidiaries. The Audit Committee may delegate pre-approval authority to a member of the Audit Committee and if it does, the decisions of that member must be presented to the full Audit Committee at its next scheduled meeting.
The Audit Committee's pre-approval policy provides as follows:
·  First, once a year when the base audit engagement is reviewed and approved, management will identify all other services (including fee ranges) for which management knows it will engageFahn Kanne & Co. Grant Thornton Israel for the next 12 months. Those services typically include quarterly reviews, specified tax matters, certifications to the lendersour financial statements as required by financing documents, consultation on new accountingof and disclosure standards and, in future years, reporting on management's internal controls assessment.
·  Second, if any new "unlisted" proposed engagement arises during the year, the engagement will require approval of the Audit Committee.
All fees to our independent accounting firms were approved by the Audit Committee.
Auditor Selection for Fiscal 2015 The Audit Committee has selected Grant Thornton Israel to serve as our independent auditors for the year ending December 31, 2015. The Committee's selection will be submitted to our stockholders for ratification at our 2015 Annual Meeting of Stockholders.
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PART IV
Item 15.    Exhibits and Financial Statement Schedules 
    (a)(1)  Financial Statements
Consolidated balance sheets of PhotoMedex, Inc. and subsidiaries as of December 31, 2014 and 2013, and the related consolidated statements of comprehensive (loss) income, changes in' equity and cash flows for each of the years in the three-year period ended December 31, 2014.
2017.

(a)PART IV

ITEM 15.EXHIBITS, FINANCIAL STATEMENT SCHEDULES.

a)List of Documents Filed as a Part of This Report:

(1)Index to Financial Statements:

Report of Independent Registered Public Accounting Firm F-2
Consolidated Balance Sheets, December 31, 2017 and 2016 F-3
Consolidated Statements of Comprehensive Loss, Years ended December 31, 2017 and 2016 F-4

Consolidated Statements of Changes in Redeemable Convertible Preferred Stock and Stockholders’ Deficit, Years ended December 31, 2017 and 2016

F-5
Consolidated Statements of Cash Flows, Years ended December 31, 2017 and 2016 F-6
Notes to Consolidated Financial StatementsF-8-F-47

(2)Index to Financial Statement SchedulesSchedules:

All schedules have been omitted because they are notthe required not applicable, or the information is otherwise set forthincluded in the consolidated financial statements or the notes thereto.

thereto, or because it is not required.

(a)(3)Index to Exhibits:Exhibits

The

See exhibits listed under subsectionsPart (b) of this Item 15 are hereby incorporated by reference.


below.

(b)Exhibits:Exhibits

2.1Exhibit No.
Amended and Restated Description
2.1Agreement and Plan of Merger and Reorganization, dated as of October 31, 2011,February 19, 2016, by and among DS Healthcare Group, Inc., PHMD Consumer Acquisition Corp., the Company, and Radiancy, Inc., PhotoMedex, Inc. and PHMD Merger Sub, Inc., including (incorporated by reference to Exhibit 2.1 to the Current Report on Form of Warrant. (238-K filed on February 22, 2016))
2.2
2.2Agreement and Plan of Merger by and among PhotoMedex, Inc., Gatorade Acquisition Corp. and LCA-Vision Inc.,Reorganization, dated as of February 13, 2014 (34)19, 2016, by and among DS Healthcare Group, Inc., PHMD Professional Acquisition Corp., the Company, and PhotoMedex Technology, Inc. (incorporated by reference to Exhibit 2.2 to the Current Report on Form 8-K filed on February 22, 2016)
3.1
3.1Amended and Restated Articles of Incorporation of PhotoMedex, Inc. athe Company filed with Nevada corporation,Secretary of State on October 19, 2017 (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K filed on October 25, 2017)
3.2Certificate of Designation of Series A Convertible Preferred Stock filed with Nevada Secretary of State on May 17, 2017 (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K filed on May 19, 2017)
3.3Certificate of Designation of Series B Preferred Stock filed with Nevada Secretary of State on December 22, 2017 (incorporated by reference to Exhibit 3.1 to the Current Report on Form 8-K filed on December 12, 2011 with the Secretary of State for the State of Nevada. (23)29, 2017)
3.2
3.4Amended and Restated Bylaws of PhotoMedex, Inc. (a Nevada corporation),the Company adopted December 28, 2010 (18)on May 17, 2017 (incorporated by reference to Exhibit 10.6 to the Current Report on Form 8-K filed on May 19, 2017)


4.110.1Securities Purchase Agreement, dated December 22, 2017, between the Company and Opportunity Fund I-SS, LLC (incorporated by reference to Exhibit 10.1 to the Current Report on Form of Warrant to Purchase Shares of Common Stock of PhotoMedex (19)8-K filed on December 29, 2017)
4.2Term Loan
10.2Registration Rights Agreement, dated December 22, 2017, between the Company and SecurityOpportunity Fund I-SS, LLC (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed on December 29, 2017)
10.3Letter Agreement, dated December 22, 2017, among the Company, Opportunity Fund I-SS, LLC, Suneet Singal, First Capital Real Estate Trust Incorporated, First Capital Real Estate Operating Partnership, L.P. and First Capital Real Estate Investments LLC (incorporated by reference to Exhibit 10.3 to the Current Report on Form 8-K filed on December 29, 2017)
10.4Interest Contribution Agreement, dated March 31, 2017, by and among First Capital Real Estate Operating Partnership, L.P., First Capital Real Estate Trust Incorporated, FC Global Realty Operating Partnership, LLC and the Company (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on April 3, 2017)
10.5Agreement to Waive Closing Deliverables, dated as of May 17, 2017, by and among the Company, FC Global Realty Operating Partnership, LLC, First Capital Real Estate Operating Partnership, L.P. and First Capital Real Estate Trust Incorporated (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on May 19, 2017)
10.6Registration Rights Agreement, dated as of MarchMay 17, 2017, among the Company and certain holders (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed on May 19, 2010 between PhotoMedex, Inc. and Clutterbuck Funds LLC (26) (Exhibit 4.12 therein)2017)
4.3Term
10.7Assignment and Assumption Agreement, dated as of May 17, 2017, by and between First Capital Real Estate Operating Partnership, L.P., First Capital Real Estate Trust Incorporated, FC Global Realty Operating Partnership, LLC, and the Company (incorporated by reference to Exhibit 10.3 to the Current Report on Form 8-K filed on May 19, 2017)
10.8Lock-Up and Resale Restriction Agreement, dated as of May 17, 2017, among the Company and certain holders (incorporated by reference to Exhibit 10.4 to the Current Report on Form 8-K filed on May 19, 2017)
10.9Assignment and Assumption Agreement, dated June 26, 2017, by and between First Capital Real Estate Operating Partnership, L.P., First Capital Real Estate Trust Incorporated, FC Global Realty Operating Partnership, LLC, and the Company (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on June 28, 2017)
10.10Agreement to Waive Closing Deliverables, dated as of July 3, 2017, by and among the Company, FC Global Realty Operating Partnership, LLC, First Capital Real Estate Operating Partnership, L.P. and First Capital Real Estate Trust Incorporated (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on July 10, 2017)
10.1120% Unsecured Promissory Note, dated March 19, 2010,July 25, 2017, by and between PhotoMedex, Inc.the Company and Clutterbuck Funds, LLC (26) (Exhibit 4.13 therein)First Capital Real Estate Operating Partnership L.P. (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on July 31, 2017)
4.4
10.12Amendment No. 1 to Term Loan and SecurityInterest Contribution Agreement, dated April 30, 2010 (27) (Exhibit 4.20 therein)August 3, 2017, among First Capital Real Estate Operating Partnership, L.P., First Capital Real Estate Trust Incorporated, FC Global Realty Operating Partnership, LLC and the Company (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed on August 3, 2017)
4.5
10.13Second Agreement to Waive Closing Deliverables, dated September 22, 2017, by and among the Company, FC Global Realty Operating Partnership, LLC, First Capital Real Estate Operating Partnership, L.P. and First Capital Real Estate Trust Incorporated (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on September 28, 2017)
10.14Amendment No. 2 to Term Loan and SecurityInterest Contribution Agreement, dated March 28, 2011 (27) (Exhibit 4.21 therein)October 11, 2017, among First Capital Real Estate Operating Partnership, L.P., First Capital Real Estate Trust Incorporated, FC Global Realty Operating Partnership, LLC and the Company (incorporated by reference to Exhibit 10.3 to the Current Report on Form 8-K filed on October 18, 2017)


4.610.15CreditAmendment No. 3 to Interest Contribution Agreement, dated December 27, 2013, between22, 2017, among First Capital Real Estate Operating Partnership, L.P., First Capital Real Estate Trust Incorporated, FC Global Realty Operating Partnership, LLC and the Company (incorporated by reference to Exhibit 10.7 to the Current Report on Form 8-K filed on December 29, 2017)
10.16Asset Purchase Agreement, dated October 4, 2016, by and among ICTV Brands Inc., ICTV Holdings, Inc., the Company, Radiancy, Inc., PhotoTherapeutics Ltd. and JP Morgan Chase Bank, N.A. (35)Radiancy (Israel) Limited (incorporated by reference to Exhibit 2.1 to the Current Report on Form 8-K filed on October 5, 2016)
10.1Lease
10.17Escrow Agreement, dated May 29, 1996, between Surgical Laser Technologies,October 4, 2016, by and among ICTV Brands Inc., ICTV Holdings, Inc., the Company, Radiancy, Inc., PhotoTherapeutics Ltd., Radiancy (Israel) Limited, those investors listed on the Schedule of Investors attached thereto, and Nappen & Associates (Montgomeryville, Pennsylvania) (2)Bevilacqua PLLC (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on October 5, 2016)
10.2Lease Renewal
10.18Transition Services Agreement, dated October 4, 2016, by and among ICTV Holdings, Inc., the Company, Radiancy, Inc., PhotoTherapeutics Ltd. and Radiancy (Israel) Limited (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed on October 5, 2016)
10.19First Amendment to the Asset Purchase Agreement, dated January 18, 2001, between Surgical Laser Technologies,23, 2017, ICTV Brands Inc., ICTV Holdings, Inc., the Company, Radiancy, Inc., PhotoTherapeutics Ltd. and Nappen & Associates (2)Radiancy (Israel) Limited (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on January 24, 2017)
10.3Lease
10.20First Amendment to the Transition Services Agreement, dated January 23, 2017, by and among ICTV Holdings, Inc., the Company, Radiancy, Inc., PhotoTherapeutics Ltd. and Radiancy (Israel) Limited (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed on January 24, 2017)
10.21Termination and Release Agreement, dated July 10, 2006, PhotoMedex, Inc. and Nappen & Associates (3)
10.4Standard Industrial/Commercial Multi-Tenant Lease - Net, dated July 30, 2008 (additional facility at Carlsbad, California) (15)
10.5Standard Industrial/Commercial Multi-Tenant Lease  Net, dated March 17, 2005 (Carlsbad, California) (5)
10.6License and Development Agreement, dated May 22, 2002, between Surgical Laser Technologies, Inc. and Reliant Technologies, Inc. (2)
10.7Settlement Agreement and Release, dated November 11, 2008,12, 2017, by and among Allergan,ICTV Brands Inc., Murray A. Johnstone, MD, PhotoMedex,ICTV Holdings, Inc., the Company, Radiancy, Inc., PhotoTherapeutics Ltd. and ProCyte Corporation. (15)Radiancy (Israel) Limited (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on July 18, 2017)
10.8Master
10.22Bill of Sale, dated July 12, 2017, by and among the Company, Radiancy, Inc., PhotoTherapeutics Ltd., Radiancy (Israel) Limited and ICTV Holdings, Inc. (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed on July 18, 2017)
10.23Asset Purchase Agreement, dated August 30, 2016, among Pharma Cosmetics Laboratories Ltd., Pharma Cosmetics Inc., the Company and PhotoMedex Technology, Inc. (incorporated by reference to Exhibit 2.1 to the Current Report on Form 8-K filed on September 6, 2016)
10.24First Amendment to the Asset Purchase Agreement, dated September 7, 2004, between15, 2016, among Pharma Cosmetics Laboratories Ltd., Pharma Cosmetics Inc., the Company and PhotoMedex Technology, Inc. (incorporated by reference to Exhibit 2.1 to the Current Report on Form 8-K filed on September 20, 2016)
10.25First Amendment to the Transition Services Agreement, dated September 15, 2016, among the Company, PhotoMedex Technology, Inc. and Stern Laser, srl (6)Pharma Cosmetics Inc. (incorporated by reference to Exhibit 2.2 to the Current Report on Form 8-K filed on September 20, 2016)
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10.9License
10.26Asset Purchase Agreement, dated March 31, 2006, and effective April 1, 2006, between the Mount Sinai School of Medicine and PhotoMedex, Inc. (7)
10.102005 Equity Compensation Plan, approved December 28, 2005 (8)
10.11Amended and Restated 2000 Non-Employee Director Stock Option Plan (1)
10.12Amended and Restated 2000 Stock Option Plan (1)
10.131996 Stock Option Plan, assumed from ProCyte (9)
10.16Restricted Stock Purchase Agreement of Dennis M. McGrath, dated January 15, 2006 (5)
10.17Consulting Agreement dated January 21, 199811, 2015, between the Company and R. Rox Anderson, M.D. (4)The Lotus Global Group, Inc. dba GlobalMed Technologies Co. (incorporated by reference to Exhibit 10.74 to the Quarterly Report on Form 10-Q filed on May 13, 2016)
10.18Restricted Stock Purchase Agreement of Dennis M. McGrath, dated May 1, 2007 (10)
10.2110.27Amended and Restated 2000 Non-Employee Director Stock Option Plan, dated as of June 26, 2007 (24)
10.22Amended and Restated 2005 Equity Compensation Plan, dated as of June 26, 2007, as amended on October 28, 2008 (14)
10.23Form of Indemnification Agreement for directors and executive officers of PhotoMedex, Inc. (13)
10.24Restricted StockAsset Purchase Agreement of Dennis M. McGrath, dated June 15, 2009 (16)
10.26Co-Promotion Agreement, dated as of January 7, 2010, between PhotoMedex, Inc and Galderma Laboratories, L.P. (17)
10.27Amended and Restated 2000 Non-Employee Director Stock Option Plan, dated as of August 3, 2010 (18)
10.28Amended and Restated 2005 Equity Compensation Plan, dated as of August 3, 2010. (18)
10.29Restricted Stock Agreement of Dennis M. McGrath, dated March 30, 2011 (18)
10.32Amended and Restated Employment agreement, entered into by and between PhotoMedex, Inc. and Dennis McGrath on July 4, 2011. (19)
10.33Amended and Restated Restricted Stock Agreement, entered into as of August 11, 2011, by and between PhotoMedex, Inc. and Dennis McGrath. (20)
10.34Restricted Stock Agreement, entered into as of July 4, 2011, by and between PhotoMedex, Inc. and Dennis McGrath. (19)
10.35Non-Qualified Stock Option Agreement, entered into as of July 4, 2011, by and between PhotoMedex, Inc. and Dennis McGrath. (19)
10.40Amended and Restated Employment Agreement entered into by and between PhotoMedex, Inc. and Dolev Rafaeli on August 9, 2011. (21)
10.41Distribution Agreement by and between Radiancy, Inc. and Ya-Man Ltd., dated October 17, 2008. (21)
10.42Distribution Agreement Extension by and between Radiancy, Inc. and Ya-Man Ltd., dated August 12, 2010. (21)
10.43First Amendment to the Nonqualified Stock Option Agreement, dated as of October 31, 2011, by and between PhotoMedex, Inc. and Dennis McGrath (22)
10.45Lease Renewal Agreement, dated February 22, 2012, PhotoMedex, Inc. and FR National Life LLC (28)
10.46Lease Agreement, dated September 1, 2010,2015, among DaLian Jikang Medical Systems Import & Export Co., LTD, the Company and PhotoMedex Technology, Inc. (incorporated by and between 30 Ramland Road, LLC and Radiancy, Inc. (Orangeburg). (25)reference to Exhibit 2.1 to the Current Report on Form 8-K filed on September 4, 2015)
10.47Unprotected Tenancy
10.28Supplemental Agreement, dated September 9, 20081, 2015, among DaLian Jikang Medical Systems Import & Export Co., LTD, the Company and PhotoMedex Technology, Inc. (incorporated by and between S.A.I. Yarak Buildings and Investments Ltd. and Radiancy (Israel) Ltd. (Hod Hasharon) (25)reference to Exhibit 2.2 to the Current Report on Form 8-K filed on September 4, 2015)
10.48Amendment to Unprotected Tenancy Lease, dated as of January 20, 2008, by and between S.A.I. Yarak Buildings and Investments Ltd. and Radiancy (Israel) Ltd. (25)
10.4910.29Exclusive LicenseAsset Purchase Agreement, for Methods of Treating Diseased Tissue, dated April 1, 2012,June 22, 2015, among MELA Sciences, Inc., the Company and PhotoMedex Technology, Inc. (incorporated by reference to Exhibit 2.1 to the Current Report on Form 8-K filed on June 26, 2015)
10.30Escrow Agreement, dated June 22, 2015, among MELA Sciences, Inc., the Company and U.S. Bank National Association (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on June 26, 2015)


10.31Transition Services Agreement, dated June 22, 2015, among the Company, PhotoMedex Technology, Inc. and MELA Sciences, Inc. (incorporated by reference to Exhibit 10.2 to the Current Report on Form 8-K filed on June 26, 2015)
10.32Credit Card Receivables Advance Agreement, dated December 21, 2015, between the RegentsCompany, Radiancy, Inc., PhotoMedex Technology, Inc., Lumiere, Inc., and CC Funding, a division of Credit Cash NJ, LLC (incorporated by reference to Exhibit 10.1 to the University of California and PhotoMedex, Inc. (25)Current Report on Form 8-K filed on January 8, 2016)
10.50Non-Qualified Stock Option Agreement dated March 18, 2012 between PhotoMedex, Inc. and Dolev Rafaeli (25)
10.5110.33Non-Qualified Stock Option Agreement dated March 18, 2012 between PhotoMedex, Inc. and Dennis McGrath (25)
10.52Warrant issued March 1, 2012 to Crystal Research Associates LLC. (29)
10.53Lease Agreement, dated August 24, 2012, by and between 30 Ramland Road, LLC and Radiancy, Inc. (Orangeburg). (30) (incorporated by reference to Exhibit 10.53 to the Quarterly Report on Form 10-Q filed on November 13, 2012)
10.54Non-Qualified
10.35Stock OptionGrant Agreement, dated February 28, 2013December 22, 2017, among the Company, Dolev Rafaeli, Dennis M. McGrath and Yoav Ben-Dror (incorporated by reference to Exhibit 10.12 to the Current Report on Form 8-K filed on December 29, 2017)
10.36Registration Rights Agreement, dated December 22, 2017, among the Company, Dolev Rafaeli, Dennis M. McGrath and Yoav Ben-Dror (incorporated by reference to Exhibit 10.13 to the Current Report on Form 8-K filed on December 29, 2017)
10.37Secured Convertible Payout Note Due October 12, 2018 issued by the Company to Dolev Rafaeli on October 12, 2017 (incorporated by reference to Exhibit 10.4 to the Current Report on Form 8-K filed on October 18, 2017)
10.38Secured Convertible Payout Note Due October 12, 2018 issued by the Company to Dennis M. McGrath on October 12, 2017 (incorporated by reference to Exhibit 10.5 to the Company’s Current Report on Form 8-K filed on October 18, 2017)
10.39Secured Convertible Payout Note Due October 12, 2018 issued by the Company to Yoav Ben-Dror on October 12, 2017 (incorporated by reference to Exhibit 10.6 to the Current Report on Form 8-K filed on October 18, 2017)
10.40Security Agreement, dated October 12, 2017, by and between PhotoMedex, Inc.the Company and Dolev Rafaeli, (31)Dennis M. McGrath and Yoav Ben-Dror (incorporated by reference to Exhibit 10.7 to the Current Report on Form 8-K filed on October 18, 2017)
10.55Non-Qualified Stock Option Agreement dated February 28, 2013 between PhotoMedex, Inc. and Dennis McGrath (31)
114


10.56Quota Purchase and Sale Agreement dated May 7, 2013 by and Among Radiancy, Inc., Leo Klinger and Intervening Parties (32)
10.5710.41†Lease Agreement dated June 3, 2013 by and between Maestro Properties Limited and Photo Therapeutics, Ltd. (UK) (32)
10.58Lease Agreement dated September 23, 2013 by and between Liberty Property Limited Partnership and PhotoMedex, Inc. (33)
10.59Credit Agreement, dated as of May 12, 2014, by and among PhotoMedex, Inc., JPMorgan Chase Bank, N.A. as Administrative Agent, First Niagara Bank, N.A. and PNC Bank, National Association as Co-Syndication Agents; J.P. Morgan Securities LLC, as Lead Arranger and book runner, and the Lenders (36)
10.60Amended and Restated Employment Agreement, entered into by anddated March 10, 2015, between PhotoMedex, Inc.the Company and Dolev Rafaeli (incorporated by reference to Exhibit 10.65 to the Annual Report on August 5, 2014. (37)Form 10-K filed on March 16, 2015)
10.61
10.42†Amended and Restated Employment agreement, entered intodated March 10, 2015, between the Company and Dennis McGrath (incorporated by reference to Exhibit 10.66 to the Annual Report on Form 10-K filed on March 16, 2015)
10.43†Separation Agreement, dated December 22, 2017, between the Company and Suneet Singal (incorporated by reference to Exhibit 10.14 to the Current Report on Form 8-K filed on December 29, 2017)
10.44†Amended and restated Employment Agreement, dated October 11, 2017, by and between PhotoMedex, Inc.the Company and Dennis McGrathSuneet Singal (incorporated by reference to Exhibit 10.8 to the Current Report on August 5, 2014. (37)Form 8-K filed on October 18, 2017)
10.62Forbearance
10.45†Employment Agreement, dated August 25,2014,May 17, 2017, between the Company and Suneet Singal (incorporated by and among PhotoMedex, Inc., JPMorgan Chase Bank, N.A. as Administrative Agent, First Niagara Bank, N.A. and PNC Bank, National Association as Co-Syndication Agents; J.P. Morgan Securities LLC, as Lead Arranger and book runner, andreference to Exhibit 10.5 to the Lenders (38)Current Report on Form 8-K filed on May 19, 2017)
10.63
10.46†Amended and Restated ForbearanceSeparation Agreement, dated November 4,2014,February 12, 2018, between FC Global Realty Incorporated (Formerly: PhotoMedex, Inc.) and Stephen Johnson (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on February 16, 2018)
10.47†Separation Agreement, dated December 22, 2017, between the Company and Stephen Johnson (incorporated by reference to Exhibit 10.15 to the Current Report on Form 8-K filed on December 29, 2017)


10.48†Employment Agreement dated July 28, 2017 by and among PhotoMedex, Inc., JPMorgan Chase Bank, N.A. as Administrative Agent, First Niagara Bank, N.A.between the Company and PNC Bank, National Association as Co-Syndication Agents; J.P. Morgan Securities LLC, as Lead Arranger and book runner, andStephen Johnson (incorporated by reference to Exhibit 10.1 to the Lenders (39)Current Report on Form 8-K filed on August 3, 2017)
10.64Second
10.49†Employment Agreement, dated December 22, 2017, between the Company and Vineet P. Bedi (incorporated by reference to Exhibit 10.16 to the Current Report on Form 8-K filed on December 29, 2017)
10.50†Employment Agreement, dated December 22, 2017, between the Company and Matthew Stolzar (incorporated by reference to Exhibit 10.17 to the Current Report on Form 8-K filed on December 29, 2017)
10.51†Amended and Restated Forbearance Agreement2000 Non-Employee Director Stock Option Plan, dated February 28, 2015,as of August 3, 2010 (incorporated by and among PhotoMedex, Inc., JPMorgan Chase Bank, N.A. as Administrative Agent, First Niagara Bank, N.A. and PNC Bank, National Association as Co-Syndication Agents; J.P. Morgan Securities LLC, as Lead Arranger and book runner, andreference to Exhibit 10.44 to the Lenders (40)Annual Report on Form 10-K filed on March 31, 2011)
10.65
10.52†Amended and Restated Employment Agreement entered into2005 Equity Compensation Plan, dated as of August 3, 2010 (incorporated by and between PhotoMedex, Inc. and Dolev Rafaelireference to Exhibit 10.45 to the Annual Report on Form 10-K filed on March 10, 2015. (41)31, 2011)
10.66Amended and Restated Employment Agreement, entered into by and between PhotoMedex, Inc. and Dennis McGrath on March 10, 2015. (41)
21.114.1*
21.1*List of subsidiaries of the Company
23.1
23.1*Consent of Fahn Kanne & Co. Grant Thornton Israel
31.1
Rule 13a-14(a) Certificate31.1*Certifications of ChiefPrincipal Executive Officer Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
31.2
32.131.2*
32.1*Certification of Principal Executive Officer and ChiefPrincipal Financial and Accounting Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuantPursuant to Section 906 of the Sarbanes-Oxley Act of 2002
101.INS*
101.INS ++XBRL Instance Document
101.SCH*
101.SCH ++XBRL Taxonomy Extension Schema
101.CAL*XBRL Taxonomy Calculation Linkbase
101.DEF*XBRL Taxonomy Definition Linkbase
101.LAB*XBRL Taxonomy Label Linkbase
101.PRE*XBRL Taxonomy Presentation Linkbase

*Pursuant to Rule 406T of Regulation S-T, the Interactive Data Files on Exhibit 101 hereto are deemed not filed or part of a registration statement or prospectus for purposes of Sections 11 or 12 of the Securities Act of 1933, as amended (the "Securities Act"), are deemed not filed for purposes of Section 18 of the Exchange Act, and otherwise not subject to liability under those sections. This exhibit shall not be deemed to be incorporated by reference into any filing under the Securities Act or the Exchange Act, except to the extent that the Registrant specifically incorporates this exhibit by reference.
.
115

(1)  Filed as part of our Registration Statement on Form S-4, on October 18, 2002, and as amended.
(2)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2002.
(3)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2006.
(4)  Filed as part of our Registration Statement on Form S-1/A, on August 5, 1999.
(5)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2005.
(6)  Filed as part of our Current Report on Form 8-K, on September 13, 2004.
(7)  Filed as part of our Current Report on Form 8-K, on April 10, 2006.
(8)  Filed as part of our Definitive Proxy Statement on Schedule 14A, on November 15, 2005.
(9)  Filed as part of our Registration Statement on Form S-8, on April 13, 2005.
(10)  Filed as part of our Quarterly Report on Form 10-Q for the quarter ended June 30, 2007.
(11)  Filed as part of our Quarterly Report on Form 10-Q for the quarter ended September 30, 2007.
(12)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2007.
(13)  Filed as part of our Current Report on Form 8-K on March 5, 2009.
(14)  Filed as part of our Definitive Proxy Statement on Schedule 14A on December 18, 2008.
(15)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2008.
(16)  Filed as part of our Quarterly Report on Form 10-Q for the quarter ended June 30, 2009.
(17)  Filed as part of our Current Report on Form 8-K on January 11, 2010.
(18)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2010.
(19)   Filed as part of our Current Report on Form 8-K on July 8, 2011.
(20)   Filed as part of our Registration Statement on Form S-4, on August 12, 2011.
(21)  Filed as part of our Registration Statement on Form S-4/A, on October 5, 2011.
(22)  Filed as part of our Registration Statement on Form S-4/A, on November 2, 2011.
(23)  Filed as part of our Current Report on Form 8-K on December 16, 2011.
(24)  Filed as part of our Current Report on Form 8-K on July 2, 2007.

(25)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2011.

(26)  Filed as part of our Current Report on Form 8-K on March 23, 2010.
116

(27)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2010.

(28)  Filed as part of our Quarterly Report on Form 10-Q for the quarter ended June 30, 2012. Document
  
(29)  101.CAL ++Filed as part of our Quarterly Report on Form 10-Q for the quarter ended March 31, 2012.XBRL Taxonomy Extension Calculation Linkbase Document
  
(30)  101.DEF ++Filed as part of our Quarterly Report on Form 10-Q for the quarter ended September 30, 2012.XBRL Taxonomy Extension Definition Linkbase Document
  
(31)  101.LAB ++Filed as part of our Quarterly Report on Form 10-Q for the quarter ended March 31, 2013.XBRL Taxonomy Extension Label Linkbase Document
  
(32)  Filed as part of our Quarterly Report on Form 10-Q for the quarter ended June 30, 2013.
(33)  Filed as part of our Quarterly Report on Form 10-Q for the quarter ended September 30, 2013.
 
(34)  101.PRE ++Filed as part of LCA Vision, Inc.'s Current Report on Form 8-K on February 13, 2014.
 XBRL Taxonomy Extension Presentation Linkbase Document
(35)  Filed as part of our Annual Report on Form 10-K for the year ended December 31, 2013.
(36)  Filed as part of our Current Report on Form 8-K on May 12, 2014.
(37)  Filed as part of our Quarterly Report on Form 10-Q for the quarter ended June 30, 2014.
(38)  Filed as part of our Current Report on Form 8-K on August 25, 2014.
(39)  Filed as part of our Current Report on Form 8-K on November 4, 2014.
(40)  Filed as part of our Current Report on Form 8-K on March 3, 2015.
(41)  Filed as part of this Form 10-K.
*The certifications attached as Exhibit 32.1 accompany this Annual Report on Form 10-K pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002,

* Filed herewith

† Executive Compensation Plan or Agreement.

++XBRL (Extensible Business Reporting Language) information is furnished and shall not be deemed "filed" by the Registrant for purposes of Section 18 of the Securities Exchange Act of 1934, as amended.

Pursuant to Rule 406T of Regulation S-T, the Interactive Data Files on Exhibit 101 hereto are deemed not filed or part of a registration statement or prospectus for purposes of Sections 11 or 12 of the Securities Act of 1933, as amended (the "Securities Act"), are deemed not filed for purposes of Section 18 of the Exchange Act, and otherwise not subject to liability under those sections. This exhibit shall not be deemed to be incorporated by reference into any filing under the Securities Act or the Exchange Act, except to the extent that the Registrant specifically incorporates this exhibit by reference.

AVAILABLE INFORMATION

We are a reporting company and file annual, quarterly and special reports, proxy statements and other information with the Commission. You may inspect and copy these materials at the Public Reference Room maintained by the Commission at Room 100 F Street, N.W., Washington, D.C. 20549. Please call the Commission at 1‑800‑SEC‑0330 for more information on the Public Reference Room. You can also find our Commission filings at the Commission's website at www.sec.gov. You may also inspect reports and other information concerning us at the offices of the Nasdaq Stock Market at 1735 K Street, N.W., Washington, D.C. 20006. We intend to furnish our stockholders with annual reports containing audited financial statements and such other periodic reports as we may determine to be appropriate or as may be required by law.
117

Our primary Internet address is www.photomedex.com (this website address is not intended to function as a hyperlink and the information contained on our website is not intended to be a part of this Report). Corporate information can be located by clicking on the "Investor Relations" link in the top-middlea report for purposes of sections 11 or 12 of the page, and then clicking on "SEC Filing" in the menu. We make our periodic Commission Reports (Forms 10-Q and Forms 10-K) and current reports (Form 8-K) available freeSecurities Act of charge through our Web site as soon as reasonably practicable after they are1933, is deemed not filed electronically with the Commission. We may from time to time provide important disclosures to investors by posting them in the Investor Relationsfor purposes of section of our Web site, as allowed by Commission's rules. The information on the website listed above is not and should not be considered part of this Annual Report on Form 10-K and is intended to be an inactive textual reference only.
118

SIGNATURES
Pursuant to the requirements of Section 13 or 15(d)18 of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this Reportand otherwise is not subject to be signed on its behalf by the undersigned, thereunto duly authorized.liability under these sections.

ITEM 16.FORM 10-K SUMMARY.

None. 


FC GLOBAL REALTY INCORPORATED (FORMERLY: PHOTOMEDEX, INC.)
AND SUBSIDIARIES
   PHOTOMEDEX, INC. 
     

FC GLOBAL REALTY INCORPORATED (FORMERLY: PHOTOMEDEX, INC.) AND SUBSIDIARIES

Index to Consolidated Financial Statements

 Date:  March 16, 2015By:/s/ Dr. Dolev RafaeliPage
        Dr. Dolev Rafaeli
Chief Executive Officer and Director

Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed below by the following persons on behalf of the registrant and in the capacities and on the dates indicated.
SignatureCapacity in Which SignedDate
/s/ Lewis C. Pell
Chairman of the Board of DirectorsMarch 16, 2015
Lewis C. Pell
/s/ Dr. Yoav Ben-DrorVice Chairman of the Board of DirectorsMarch 16, 2015
Dr. Yoav Ben-Dror
/s/ Dr. Dolev RafaeliChief Executive Officer and Director (Principal Executive Officer)March 16, 2015
Dr. Dolev Rafaeli
/s/ Dennis M. McGrathPresident, Chief Financial Officer and Director (Principal Financial Officer)March 16, 2015
Dennis M. McGrath
/s/ Christina L. AllgeierChief Accounting Officer (Principal Accounting Officer)March 16, 2015
Christina L. Allgeier
/s/ James W. SightDirectorMarch 16, 2015
James W. Sight
/s/ Stephen P. ConnellyDirectorMarch 16, 2015
Stephen P. Connelly
/s/ Trevor S. HarrisDirectorMarch 16, 2015
Trevor S. Harris

119


PHOTOMEDEX, INC. AND SUBSIDIARIES
Index to Consolidated Financial Statements
Page
Report of Independent Registered Public Accounting FirmF-2
Consolidated Balance Sheets, December 31, 20142017 and 20132016F-3
Consolidated Statements of Comprehensive (Loss) Income,Loss, Years ended December 31, 2014, 20132017 and 20122016F-4
Consolidated Statements of Changes in Equity,Redeemable Convertible Preferred Stock and Stockholders’ Deficit, Years ended December 31, 2014, 20132017 and 20122016F-5
Consolidated Statements of Cash Flows, Years ended December 31, 2014, 20132017 and 20122016F-6
Notes to Consolidated Financial StatementsF-8F-8- F-47



F-1



 

REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM

Fahn Kanne & Co.

Head Office

Levinstein Tower
23 Menachem Begin Road

32 Hamasger Street

Tel-Aviv 66184,6721118, ISRAEL

P.O.B.

PO Box 36172, 61361

6136101

T +972 3 7106666

F +972 3 7106660

www.gtfk.co.il

Board of Directors and Stockholders

FC Global Realty Incorporated (Formerly: PhotoMedex Inc.

)


Opinion on the financial statements

We have audited the accompanying consolidated balance sheets of FC Global Realty Incorporated (Formerly: PhotoMedex Inc.) (a Nevada corporation) and Subsidiariessubsidiaries (the "Company"“Company”) as of December 31, 20142017 and 2013, and2016, the related consolidated statements of comprehensive (loss) income,loss, changes in equityredeemable convertible preferred stock and stockholders’ deficit, and cash flows for each of the threetwo years in the period ended December 31, 2014. 2017, and the related notes (collectively referred to as the “financial statements”). In our opinion, the financial statements present fairly, in all material respects, the financial position of the Company as of December 31, 2017 and 2016, and the results of its operations and its cash flows for each of the two years in the period ended December 31, 2017, in conformity with accounting principles generally accepted in the United States of America.

Going Concern

The accompanying financial statements have been prepared assuming that the Company will continue as a going concern. As discussed in Note 1 to the financial statements, the Company has incurred net losses for each of the years ended December 31, 2017 and 2016 and has not yet generated any revenues from real estate activities. As of December 31, 2017, there is an accumulated deficit of $134,445.  These conditions, along with other matters as set forth in Note 1, raise substantial doubt about the Company’s ability to continue as a going concern. Management’s plans in regard to these matters are also described in Note 1. The financial statements do not include any adjustments that might result from the outcome of this uncertainty.

Basis for opinion

These financial statements are the responsibility of the Company'sCompany’s management. Our responsibility is to express an opinion on thesethe Company’s financial statements based on our audits.

We are a public accounting firm registered with the Public Company Accounting Oversight Board (United States) (“PCAOB”) and are required to be independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and regulations of the Securities and Exchange Commission and the PCAOB.

We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (United States).PCAOB. Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. Anmisstatement, whether due to error or fraud. The Company is not required to have, nor were we engaged to perform, an audit includesof its internal control over financial reporting. As part of our audits we are required to obtain an understanding of internal control over financial reporting but not for the purpose of expressing an opinion on the effectiveness of the Company’s internal control over financial reporting. Accordingly, we express no such opinion.

Our audits included performing procedures to assess the risks of material misstatement of the financial statements, whether due to error or fraud, and performing procedures that respond to those risks. Such procedures included examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An auditOur audits also includes assessingincluded evaluating the accounting principles used and significant estimates made by management, as well as evaluating the overall presentation of the financial statement presentation.statements. We believe that our audits provide a reasonable basis for our opinion.


In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial position of PhotoMedex, Inc. and Subsidiaries as of December 31, 2014 and 2013, and the results of their operations and their cash flows for each of the three years in the period ended December 31, 2014, in conformity with accounting principles generally accepted in the United States of America.
We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the Company's internal control over financial reporting as of December 31, 2014, based on criteria established in the 2013 Internal Control – Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO), and our report dated March 16, 2015 expressed an unqualified opinion.


/s/ FAHN KANNE & CO. GRANT THORNTON ISRAEL

Tel-Aviv,

We have served as the Company’s auditor since 2011.

Tel Aviv, Israel

March 16, 2015

April 2, 2018



F-2

FC GLOBAL REALTY INCORPORATED (FORMERLY: PHOTOMEDEX, INC.) AND SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

(In thousands, except share and per share amounts)

  December 31, 
  2014  2013 
ASSETS    
Current assets:    
Cash and cash equivalents $10,605  $45,388 
Short term bank deposit  87   14,113 
Accounts receivable, net of allowance for doubtful accounts of $13,559 and $10,734, respectively  21,977   27,218 
Inventories, net  19,380   27,547 
   Deferred tax asset, net  762   13,041 
Prepaid expenses and other current assets  8,347   12,597 
   Assets held for sale, net  70,855   - 
Total current assets  132,013   139,904 
         
Property and equipment, net  13,802   10,489 
Patents and licensed technologies, net  8,811   10,832 
Other intangible assets, net  8,337   9,701 
Goodwill, net  24,048   24,930 
Deferred tax asset, net  567   24,039 
Other assets, net  185   213 
Total assets $187,763  $220,108 
         
LIABILITIES AND STOCKHOLDERS' EQUITY        
         
Current liabilities:        
Current portion of notes payable $704  $838 
Current portion of long term debt  38,732   10,000 
Accounts payable  12,419   14,785 
Accrued compensation and related expenses  2,622   3,230 
Other accrued liabilities  13,022   22,032 
Current portion of deferred revenues  4,480   5,961 
    Liabilities held for sale  34,497   - 
Total current liabilities  106,476   56,846 
         
Long-term liabilities:        
Notes payable, net of current maturities  25   82 
Long term debt, net of current maturities  37,768   - 
Deferred revenues, net of current portion  1,127   2,758 
Other liabilities  102   61 
Total liabilities  145,498   59,747 
         
Commitment and contingencies (Note 11)        
         
Stockholders' equity:        
    Preferred Stock, $.01 par value, 5,000,000 shares authorized; 0 shares issued and outstanding at December 31, 2014 and 2013  -   - 
Common Stock, $.01 par value, 50,000,000 shares authorized; 20,376,245 and 18,903,245 shares issued and outstanding, respectively  204   189 
Additional paid-in capital  110,391   104,954 
Retained  earnings (accumulated deficit)  (67,817)  53,679 
Accumulated other comprehensive (loss) income  (513)  1,539 
Total stockholders' equity  42,265   160,361 
Total liabilities and stockholders' equity $187,763  $220,108 

  December 31, 
  2017  2016 
ASSETS      
Current assets:        
Cash and cash equivalents $948  $2,335 
Prepaid expenses and other current assets  646   601 

Assets held for sale (Note 2 and 4)

     15,565 
Total current assets  1,594   18,501 
         
Non-current assets:        
Investment properties (Note 5)  2,600    
Investment in other company (Note 5)  1,806    
Property and equipment, net (Note 7)  5    
Other assets, net  334    
Total non-current assets  4,745    
Total assets $6,339  $18,501 
         

LIABILITIES, REDEEMABLE CONVERTIBLE PREFERRED STOCK AND STOCKHOLDERS’ DEFICIT

        
Current liabilities:        
Notes payable $778  $ 
Accounts payable  612   6,648 
Accrued compensation and related expenses (Note 10)  467   4,029 
Other accrued liabilities  2,450   6,023 

Liabilities related to assets held for sale

     3,209 
Total current liabilities  4,307   19,909 
         
Non-current liabilities:        
Option to purchase Redeemable Convertible B Preferred Stock (Note 14)  4,390    
Note payable, net of current portion (Note 12)  454    
Total non-current liabilities  4,844    
Total liabilities  9,151   19,909 
         
Commitment and contingencies (Note 13)        
         
Redeemable Convertible Preferred Stock Series B, $.01 par value; 15,000,000 shares authorized at December 31, 2017; 1,500,000 issued and outstanding at December 31, 2017, net of amount allocated to option to purchase additional shares; Aggregate liquidation preference $1,503,000 at December 31, 2017 (Note 14)  87    
         

Stockholders’ deficit (Note 14):

        
Common Stock, $.01 par value, 500,000,000 and 50,000,000 shares authorized at December 31, 2017 and 2016 respectively; 11,868,619 and 4,361,094 shares issued and outstanding at December 31, 2017 and 2016, respectively  119   44 
Preferred stock, $.01 par value, 32,000,000 shares authorized at December 31, 2017; 0 shares issued and outstanding at December 31, 2017        
Preferred A Stock $.01 par value, 3,000,000 shares authorized at December 31 ,2017; 123,668 issued and outstanding at December 31, 2017;  1    
Additional paid-in capital  132,446   118,762 
Accumulated deficit  (134,445)  (115,635)
Accumulated other comprehensive loss  (1,162)  (4,579)
Total stockholders’ deficit attributable to FC Global Realty Incorporate  (3,041)  (1,408)
Noncontrolling interest (Note 5)  142    
Total stockholders’ deficit  (2,899)  (1,408)
Total liabilities, redeemable convertible preferred stock and stockholders’ deficit $6,339  $18,501 

The accompanying notes are an integral part of these consolidated financial statements.

F-3


FC GLOABAL REALTY INCORPORATED (FORMERLY: PHOTOMEDEX, INC.) AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF COMPREHENSIVE (LOSS) INCOMELOSS

  (In thousands, except share and per share amounts)

       
  For the Year Ended December 31, 
  2017  2016 
       
Revenues: $  $ 
Cost of revenues      
Gross profit      
         
Operating expenses:        
General and administrative  10,817    

Impairment of investment in other company (Note 5)

  

862

    
   11,679    
         
Operating loss  (11,679)   
         
Revaluation of asset contribution related financial instruments, net (Note 5)  (1,392)   
Revaluation of Option to purchase redeemable convertible B preferred stock (Note 14)  (3,018)   
Interest and other financing expense, net  (267)   
Loss from continuing operations  (16,356)   
         
Discontinued operations:        
Loss from discontinued operations, net of taxes  (2,459)  (13,264)
         
Net loss including portion attributable to noncontrolling interest  

 ( 18,815

)  (13,264)
         
Loss attributable to noncontrolling interest  8    
         
Net loss attributable to FC Global Realty Incorporated $(18,807) $(13,264)
         
Basic and diluted net loss per share:        
Continuing operations $(2.96) $ 
Discontinued operations  (0.45)  (3.18)
  $(3.41) $(3.18)
         
Shares used in computing basic and diluted net loss per share  5,073,751   4,171,549 
         
Other comprehensive loss:        
Reclassification of cumulative translation adjustment $3,228  $ 
Foreign currency translation adjustments  189   (2,810)
Total other comprehensive income (loss)  3,417   (2,810)
Comprehensive loss $(15,390) $(16,074)

The accompanying notes are an integral part of these consolidated financial statements


FC GLOBAL REATLY INCORPORATED (FORMERLY: PHOTOMEDEX, INC.) AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CHANGES IN EQUITY (DEFICIT)

(In thousands, except share and per share amounts)

       
  For the Year Ended December 31, 
  2014  2013  2012 
Revenues:      
     Product sales $140,670  $209,175  $212,210 
     Services  22,871   15,489   8,441 
   163,541   224,664   220,651 
Cost of revenues:            
     Product sales  31,400   38,229   41,558 
     Services  7,219   6,806   5,084 
   38,619   45,035   46,642 
             
Gross profit  124,922   179,629   174,009 
             
Operating expenses:            
Engineering and product development  3,086   3,306   2,914 
Selling and marketing  107,169   127,528   116,487 
General and administrative  35,711   26,750   27,330 
   145,966   157,584   146,731 
(Loss) income from continuing operations before interest and other financing income (expense), net  (21,044)  22,045   27,278 
             
Interest and other financing income (expense), net  (4,387)  702   (351)
(Loss) income from continuing operations before income taxes  (25,431)  22,747   26,927 
             
Income tax expense  (36,312)  (4,370)  (4,438)
             
(Loss) profit from continuing operations  (61,743)  18,377   22,489 
             
Discontinued operations:            
Loss from discontinued operations, net of taxes of $5,496  (15,155)  -   - 
Estimated loss on sale from discontinued operations  (44,598)  -   - 
             
Net (loss) income (121,496) $18,377  $22,489 
             
Basic net (loss) income per share:            
Continuing operations (3.25) $0.90  $1.10 
    Discontinued operations  (3.16)  0.00   0.00 
  (6.41) $0.90  $1.10 
Diluted net (loss) income per share:            
Continuing operations (3.25) $0.89  $1.08 
    Discontinued operations  (3.16)  0.00   0.00 
  (6.41) $0.89  $1.08 
Shares used in computing net income (loss) per share:            
Basic  18,940,355   20,454,970   20,355,520 
    Diluted  18,940,355   20,657,240   20,764,354 
             
Other comprehensive (loss) income:            
Foreign currency translation adjustments (2,052) $678  $859 
             
Comprehensive (loss) income (123,548) $19,055  $23,348 
             
amounts)

  Redeemable Convertible Preferred Stock  Stockholders’ deficit 
  Series B  Common Stock  Series A Preferred Stock  Additional Paid-In  

Accumulated

  Accumulated Other Comprehensive  Noncontrolling    
  Shares  Amount  Shares  Amount  Shares  Amount  Capital  Deficit  Loss  Interest  Total 
                                             
BALANCE, DECEMBER 31, 2015        4,398,344  $44        $116,793   ($102,371)  ($1,769)    $12,697 
Stock-based compensation related to stock options and restricted stock                    1,969            1,969 
Restricted stock canceled        (37,250)                        
Foreign currency translation adjustment                          (2,810)     (2,810)
                                             
Loss                       (13,264)        (13,264)
BALANCE, DECEMBER 31, 2016        4,361,094  $44        $118,792   ($115,635)  ($4,579)     ($1,408)
                                             
Stock-based compensation related to stock options and restricted stock                    1,466            1,466 
                                             
Common shares issued for asset contribution (Note 5)        879,234   9         1,266            1,275 
                                             
Preferred A stock issued for asset contribution (Note 5 )              123,668   1   4,482            4,483 
Common shares issued for Note Payout (Note 14)          5,628,291   56          5,570              5,626 
Common shares issued for severance (Note 14)        1,000,000   10         900            910 
Issuance of series B redeemable convertible preferred stock and embedded option, net of stock issuance costs of $42  1,500,000                               
Amortization of discount related to written call option (Note14)    $84                            
Accretion of dividend (Note 14)    $3                  

(3

        (3
Noncontrolling interest from asset acquisition                             150   150 
Reclassification of cumulative translation adjustment                          3,228      3,228 
Foreign currency translation adjustment                                 189      189 
Net Loss                       (18,807)     (8)  (18,815)
BALANCE, DECEMBER 31, 2017  1,500,000  $87   11,868,619  $119   123,668  $1  $132,446   ($134,445)  ($1,162) $142   ($2,899)

The accompanying notes are an integral part of these consolidated financial statements.


F-4

FC GLOBAL REALTY INCORPORATED (FORMERLY: PHOTOMEDEX, INC.) AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CHANGES IN EQUITY

CASH FLOWS

(In thousands)


  Common Stock  Additional Paid-In  Treasury  
Retained Earnings
(Accumulated
  Accumulated Other Comprehensive   
  Shares  Amount  Capital  stock  Deficit)  (Loss) Income  Total 
BALANCE, DECEMBER 31, 2011  18,821,728  $188  $97,972  $(250) $12,813  $2  $110,725 
Issuance of warrants to consultants for services  -   -   98   -   -   -   98 
Stock-based compensation - grants of common stock  30,000   -   405   -   -   -   405 
Stock-based compensation related to stock options and restricted stock  -   -   5,709   -   -   -   5,709 
Stock options issued to consultants for services  -   -   83   -   -   -   83 
Issuance of common stock, net  3,023,432   30   37,484   -   -   -   37,514 
Repurchase and retirement of common stock  (842,961)  (9)  (10,747)  -   -   -   (10,756)
Exercise of stock options  10,048   -   67   -   -   -   67 
Warrants exercised  17,756   1   133   -   -   -   134 
Retirement of treasury stock (16,056 shares)  (16,056)  -   (250)  250   -   -   - 
Other comprehensive income  -   -   -   -   -   859   859 
Net income  -   -   -   -   22,489   -   22,489 
BALANCE, DECEMBER 31, 2012  21,043,947   210   130,954   -   35,302   861   167,327 
Stock-based compensation related to stock options and restricted stock  -   -   4,892   -   -   -   4,892 
Stock options issued to consultants for services  -   -   93   -   -   -   93 
Repurchase and retirement of common stock  (2,144,452)  (21)  (31,008)  -   -   -   (31,029)
Exercise of stock options  3,750   -   23   -   -   -   23 
Other comprehensive income  -   -   -   -   -   678   678 
Net income  -   -   -   -   18,377   -   18,377 
BALANCE, DECEMBER 31, 2013  18,903,245   189   104,954   -   53,679   1,539   160,361 
Stock-based compensation related to stock options and restricted stock  -   -   4,862   -   -   -   4,862 
Stock options issued to consultants for services  1,663   -   76   -   -   -   76 
Issuance of common stock, net  645,000   7   1,406   -   -   -   1,413 
Restricted stock issued, net of payroll taxes paid  826,337   8   (988)  -   -   -   (980)
Issuance of warrants  -   -   81   -   -   -   81 
Other comprehensive loss  -   -   -   -   -   (2,052)  (2,052)
Net loss  -   -   -   -   (121,496)  -   (121,496)
BALANCE, DECEMBER 31, 2014  20,376,245  $204  $110,391  $-  $(67,817) $(513) $42,265 

thousands)

  For the Year Ended December 31, 
  2017  2016 
Cash Flows From Operating Activities:        
Net loss  ($16,966) $ 
Adjustments to reconcile loss to net cash provided by (used in) operating activities related to continuing operations:        
Depreciation and amortization  297    
Impairment of investment in other company  862    
Deferred income taxes  66    
Stock-based compensation  655    
Capital loss from sale of assets  2,567    
Revaluation of asset contribution related financial instruments, net (Note 5)  1,392    

Revaluation of option to purchase redeemable convertible B preferred stock (Note 14)

  2,890    
Issuance costs allocated to Option to purchase redeemable convertible B preferred stock (Note 14)  42    
Changes in operating assets and liabilities:        
Accounts receivable  1,518    
Prepaid expenses and other assets  2,072    
Accounts payable  (2,134)   
Accrued compensation and related expenses  2,936    
Other accrued liabilities  (2,906)   
Amortization of discount on mezzanine  84     
Adjustments related to continuing operations  10,341    
Adjustments related to discontinued operation  (2,673)  358 
         

Net cash provided by (used in) operating activities

  (9,298)  358 
         
Cash Flows From Investing Activities:        
Direct expenses related to asset acquisition (Note 5)  (283)   
Purchases of property and equipment  (22)   
Stock based compensation  10     
Payment of note receivable  (159)   
Net cash provided by investing activities – continuing operation  454    
Net cash provided by investing activities – discontinued operations  7,251   2,148 
Net cash provided by investing activities  6,797   2,148 

The accompanying notes are an integral part of these consolidated financial statements.

F-5


PHOTOMEDEX, INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

(In thousands)

  For the Year Ended December 31, 
  2014  2013  2012 
Cash Flows From Operating Activities:      
Net (loss) income (121,496) $18,377  $22,489 
Adjustments to reconcile net (loss) income to net cash (used in) provided by operating activities:            
Depreciation and amortization  6,912   6,119   5,611 
Provision for doubtful accounts  7,661   5,958   4,629 
Deferred income taxes  35,699   2,589   (2,330)
Stock-based compensation  4,938   4,985   6,197 
Amortization of bank debt issue costs and discount  2,358   -   - 
Loss on disposal of property and equipment  (10)  -   - 
Changes in operating assets and liabilities:            
Accounts receivable  (2,718)  (13,944)  (11,254)
Inventories  7,967   (4,967)  (3,195)
Prepaid expenses and other assets  2,378   843   (8,583)
Accounts payable  (2,244)  4,658   1,787 
Accrued compensation and related expenses  (588)  733   (1,316)
Other accrued liabilities (see Note 9)  (8,839)  (444)  5,719 
Other liabilities  -   -   (1)
Deferred revenues  (3,083)  130   5,243 
Net cash (used in) provided by operating activities – continuing operations  (71,065)  25,037   24,996 
Net cash provided by operating activities – discontinued operations  46,894   -   - 
Net cash (used in) provided by operating activities  (24,171)  25,037   24,996 
             
Cash Flows From Investing Activities:            
Purchases of property and equipment  (251)  (943)  (573)
Lasers placed into service  (6,746)  (5,476)  (3,221)
Proceeds from (investments in) short-term deposit  14,026   3,887   (18,000)
Proceeds on sale of property and equipment  20   -   - 
Acquisition, net of cash received  (77,510)  84   - 
Net cash used in investing activities – continuing operations  (70,461)  (2,448)  (21,794)
Net cash used in investing activities – discontinued operations  (5,218)  -   - 
Net cash used in investing activities  (75,679)  (2,448)  (21,794)














  For the Year Ended December 31, 
  2017  2016 
       
Cash Flows From Financing Activities:        
Proceeds from issuance of redeemable  preferred B stock and embedded option, net of issuance cost of $42 (Note 14)  1,458    
Proceeds from note payable  111    
Net cash provided by financing activities –continuing operation  1,569    

Net cash provided by (used in) financing activities – discontinued operations

  (663)  (684)
Net cash provided by (used in) financing activities  906   (684)
         
Effect of exchange rate changes on cash  208   (2,789)
Change in cash and cash equivalents  (1,387)  (967)
Cash and cash equivalents at the beginning of year  2,335   3,302 
         
Cash and cash equivalents at the end of year $948  $2,335 
         
Supplemental disclosure of non-cash activities:        
Cash paid for income taxes $36  $203 
Cash paid for interest $126  $281 
Contribution of investment property and investment in other company against stock issue, financial assets related to future mandatory asset contribution and financial liabilities for optional asset acquisition (Note 5) $4,836    
Conversion of Payout Notes into shares of common stock $5,626    

The accompanying notes are an integral part of these consolidated financial statements.

F-6



FC GLOBAL REALTY INCORPORATED (FORMERLY: PHOTOMEDEX, INC. AND SUBSIDIARIES

)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS OF CASH FLOWS

(In thousands, except share and per share amounts.)

)


  For the Year Ended December 31, 
  2014  2013  2012 
       
Cash Flows From Financing Activities:      
Repurchase of common stock  -   (31,029)  (10,756)
Proceeds from issuance of common stock, net  1,413   -   37,514 
Issuance of warrants  81   -   98 
Issuance of restricted stock, net of taxes  (980)  -   - 
Proceeds from option exercises  -   23   67 
Proceeds from warrant exercises  -   -   134 
Proceeds from issuance of debt  85,000   10,000   - 
Repayment of debt  (18,500)  -   - 
Payments on notes payable  (838)  (623)  (465)
Repayment of long-term debt  -   (43)  (2,000)
Net cash provided by (used in) financing activities – continuing operations  66,176   (21,672)  24,592 
Net cash (used in) financing activities – discontinued operations  (523)  -   - 
Net cash (used in) provided by financing activities  65,653   (21,672)  24,592 
             
Effect of exchange rate changes on cash  (586)  123   5 
Net (decrease) increase in cash and cash equivalents  (34,783)  1,040   27,799 
Cash and cash equivalents, beginning of year  45,388   44,348   16,549 
             
Cash and cash equivalents, end of year $10,605  $45,388  $44,348 
             
Supplemental information:            
             
Cash paid for income taxes $1,041  $7,233  $12,976 
Cash paid for interest $2,216  $13  $79 
             














The accompanying notes are an integral part of these consolidated financial statements.
F-7

Note 1
The Company and Summary of Significant Accounting Policies:
The Company:
Background

Background:

FC Global Realty Incorporated (formerly PhotoMedex, Inc.) (and its subsidiaries) (the "Company"“Company” or “FCRE”), re-incorporated in Nevada on December 30, 2010, originally formed in Delaware in 1980, is, since earlier in 2017, a real estate development and asset management company concentrated primarily on investments in high quality income producing assets, hotel and resort developments, residential developments and other opportunistic commercial properties.

Under its previous name, PhotoMedex, Inc., the Company was, until the recent sale of the Company’s last significant business unit (its consumer products division which was sold to ICTV Brands, Inc. on January 23, 2017), as described below and in other sections of this report, a Global Skin Health company providing integrated disease management and aesthetic solutions to dermatologists, professional aestheticians and consumers. The Company providesprovided proprietary products and services that addressaddressed skin diseases and conditions including psoriasis, vitiligo, acne, actinic keratosis (a precursor to certain types of skin cancer), photo damage and unwanted hair.

On December 13, 2011,hair.

Starting in August 2014, the Company closedbegan to restructure its operations and redirect its efforts in a manner that management expected would result in improved results of operations and address certain defaults in its commercial bank loan covenants. As part of such redirected efforts, management continued its comprehensive efforts to minimize the merger with Radiancy, Inc. Immediately following the reverse merger, the pre-reverse merger shareholders of PhotoMedex, Inc. ("Pre-merged PhotoMedex") collectively owned approximately 20% of the Company's outstanding common stock,Company’s operational costs and the former Radiancy, Inc. stockholders owned approximately 80% of the Company's outstanding common stock.

On March 3, 2014, PhotoMedex' wholly-owned subsidiary, Radiancy, Inc., formed a wholly-owned subsidiary in Hong Kong, Radiancy (HK) Limited, through whichcapital expenditures. During this time the Company has startedalso sold off certain business units and product lines to directly market certainsupport this restructuring, and on January 23, 2017, sold the last remaining major product line, its consumer products division.

As a result of the Contribution Agreement (see also Note 5), the Company has primarily become a real estate asset management and servicesdevelopment company for the purpose of investing in a diversified portfolio of quality commercial and residential real estate properties and other real estate investments located both throughout the United States.

Resignation and Appointment of Officers and Directors:

Pursuant to patientsthe Contribution Agreement and consumersPurchase Agreement (see also Notes 5 and 14, respectively), there were changes to the Company’s named executive officers and its Board of Directors that were made on May 17, 2017 and December 22, 2017.

Expansion of Company’s Board of Directors quorum:

At the Initial Date of the First Contribution under the Contribution Agreement (see also Note 5), the Company’s Board of Directors was expanded, so that the Board of Directors consists of seven persons, of whom (i) three were designated by the Company’s departing board, (ii) three were designated by Contributor Parent; and (iii) one (the “Nonaffiliated Director”) was selected by the other six directors.

In March 2018, two members of the Company’s Board of Directors resigned from their position as directors and Opportunity Fund I-SS, LLC has notified the Company that it exercised its right under the Purchase Agreement (see also Note 14) to appoint two replacement directors to the Company’s Board of Directors (see also Note 17).

Special Meeting of Stockholders

Following the Initial Closing of the First Contribution under the Contribution Agreement (see also Note 5), the Company was required to file a proxy statement and hold a special meeting of its stockholders to authorize and approve the following matters:

an increase in the number of authorized shares of common stock, $.01 par value per share, of the Company from 50,000,000 shares to 500,000,000 shares and increase the number of authorized shares of preferred stock, $.01 par value per share, of the Company from 5,000,000 shares to 50,000,000 shares;

the issuance to the Contributor or its designee or designees of the Company’s common and/or preferred shares in exchange for the contributed assets, and the issuance of the Warrant and, upon exercise of the Warrant, the underlying shares of the Company’s Common Stock in exchange for the contribution of the optional property interests, if any are made;

the amendment and restatement of the Articles of Incorporation of the Company;

the approval of the issuance of the Payout Notes and the issuance of the Company’s Common Stock upon conversion thereof; and

the election of a new Board of Directors as set forth above in Resignation and Appointment of Officers and Directors in this report.

The Annual Meeting of Shareholders was convened on September 14, 2017, then adjourned and reconvened on October 12, 2017, at which meeting all of the proposals specified in selected marketsthe Company’s Definitive Proxy and further described in that region.

On March 5, 2014, PhotoMedex formedProxy and in this filing were approved by the stockholders.

Liquidity and Going Concern:

As of December 31, 2017, the Company had an accumulated deficit of $134,445 and the Company incurred a wholly-owned subsidiary in India, PhotoMedex India Private Limited, through whichnet loss attributable to FC Global Realty Incorporated, for the year ended December 31, 2017 of $18,807. Subsequent to the sale of the Company’s last significant business unit, the consumer products division as described above, and to date, the Company has dedicated most of its financial resources to general and administrative expenses.

As of December 31, 2017, the Company’s cash and cash equivalents amounted to $948. While the Company is directly marketinga party to a Securities Purchase Agreement with Opportunity Fund I-SS, LLC, and has raised certain productsfunds under that agreement in both 2017 and services to patients and consumers in selected markets in that country.

On May 12, 2014, PhotoMedex completed2018 through the acquisition of 100%date of the shares of LCA-Vision Inc. ("LCA-Vision" or "LCA"), which was a publicly–traded Delaware corporation. LCA is a provider of fixed-site laser vision corrections services at its LasikPlus® vision centers. Through this acquisition,financial statements, Opportunity Fund has no obligation to continue to invest in the Company, added an additional operating segment to its organization.and there are restrictions placed by Opportunity Fund on the use of these funds. The Company plannedhas historically financed its activities with cash from operations, the private placement of equity and debt securities, borrowings under lines of credit and, in the most recent periods with sales of certain assets and business units. The Company will be required to beginobtain additional liquidity resources in order to directly market certainsupport its operations.

At this time, there is no guarantee that the Company will be able to obtain an adequate level of financial resources required for the short and long-term support of its existing products from these centers.operations or that the Company will be able to obtain additional financing as needed, or meet the conditions of such financing, or that the costs of such financing may not be prohibitive.

These conditions raise substantial doubt about the Company’s ability to continue as a going concern. The results of operations of LCA-Vision have been included from May 13, 2014 through December 31, 2014 in the Company'saccompanying consolidated financial statements as a discontinued operation. (See do not include any adjustments to reflect the possible future effects on recoverability of assets and classification of liabilities that may result from the outcome of this uncertainty.

As discussed in Note 3, Acquisition of LCA-Vision Inc.).

On August 18, 2014, the Company formed a wholly-owned subsidiary in Korea, PhotoMedex Korea Limited, through which the Company plans to directly market certain products and services to patients and consumers in selected markets in that country.
On4, on January 31, 2015,23, 2017, the Company sold 100%its consumer products division to ICTV Brands, Inc., for a total selling price of $9.5 million. The Company collected $5 million of that purchase price; the sharesremaining amount of LCA-Vision Inc. up to $4.5 million was to be payable through a contingent royalty on the sale of consumer products by ICTV Brands. As discussed in further detail below, that royalty arrangement was settled in July 2017 for $40a payment of $2 million in cash. Excluding working capital adjustments and professional fees,to the Company.

On July 12, 2017 the Company, realized net proceeds of approximately $36.5 million. The LCA-Vision assetsalong with its subsidiaries Radiancy, Inc. (“Radiancy”), Photo Therapeutics Ltd. (“PHMD UK”), and liabilities are considered to be held for sale as of December 31, 2014. For the statement of operations, the activity related to LCA is captured as discontinued operations. (See Note 2,Discontinued Operations.)

On May 12, 2014,Radiancy (Israel) Limited (“Radiancy Israel” and together with the Company, entered into an $85 million senior secured credit facilities ("Radiancy and PHMD UK the Facilities") with JP Morgan Chase ("Chase") which included“Sellers” and each individually a $10 million revolving credit facility and a $75 million four-year term loan. The facilities were utilized to refinance the existing term debt with Chase, fund the acquisition of LCA and for working capital and other general corporate purposes.
There are financial covenants including a maximum leverage covenant and a minimum fixed charge covenant, which the Company must maintain. These covenants will be determined quarterly based on a rolling past four quarters of financial data. As of June 30, 2014 the Company failed to meet the financial covenants and as of December 31, 2014, the Company continued to fail to meet these covenants and remains in default.
Effective February 28, 2015, the Company“Seller”) entered into a Second AmendedTermination and Restated ForbearanceRelease Agreement (the "Second Amended Forbearance Agreement"“Release”) withbetween the lenders (the "Lenders"Sellers and ICTV Brands Inc. (“ICTV”) thatand its subsidiary ICTV Holdings, Inc. (“ICTV Holdings”). The Sellers, ICTV and ICTV Holdings are partiesreferred to herein individually as a “Party” and collectively as the “Parties.”

Under the terms of the Release, the Asset Purchase Agreement among the Parties, dated October 4, 2016, as amended by the First Amendment to the CreditAsset Purchase Agreement, dated May 12, 2014,January 23, 2017 (as so amended, the “Purchase Agreement”), is terminated and of no further force and effect, except for certain surviving rights, obligations and covenants described in the Release. Pursuant to the Release, each of the Sellers, on one hand, and ICTV and ICTV Holdings, on the other hand, fully release, forever discharge and covenant not to sue any other Party, from and with JP Morgan Chase, as Administrative Agent forrespect to any and all past and present claims arising out of, based upon or relating to the Lenders.

F-8

Purchase Agreement (other than the surviving covenants described in the Purchase Agreement) or the transactions contemplated thereby.


Pursuant to the terms of the Second Amended Forbearance Agreement,Release, ICTV was required to pay to the LendersCompany, within 3 business days of the date of the Release, $2,000 in cash and in immediately available funds (the “Payment”). Subject to this Payment, neither ICTV nor ICTV Holdings shall have agreedany further royalty or other payment obligations under the Purchase Agreement. The Company received $2,000 on July 13, 2017.

As partial consideration for the releases provided by ICTV Holdings to forbearthe Sellers pursuant to the Release and in accordance with the terms therein, on July 12, 2017, the Sellers and ICTV Holdings entered into a Bill of Sale and Assignment (“Bill of Sale”), which provides that each Seller sell, assign, transfer, convey and deliver to ICTV Holdings, and ICTV Holdings purchase and accept from exercising their rightseach Seller, all of the right, title and remediesinterest, legal or equitable, of each such Seller in and to a deposit in the amount of $210 held by a consumer division vendor, Sigmatron International, Inc. (“Sigmatron”), pursuant to an arrangement between one or more of the Sellers and Sigmatron.

As the total selling price has been adjusted to an amount that was less than the aggregate carrying amount of the assets held for sale, the Company recorded a loss from sale of asset in an amount of $4,652 (net of a gain of $3,228 with respect to accumulative translation adjustment that was reclassified from accumulated other comprehensive income to earnings). This loss is included in discontinued operations for each period.

As discussed in Note 5, on March 31, 2017, the Specified EventsCompany entered into a Contribution Agreement with First Capital Real Estate Operating Partnership, L.P., and its parent, First Capital Real Estate Trust Incorporated, under which certain real estate investment properties were to be contributed to the Company in three stages in exchange for the issuance of Default from August 25, 2014 until April 1, 2016, or earlier if an eventCompany stock. The closing of default occurs (the "Forbearance Period"). Chasethe First Contribution under this transaction occurred on May 17, 2017, and consideration transferred consisted of shares of common and preferred stock.As of December 31, 2017, neither the Secondary nor the Optional Contribution were made and the Lenders agreedContribution Agreement was terminated at that date.

As discussed in Note 14, on December 22, 2017, the Company shall not be obligatedentered into a Purchase Agreement with Opportunity Fund I-SS, LLC, a Delaware limited liability company (the “Investor”), pursuant to paywhich the principal amounts set forthInvestor may invest up to $15 million ($1.5 million out of which, net of expenses was received on December 22, 2017) in the Credit AgreementCompany in a series of closings, in exchange for any date identified therein duringwhich the period beginning on February 28, 2015 and ending on the endInvestor will receive shares of the Forbearance Period (the "Effective Period"Company’s newly designated Series B Preferred Stock (“Convertible Redeemable Series B Preferred Stock” or “Series B Shares”), and that any failure to do so shall not constitute at a default or eventpurchase price of default. Instead, the Lenders and the Company agreed that the Company would make prepayments against the Term Loan of $250,000$1.00 per share.

As discussed in Note 17, on the first business day of each month during the Forbearance Period, which will be applied in direct order of maturity. The Company also agreed that, on or before the fifth calendar day of each month, the Company would pay against the Term Loan $125,000 to the extent that the cash-on-hand exceeds $5 million, and 100% of the cash-on-hand in excess of $7 million, also to be applied to the Term Loan in inverse order of maturity.

Under the provisions of the Second Amended Forbearance Agreement, the Company will not have to comply with certain financial covenants contained in the Credit Agreement for the Forbearance Period, and that any failure to do so shall not constitute a default or event of default.  However, the Company will have to meet certain minimum EBITDA targets (as defined in the forbearance agreement) for the quarters ending March 31, 2015, June 30, 2015, September 30, 2015 and December 31, 2015.
Pursuant to the Second Amended Forbearance Agreement, all loans under the Facilities shall, beginning November 1, 2014, bear interest at the CB Floating Rate (as defined in the Credit Agreement) plus 4.00%. Additionally, following the occurrence and continuance of any default or event of default (other than a Specified Event of Default), the Company's obligations under the Facilities shall, at the option of Chase and the Lenders, bear interest at the rate of 2.00% plus the rate otherwise in effect.
The Company and its subsidiaries have also agreed not to pay in cash any compensation to either the Company's Chief Executive Officer or President that is based on a percentage of sales or another metric other than those officer's base salary, perquisites and standard benefits provided to or on behalf of those executives under the terms of their employment agreements. Those payments may be accrued or deferred and paid in cash only after the repayment of the Facilities in full.
The Company has agreed to provide, on or before May 29, 2015, a strategic business plan for the overall direction of the Company's and its subsidiaries' businesses, including projected income statements, balance sheets, schedules of cash receipts and cash disbursements, payments and month-end balances, and detailed notes and assumptions, projected on a monthly basis through April 1, 2016. The Company has also agreed to provide quarterly updates to that plan by August 31, 2015, November 30, 2015 and February 29, 2016.
The Company continues to retain the services of both Getzler Henrich & Assoc. LLC, a third-party independent business advisor, as well as Canaccord Genuity, Inc., a banking and financial services company, and has also retained the services of Nomura Securities International, Inc., also a banking and financial services company. During the Forbearance Agreement and amendments,January 24, 2018, the Company and these advisors willthe Investor completed a second closing under the Purchase Agreement, pursuant to which the Investor provided approximately $2,225 to the Company, net of expenses, in exchange for 2,225,000 shares of the Company’s Convertible Redeemable Series B Preferred Stock. While the Company is a party to a Securities Purchase Agreement with Opportunity Fund I-SS, LLC, and has raised certain funds under that Agreement, Opportunity Fund has no obligation to continue to prepare and distribute offering memoranda and other marketing materials to prospective lenders with regard to a proposed credit facility for the Company, the proceeds of which would beinvest in an amount sufficient to repay in full and in cash the Company's remaining obligations under the Facilities, and to explore other strategic alternatives. The closing of any such refinancing or alternative arrangement would occur no later than the end of the Forbearance Period.
The Company agreed to limit certain capital expenditures to $100,000 per quarter, except for those involving the Company's XTRAC® or VTRAC® medical devices, and will not make investments or acquire any other interests in affiliated companies except as agreed to by the Lenders.
F-9


As consideration for the Lender's entry into the Second Amended Forbearance Agreement, the Company has agreed to pay the Lenders certain forbearance fees (the "Forbearance Fees"), which are earned on the last business day of each of the specified months: for May and June 2015, $750,000 each month; for July through September 2015, $1,000,000 each month; for October through December 2015, $1,250,000 each month; and for January through March 2016, $1,500,000 each month.  However, should the Company complete a capital transaction acceptable to the Lenders that reduces the then-outstanding principal balance of the Term Loan to less than $10 million and repays all Forbearance Fees accrued and unpaid to that date, the monthly Forbearance Fee for the remainder of the Forbearance Period shall be earned and accrued in an amount that is 50% of the amount specified for each of the remaining months. In addition, the $500,000 Forbearance Fee set forth in Section 4.10(b) of the Amended Forbearance Agreement remains due and payable to the Lenders on the earlier of the Expiration Date or the Termination Date of the Forbearance Period. 
The Second Amended Forbearance Agreement is also subject to customary covenants, including limitations on the incurrence of or payments on indebtedness to other persons or entities and requirements that the Company provide periodic financial information and information regarding the status of outstanding litigation involving the Company, and its subsidiariesthere are restrictions placed by Opportunity Fund on the use of these funds.

Note 2

Discontinued Operations:

As this business was a substantial business unit of the Company, and as such the sale brings a strategic shift in focus of management. The Company accordingly classified this former business as held for sale and discontinued operations in accordance with ASC Topic 360.

The accompanying consolidated financial statements as of and for the year ended December 31, 2016 have been retrospectively adjusted to reflect the operating results and balance sheet items of the Consumer business as discontinued operations separately from continuing operations. Also, as of December 31, 2016, balance sheet items related to the Lenders.Consumer business were presented as assets held for sale. The Company recognized a loss of $13,264, on the sale of the discontinued operations in the year ended December 31, 2016, which represents the difference between the adjusted net purchase price and the carrying value of the disposal group.


The following is a summary of assets and liabilities held for sale in the consolidated balance sheet as of December 31, 2016, which has been retrospectively adjusted to reflect the assets and liabilities of the skin health business as discontinued operations:

  December 31, 2016 
ASSETS    
Current assets:    
Cash and cash equivalents $ 
Restricted cash deposits  342 
Accounts receivable, net of allowance for doubtful accounts of $1,192  4,125 
Prepaid expenses and other current assets  2,652 
   Assets held for sale (Note 4)  8,362 
Total current assets  15,481 
     
Non-current assets:    
   Property and equipment, net (Note 7)  77 
   Other assets, net  7 
Total non-current assets  84 
Total assets $15,565 
     
LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)    
Current liabilities:    
Other accrued liabilities  2,068 
Deferred revenues  1,141 
Total current liabilities $3,209 
     
Total net assets of discontinued operation $12,356 

The following is a summary of loss from discontinued operations for the year ended December 31, 2017 and 2016:

  For the Year Ended December 31, 
  2017  2016 
       
Revenues: $3,880  $38,397 
         
Cost of revenues  100   8,086 
         
Gross profit  3,780   30,311 
         
Operating expenses:        
Engineering and product development  143   1,249 
Selling and marketing  620   21,729 
         
General and administrative  2,342   13,233 
Impairment loss     3,518 
Other income, net  (1,504)   
Loss on sale of assets  4,652   2,574 
   6,253   42,303 
Loss before interest and other financing expense, net  (2,473)  (11,992)
         
Interest and other financing expense, net     (385)
Loss before income taxes  (2,473)  (12,377)
         
Income tax expense (benefit)  (14)  762 
         
Loss from discontinuing operations  (2,459)  (13,139)
         
    Loss from discontinued operations, net of taxes     (125)
         
Loss ($2,459) ($13,264)

Note 3

Summary of Significant Accounting Policies:

Accounting Principles

The consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America ("(“US GAAP"GAAP”). Certain reclassifications from the prior year presentation have been made to conform to the current year presentation. These reclassifications did not have material impact on the Company'sCompany’s equity, net assets, results of operations or cash flows.

Principles of Consolidation

The consolidated financial statements include the accounts of the Company and the wholly and majority ownedmajority-owned subsidiaries. All significant intercompany balances and transactions have been eliminated in consolidation.

Entities in which the Company directly or indirectly owns more than 50% of the outstanding voting securities, and for which other interest holders do not possess the right to affect significant management decisions, are generally accounted for under the voting interest consolidation method of accounting. Participation of other interest holders in the net assets and in the earnings or losses of a consolidated subsidiary is reflected in the line items “Noncontrolling Interest” in the Company’s consolidated balance sheets and “net income (loss) attributable to the noncontrolling interest” in the Company consolidated statements of comprehensive loss. Noncontrolling interest adjusts the Company’s consolidated results of operations to reflect only the Company’s share of the earnings or losses of the consolidated subsidiary.

Any changes in the Company’s ownership interest in a consolidated subsidiary, through additional equity issuances by the consolidated subsidiary or from the Company acquiring the shares from existing shareholders, in which the Company maintains control is recognized as an equity transaction, with appropriate adjustments to both the Company’s additional paid-in capital and the corresponding noncontrolling interest.

Held for Sale Classification and Discontinued Operations

A

Under ASC 205 “Presentation of Financial Statement - Discontinued Operations”, a disposal group is reported as held for sale when management has approved or received approval to sell and is committed to a formal plan, the disposal group is available for immediate sale, the business is being actively marketed, the sale is anticipated to occur during the next 12 months and certain other specified criteria are met. A disposal group classified as held for sale is recorded at the lower of its carrying amount or estimated fair value less cost to sell. If the carrying value of the business exceeds its estimated fair value less cost to sell, a loss is recognized. However, when a disposal group meets the held for sale criteria, the Company first evaluates whether the carrying amounts of the assets not covered by ASC 360-10 included in the disposal group (such as goodwill) are required to be adjusted in accordance with other applicable GAAP before measuring the disposal group at fair value less cost to sell.

Assets and liabilities related to a disposal group classified as held for sale are segregated in the consolidated balance sheet in the period in which the business is classified as held for sale.

Operations of a disposal group are reported as discontinued operations if the disposal group is classified as held for sale the(see also Note 2 and 4).

Only disposal of a component of an entity or a group of components of an entity that represents a strategic shift that has or will have a major effect on an entity’s operations and cash flows of the business have been or willfinancial results shall be eliminated from our ongoing operationsreported as a result of a disposal transaction and we will not have any significant continuing involvement in the operations of the business after the disposal transaction. discontinued operations.

The results of discontinued operations are reported in discontinued operations in the consolidated statement of operationscomprehensive loss for current and prior periods commencing in the period in which the business meets the criteria of a discontinued operation, and include any gain or loss recognized on closing or adjustment of the carrying amount to fair value less cost to sell. Depreciation is not recorded on assets of a business while it is classified as held for sale.

At December 31, 2014, held for sale assets and liabilities consisted of LCA operating segment, and its results of operations are presented as discontinued operations in the consolidated statement of operations (see alsoNote 2,Discontinued Operations).
F-10


Use of Estimates

The preparation of the consolidated financial statements in conformity with accounting principles generally accepted in the United States ("US GAAP")GAAP requires management to make estimates and assumptions that affect amounts reported of assets and liabilities at the date of the financial statements and the reported amount of revenues and expenses during the reporting periods. Actual results could differ from those estimates and be based on events different from those assumptions. As part of December 31, 2014,these financial statements, the more significant estimates include (1) revenue recognition, including provision for sales returnstock-based compensation; (2) identification of and valuation allowancesmeasurement of accounts receivable; (2) valuation allowanceinstruments in equity transactions; (3) impairment of deferred tax assetsinvestment properties and uncertaintyinvestment in tax positions;other company; (4) evaluation of going concern; and (3) stock based compensation.(5) contingencies.


Functional Currency

The currency of the primary economic environment in which the operations of the Company its U.S. subsidiaries and Radiancy Ltd., its subsidiary in Israel, are conducted is the US dollar ("(“$" or "dollars"“Dollars”). Thus, the functional currency of the Company and itssuch subsidiaries (other than the foreign subsidiariesUK subsidiary as mentioned below) is the dollar (which is also the reporting currency of the Group). The operations of the other foreign subsidiaries are eachUK subsidiary is conducted in the local currency of the subsidiary. These currencies include:this subsidiary, which is Great Britain Pounds (GBP).

In accordance with ASC 830,“Foreign Currency Matters”, Brazilian Real (BRL), Hong Kong Dollar (HKD), Columbian Peso (COP) and Indian Rupee (INR). Substantially all of the Group's revenues are derived in dollars or in other currencies linked to the dollar. Purchases of most materials and components are carried out in, or linked to the dollar.

Balancesbalances denominated in, or linked to, foreign currencies are stated on the basis of the exchange rates prevailing at the balance sheet date. For foreign currency transactions included in the statement of comprehensive income (loss),loss, the exchange rates applicable to the relevant transaction dates are used. Transaction gains or losses arising from changes in the exchange rates used in the translation of such balances are carried to financing income or expenses.

Assets and liabilities of foreign subsidiaries, whose functional currency is the local currency, are translated from its respective functional currency to U.S. dollars at the balance sheet date exchange rates. Income and expense items are translated at the average rates of exchange prevailing during the year. Translation adjustments are reflected in the consolidated balance sheets as a component of accumulated other comprehensive income or loss. Deferred taxes are not provided on translation adjustments as the earnings of the subsidiaries are considered to be permanently reinvested

.

Fair Value Measurements

The Company measures and discloses fair value in accordance with Financial Accounting Standards Board ("FASB") Accounting Standards CodificationASC 820 Fair Value Measurements and Disclosures ("ASC Topic 820"). ASC Topic 820Value”, which defines fair value, establishes a framework and gives guidance regarding the methods used for measuring fair value, and expands disclosures about fair value measurements. Fair value is an exit price, representing the amount that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. As such, fair value is a market-based measurement that should be determined based on assumptions that market participants would use in pricing an asset or liability. As a basis for considering such assumptions there exists a three-tier fair-value hierarchy, which prioritizes the inputs used in measuring fair value as follows:

Level 1 - unadjusted quoted prices are available in active markets for identical assets or liabilities that the Company has the ability to access as of the measurement date.


Level 2 – pricing inputs are other than quoted prices in active markets that are directly observable for the asset or liability or indirectly observable through corroboration with observable market data.
Level 3 – pricing inputs are unobservable for the non-financial asset or liability and only used when there is little, if any, market activity for the non-financial asset or liability at the measurement date. The inputs into the determination of fair value require significant management judgment or estimation. Fair value is determined using comparable market transactions and other valuation methodologies, adjusted as appropriate for liquidity, credit, market and/or other risk factors.

Level 2 - pricing inputs are other than quoted prices in active markets that are directly observable for the asset or liability or indirectly observable through corroboration with observable market data.

Level 3 - pricing inputs are unobservable for the non-financial asset or liability and only used when there is little, if any, market activity for the non-financial asset or liability at the measurement date. The inputs into the determination of fair value require significant management judgment or estimation. Fair value is determined using comparable market transactions and other valuation methodologies, adjusted as appropriate for liquidity, credit, market and/or other risk factors.

This hierarchy requires the Company to use observable market data, when available, and to minimize the use of unobservable inputs when determining fair value.

F-11


The fair value of cash and cash equivalents and short term bank deposits are based on its demand value, which is equal to its carrying value. The estimated fair values of notes payable, short-term and long-term debt which are based on borrowing rates that are available to the Company for loans with similar terms, collateral and maturity approximate the carrying values. Additionally, the carrying value of all other monetary assets (including long term receivables which bear interest) and liabilities (including the secured credit facilities) is estimated to be equal to their fair value due to the short-term nature of these instruments.

Derivative financial instruments are measured at fair value, on a recurring basis. The fair value

As of derivatives generally reflectsDecember 31, 2017, an option to purchase redeemable convertible preferred stock as embedded in the estimated amounts that the Group would receive or pay to terminate the contracts at the reporting dates, based on the prevailing currency prices and the relevant interest rates. Such measurement is classified within Level 2.

In addition to items that arePurchase Agreement (see also Note 14) was measured at fair value on a recurring basis there are also assets and liabilities that are measured at fair value on a nonrecurring basis. Assets and liabilities that are measured at fair value on a nonrecurring basis include certain long-lived assets including goodwill. As such, we have determined that each of these fair value measurements reside within Levelusing level 3 of the fair value hierarchy.
inputs.

Cash and Cash Equivalents

The Company investsinvested its excess cash in highly liquid short-term investments. The Company considersconsidered short-term investments that arewere purchased with an original maturity of three months or less to be cash equivalents. Cash and cash equivalents consisted of cash and money market accounts at December 31, 2014 and 2013.

Short-term Deposits

Short-term deposits are deposits with original maturities of more than three months but less than one year. Short-term deposits are presented at their costs including accrued interest.


Accounts Receivable

and Allowance for Doubtful Accounts

The majority of the Company'sCompany’s accounts receivable (other than LCA) arewere due from consumers, distributors (domestic and international), physicians and other entities in the medical field.field, divisions which are no longer operated by the Company. Accounts receivable arewere most often due within 30 to 90 days and are stated at amounts due from customers net of an allowance for doubtful accounts. Accounts outstanding longer than the contractual payment terms arewere considered past due. The Company determines its allowanceAllowance for doubtful accounts was determined by considering a number of factors, including the length of time trade accounts receivable are past due, the Company'sCompany’s previous loss history, the customer'scustomer’s current ability to pay its obligation to the Company and available information about their credit risk, and the condition of the general economy and the industry as a whole. The Company writeswrote off accounts receivable when they arewere considered uncollectible, and payments subsequently received on such receivables arewere credited to the allowance for doubtful accounts. The Company doesdid not recognize interest accruing on accounts receivable past due.

Patient Receivables and Allowance for Doubtful Accounts
The Company, through its subsidiary LCA-Vision (which is presented as a discontinued operations), provides financing to some As of its patients, including those who could not otherwise obtain third-party financing. The terms of the financing usually require the patient to pay an up-front fee which is intended to cover some or all of the variable costs, and then generally the remainder of the payments are automatically deducted from the patient's bank account over a period of 12 to 36 months. The Company has recorded an allowance for doubtful accounts as a best estimate of the amount of probable credit losses from the patient financing program. Each month, management reviews and adjusts the allowance based upon past experience with patient financing.
For patients that the Company internally finances, the Company charges interest at market rates. Finance and interest charges on patient receivables were $507 for the period ended December 31, 2014.
F-12


2016, the account receivable is included in the discontinued operation. As of December 31, 2017, there are no outstanding accounts receivable.

Inventories

Inventories arewere stated at the lower of cost or market. Cost is determined to be purchased cost for raw materials and the production cost (materials, labor and indirect manufacturing cost, including sub-contracted work components) for work-in-process and finished goods. For the Company'sCompany’s consumer and LHE products, cost iswas determined on the weighted-average method. For the pre-merged PhotoMedex'sPhotoMedex products, cost iswas determined on the first-in, first-out method. Throughout the laser manufacturing process, the related production costs are recorded within inventory. Work-in-process is immaterial, given the typically short manufacturing cycle, and therefore is disclosed in conjunction with raw materials.

The Company's equipment for the treatment of skin disorders (e.g. the XTRAC for psoriasis or vitiligo) will either (i) be placed in a physician's office and remain the property of the Company (at which date such equipment is transferred to property and equipment) or (ii) be sold to distributors or physicians directly. The cost to build a laser, whether for sale or for placement, is accumulated in inventory.

Reserves for slow moving and obsolete inventories arewere provided based on historical experience and product demand. Management evaluates the adequacy of these reserves periodically based on forecasted sales and market trend.

As of December 31, 2016, the inventory is included in the discontinued operation. As of December 31, 2017, there are no inventories.

Investment in Other Company

The investment in the other company is stated at cost, since the Company does not have the ability to exercise significant influence over operating and financial policies of those investees. The Company’s investments in the other company is reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount of an investment may not be recoverable, in accordance with ASC 320 “Investments – Debt and Equity Securities”. As of December 31, 2017, based on managements’ most recent analyses, impairment losses have been identified in the amount of $862 (see also Notes 5 and 13).

Property, Equipment and Depreciation

Property and equipment are recorded at cost, net of accumulated depreciation. Excimer lasers-in-service are depreciated on a straight-line basis over the estimated useful life of five years. For other property and equipment, depreciationDepreciation is calculated on a straight-line basis over the estimated useful lives of the assets, primarily three to seven years for computer hardware and software, furniture and fixtures, and machinery and equipment. Leasehold improvements are amortized over the lesser of the useful lives or lease terms. Expenditures for major renewals and betterments to property and equipment are capitalized, while expenditures for maintenance and repairs are charged as an expense as incurred. Upon retirement or disposition, the applicable property amounts are deducted from the accounts and any gain or loss is recorded in the consolidated statements of comprehensive (loss) income.loss. Useful lives are determined based upon an estimate of either physical or economic obsolescence or both.

Management evaluates the realizability

Realizability of property and equipment was based on estimates of undiscounted future cash flows over the remaining useful life of the asset. If the amount of such estimated undiscounted future cash flows iswas less than the net book value of the asset, the asset iswas written down to fair value. As of December 31, 2014, no such write-down was requiredvalue (see alsoImpairment of Long-Lived Assetsand Intangibles).

Patent Costs and Licensed Technologies

Costs incurred to obtain or defend patents and licensed technologies arewere capitalized and amortized over the shorter of the remaining estimated useful lives or eight to 12 years. Core and product technology was also recorded in connection with the reverse acquisition on December 13, 2011 and iswas being amortized on a straight-line basis over ten years for core technology and five years for product technology. (See technology (see also Note 6, 8).

Patent and Licensed Technologies).

Management evaluatesevaluated the recoverability of intangible assets based on estimates of undiscounted future cash flows over the remaining useful life of the asset. If the amount of such estimated undiscounted future cash flows is less than the net book value of the asset, the asset is written down to fair value. As ofDuring the year ended December 31, 2014, no such write-down was required. (See 2016, the Company recorded an impairment of patents and licensed technologies in the amount of $1,261 which is included in discontinued operation (see alsoImpairment of Long-Lived Assets and Intangibles).


Other Intangible Assets

Other intangible assets were recorded in connection with the reverse acquisition on December 13, 2011 and in connection with the acquisition of LCA.2011. The assets which were determined to have definite useful lives are beingwere amortized on a straight-line basis over ten years. Such assets primarily includeincluded customer relationships and trademarks. (See Note 79).,

Goodwill and Other Intangible Assets).

Management evaluates the recoverability of such other intangible assets based on estimates of undiscounted future cash flows over the remaining useful life of the asset. If the amount of such estimated undiscounted future cash flows is less than the net book value of the asset, the asset is written down to fair value. As of December 31, 2014 no such write-down was required. (See Impairment of Long-Lived Assets and Intangibles).
As of December 31, 2014, the indefinite life intangible is classified among the assets held for sale.
F-13


Accounting for the Impairment of Goodwill

The Company evaluates the carrying value of goodwill annually at the end of the calendar year and also between annual evaluations if events occur or circumstances change that would more likely than not reduce the fair value of the reporting unit to which goodwill was allocated to below its carrying amount. Such circumstances could include but are not limited to: (1) a significant adverse change in legal factors or in business climate, (2) unanticipated competition, or (3) an adverse action or assessment by a regulator. Goodwill impairment evaluation is performed subsequent to Impairment evaluation of long-lived assets and intangibles (see also Notes 6 and 7). Goodwill impairment testing involves a two-step process. Step 1 compares the fair value of the Group'sGroup’s reporting units to which goodwill was allocated to their carrying values. If the fair value of the reporting unit exceeds its carrying value, no further analysis is necessary. The reporting unit fair value is based upon consideration of various valuation methodologies, including guideline transaction multiples, multiples of current earnings, and projected future cash flows discounted at rates commensurate with the risk involved. If the carrying amount of the reporting unit exceeds its fair value, Step 2 must be completed to quantify the amount of impairment. Step 2 calculates the implied fair value of goodwill by deducting the fair value of all tangible and intangible assets, excluding goodwill, of the reporting unit, from the fair value of the reporting unit as determined in Step 1. The implied fair value of goodwill determined in this step is compared to the carrying value of goodwill. If the implied fair value of goodwill is less than the carrying value of goodwill, an impairment loss, equal to the difference, is recognized. See Note 2, regarding As part of the purchase price allocation for the 2011 reverse acquisition, the Company recorded goodwill in the amount of $24,005 and definite-lived intangibles in the amount of $12,000. Goodwill reflected the value or premium of the acquisition price in excess of the fair values assigned to specific tangible and intangible assets. Goodwill had an indefinite useful life and therefore was not amortized as an expense but was reviewed annually for impairment of goodwill whichits fair value to the Company. The fair value of Goodwill associated with the operating and reporting units was allocatedestimated using a combination of Income and Market Approach methodologies to LCA.

Accrued Enhancement Expense
valuation. The Company, through its subsidiary LCA-Vision (which is presented asIncome method of valuation explicitly recognizes the current value of future economic benefits developed by discounting future net cash flows to their present value at a discontinued operations), includes participation in its LasikPlus Advantage Plan® (acuity program)rate that reflects both the current return requirements of the market and the risks inherent in the base surgical price for substantially allmarket. The Market approach measures the value of its patients. Underan asset through the acuity program, if determined to be medically appropriate,analysis of recent sales or offerings of comparable property. Our business was organized into three operating and reporting units which were defined as Consumer, Physician Recurring, and Professional Equipment. Upon completion of our goodwill impairment analysis in connection with the transaction with ICTV Brands.

As of December 31, 2016, the Company provides post-surgical enhancements freerecorded an impairment of charge should the patient not achieveentire remaining balance of goodwill (allocated to consumer segment) in the desired visual correction during the initial procedure. Under this pricing structure, the Company accounts for the acuity program similar to a warranty obligation. Accordingly, the Company accrues the costs expected to be incurred to satisfy the obligation as a liability and costamount of revenue at the point of sale given its ability to estimate reasonably such costs$2,257 which is included in discontinued operation. Such determination was based on historical trends and the satisfaction of all other revenue recognition criteria.

This estimate is reviewed throughout the year with consideration to factors such as procedure cost and historical procedure volume when determining the appropriateness of the recorded balance.
market approach.

Accrued Warranty Costs

The Company offersoffered a standard warranty on product sales of its previous skin care business generally for a one to two-year period. In the case of domestic sales of XTRAC lasers, however, the Company has offered longer warranty periods, ranging from three to four years, in order to meet competition or meet customer demands. The Company providesprovided for the expected cost of estimated future warranty claims on the date the product is sold. Total accrued warranty iswas included in other accrued liabilities on the balance sheet. The activity in the warranty accrual during the years ended December 31, 20142017 and 20132016 is summarized as follows:

  December 31, 
  2014  2013 
Accrual at beginning of year $1,151  $1,440 
Additions charged to warranty expense  808   1,206 
Expiring warranties  (341)  (410)
Claims satisfied  (857)  (1,085)
Total  761   1,151 
Less: current portion  (665)  (1,094)
Long term accrued warranty $96  $57 

  December 31, 
  2017  2016 
Accrual at beginning of year $241  $330 
Additions charged to warranty expense     56 
Expiring warranties     (145)
Sale of consumer segment (*)  (241)    

Total (**)

     241 
Less: current portion     (241)
Long term accrued warranty $  $ 

(*) The buyer of the remaining consumer products business assumed the warranty obligations.

(**) Included in liabilities related to assets held for sale.

For extended warranty on the consumer products, see alsoRevenue Recognition below. below.

F-14


Insurance Reserves

Revenue Recognition

The Company through its subsidiary LCA-Vision (which is presented as a discontinued operations), maintains a captive insurance company to provide professional liability insurance coverage for claims brought against the Company and its optometrists. In addition, the captive insurance company's charter allows it to provide professional liability insurance for the Company's ophthalmologists, none of whom are currently insured by the captive. The Company uses the captive insurance company for both primary insurance and excess liability coverage. A number of claims are now pending with the captive insurance company. Since the captive insurance company is wholly-owned enterprise, it is included in the Company's consolidated financial statements. As of December 31, 2014, the insurance reserves were $6,044, which represented an actuarially determined estimate of future costs associated with claims filed as well as claims incurred but not yet reported. The actuaries determine loss reserves by comparing the Company's historical claim experience to comparable insurance industry experience.

Revenue Recognition
The Company recognizesrecognized revenues from the product sales when the following four criteria have been met: (i) the product has been delivered and the Company has no significant remaining obligations; (ii) persuasive evidence of an arrangement exists; (iii) the price to the buyer is fixed or determinable; and (iv) collection is reasonably assured. Revenues from product sales are recorded net of provisions for estimated chargebacks, rebates, expected returns and cash discounts.

The Company shipsshipped most of its products FOB shipping point, although from time to time certain customers, for example governmental customers, will be granted FOB destination terms. Among the factors the Company takes into account when determining the proper time at which to recognize revenue are (i) when title to the goods transfers and (ii) when the risk of loss transfers. Shipments to distributors or physicians that do not fully satisfy the collection criteria are recognized when invoiced amounts are fully paid or fully assured and included in deferred revenues until that time.

For revenue arrangements with multiple deliverables within a single, contractually binding arrangements (usually sales of products with separately priced extended warranty), each element of the contract is accounted for as a separate unit of accounting when it provides the customer value on a stand-alone basis and there is objective evidence of the fair value of the related unit.

With respect to sales arrangements under which the buyer hashad a right to return the related product, revenue iswas recognized only if all the following conditions are met: the price iswas fixed or determinable at the date of sale; the buyer has paid, or iswas obligated to pay and the obligation iswas not contingent on resale of the product; the buyer'sbuyer’s obligation would not be changed in the event of theft or physical destruction or damage of the product; the buyer hashad economic substance; the Company doesdid not have significant obligations for future performance to directly bring about resale of the product by the buyer; and the amount of future returns cancould be reasonably estimated.

The Company providesprovided a provision for product returns based on the experience with historical sales returns, in accordance with ASC Topic 605-15 with respect to sales of product when a right of return exists. existed. Reported revenues are shown net of the returns provision. Such allowance for sales returns iswere included inOther Accrued Liabilities. (See (see also Note 9)11).

Deferred revenue includesincluded amounts received with respect to extended warranty maintenance, repairs and other billable services and amounts not yet recognized as revenues. Revenues with respect to such activities arewere deferred and recognized on a straight-line basis over the duration of the warranty period, the service period or when service iswas provided, as applicable to each service.

The Company has two distribution channels for its phototherapy treatment equipment. The Company either (i) sells its lasers through a distributor or directly to a physician or (ii) places its lasers in a physician's office (at no charge to the physician) and generally charges the physician a fee for an agreed upon number of treatments. In some cases, the Company and the customer stipulate to a quarterly or other periodic target of procedures to be performed, and accordingly revenue is recognized ratably over the period.
F-15


When the Company places a laser in a physician's office, it generally recognizes service revenue based on the number of patient treatments performed, or purchased under a periodic commitment, by the physician. Amounts collected with respect to treatments to be performed through laser-access codes that are sold to physicians free of a periodic commitment, but not yet used, are All such deferred and recognized as a liability until the physician performs the treatment. Unused treatments remain an obligation of the Company because the treatments can only be performed on Company-owned equipment. Once the treatments are performed, this obligation has been satisfied.
The Company defers substantially all revenue from sales of treatment codes ordered by and performed to its customers within the last two weeks of the period in determining the amount of treatments performed by its physician-customers. Management believes this approach closely approximates the actual amount of unused treatments that existed at the end of a period.
revenues were derecognized.

Shipping and Handling Costs

Shipping and handling fees billed to customers arewere reflected as revenues while the related shipping and handling costs arewere included in selling and marketing expense. To date, shippingShipping and handling costs have not been material.

Product Development Costs
Costs of research, new product development and product redesign are charged to expense as incurred in engineering and product development.

Advertising Costs

Advertising costs arewere charged to expenses as incurred.

Advertising expenses amountedcosts were included in the loss on discontinued operations (see Note 2 Discontinued Operation).

Concentrations of credit risk

Financial instruments which subject the Company to approximately $62,197, $71,992concentrations of credit risk consist primarily of cash and $60,651 for the years ended December 31, 2014, 2013 and 2012, respectively.

Derivatives
cash equivalents. The carrying amounts of these instruments approximate fair value due to their short-term nature. The Company applies the provisions of Accounting Standards Codification ("ASC") Topic 815, Derivativesdeposits cash and Hedging. In accordance with ASC Topic 815, all the derivativecash equivalents and short-term deposits in major financial instruments are recognized as either financial assets or financial liabilities on the balance sheet at fair value. The accounting for changesinstitutions in the fair valueUS, UK, and in Israel. The Company performs periodic evaluations of a derivative financial instrument depends on whether it has been designated and qualifies as partthe relative credit standing of a hedging relationship and further, onthese institutions. The Company is of the typeopinion that the credit risk in respect of hedging relationship. For derivative financial instruments that are designated and qualify as hedging instruments, a company must designate the hedging instrument, based upon the exposure being hedged, as a fair value hedge, cash flow hedge or a hedge of a net investment in a foreign operation.
From time to timethese balances is immaterial. In addition, the Company carries out transactions involving foreign exchange derivative financial instruments (mainly forward exchange contracts) which are expected to be paidperformed with respect to forecasted expensesits previous skin business an ongoing credit evaluation and established an allowance for doubtful accounts based upon factors surrounding the credit risk of customers (see alsoAccounts Receivable above).

Concentrations of credit risk

Most of the Israeli subsidiary (Radiancy) denominatedCompany’s sales were generated in Israeli local currency (NIS) which is different than its functional currency.

Such derivativesNorth America and Asia Pacific, to a large number of customers. Management periodically evaluated the collectability of the trade receivables to determine the amounts that were doubtful of collection and determine a proper allowance for doubtful accounts. Accordingly, the Company’s trade receivables did not designated as hedging instruments, and accordingly they were recognized in the balance sheet at their fair value, with changes in the fair value carried to the Statementrepresent a substantial concentration of Comprehensive (Loss) Income and included in interest and other financing income (expenses), net.
At December 31, 2014, the balance of such derivative instruments amounted to approximately $726 in liabilities and approximately $689 were recognized as financing loss in the Statement of Comprehensive (Loss) Income during the year ended that date. At December 31, 2013, the balance of such derivative instruments amounted to approximately $255 in assets and approximately $699 were recognized as financing income in the Statement of Comprehensive (Loss) Income during the year ended that date.
The notional amounts of foreign currency derivatives as of December 31, 2014 consist of forward transactions for the exchange of $11,000 into NIS and $6,725 as of December 31, 2013.
F-16

credit risk.

Income Taxes

The Company accounts for income taxes using the asset and liability method. Under this method, deferred tax assets and liabilities are determined based on differences between the financial reporting and tax basis of assets and liabilities and are measured using enacted tax rates and laws that are expected to be in effect when the differences reverse. Any resulting net deferred tax assets are evaluated for recoverability and, accordingly, a valuation allowance is provided when it is more likely than not that all or some portion of the deferred tax asset will not be realized.realized.


The Company or its subsidiaries may incur an additional tax liabilityliabilities in the event of an intercompany dividend distribution or a deemed dividend distribution under the U.S. income tax law and regulations. Prior to 2014, it was the Company'sCompany’s policy not to cause a distribution of dividends which would generate an additional tax liability to the Company. During the years ended December 31, 2014 and 2015, the CompanyCompany’s affiliates borrowed funds from itsthe subsidiary in Israel. These borrowings resulted in a large deemed distribution taxable in the U.S. Furthermore, Managementmanagement can no longer represent that the earnings of its non U.S. subsidiaries will remain permanently invested outside the U.S. Therefore, beginning in 2014, the Company has provided deferred taxes on the undistributed earnings of its non U.S. subsidiaries. Taxes, which wouldmay apply in the event of a disposal of investments in subsidiaries, have not been taken into accountincluded in computing the deferred taxes, as the Company anticipates it is the Company's policy to hold these investments, not to dispose of them.

would liquidate those subsidiaries that can be closed on a tax-free basis.

The Company accounts for uncertain tax positions in accordance with an amendment to ASC Topic 740-10, Income Taxes (Accounting for Uncertainty in Income Taxes), Taxes”which clarified the accounting for uncertainty in tax positions. This amendment provides that the tax effects from an uncertain tax position can be recognized in the financial statements only if the position is "more-likely-than-not"“more-likely-than-not” to be sustained were it to be challenged by a taxing authority. The assessment of the tax position is based solely on the technical merits of the position, without regard the likelihood that the tax position may be challenged. If an uncertain tax position meets the "more-likely-than-not"“more-likely-than-not” threshold, the largest amount of tax benefit that is more than 50% likely to be recognized upon ultimate settlement with the taxing authority is recorded.

In

During the yearyears ended December 31, 2014,2017 and 2016, the Company determined that the liability for unrecognized tax benefits could suitably be extinguished by application of net operating loss carryforwards and carrybacks, with any residual impact arising as a liability in 20142017 and 2016 that has been duly provided for.

Concentration of credit risks
Financial instruments which subject the Company to concentrations of credit risk consist primarily of cash and cash equivalents, derivative (assets), accounts receivable and short-term bank deposits. The carrying amounts of these instruments approximate fair value due to their short-term nature. The Company deposits cash and cash equivalents and short term deposits in major financial institutions in the US, UK, Brazil and in Israel. The Company performs periodic evaluations of the relative credit standing of these institutions. The Company is of the opinion that the credit risk in respect of these balances is immaterial. In addition, the Company performs an ongoing credit evaluation and establishes an allowance for doubtful accounts based upon factors surrounding the credit risk of customers (see also

Accounts receivableContingencies above).

Most of the Company's sales are generated in North America and Asia Pacific, to a large number of customers. Management periodically evaluates the collectability of the trade receivables to determine the amounts that are doubtful of collection and determine a proper allowance for doubtful accounts. Accordingly, the Company's trade receivables do not represent a substantial concentration of credit risk.
Contingencies

The Company and its subsidiaries are involved in certain legal proceedings that arise from time to time in the ordinary course of its business. We account for business contingent liabilities in accordance with ASC 450 “Contingencies”. Except for income tax contingencies, the Company records accruals for contingencies to the extent that the management concludes that the occurrence is probable and that the related amounts of the loss can be reasonably estimated. A provision is recorded when it is both probable and when a liability has been incurred and the related amounts of the loss can be reasonably estimated. Legal expenses associated costs incurred in connection with the contingencycontingencies are expensed as incurred.

F-17

Earnings (Loss) Per Share
The Company computes earnings (net loss) per share in accordance with ASC Topic. 260, Earnings per share. Basic earnings (loss) per share

With respect to legal matters, provisions are computed by dividing net income by the weighted-average number of common shares outstanding during the period, net of the weighted average number of treasury shares. Diluted earnings (loss) per common share are computed similarreviewed and adjusted to basic earnings per share, except that the denominator is increased to include the number of additional potential common shares that would have been outstanding if the potential common shares had been issued and if the additional common shares were dilutive. Potential common shares are excluded from the computation for a period in which a net loss is reported or if their effect is anti-dilutive. The Company's potential common shares consist of stock options, warrants and restricted stock awards issued under the Company's stock incentive plans and their potential dilutive effect is considered using the treasury method.

Basic and diluted earnings per common share were calculated using the following weighted average shares outstanding for the years ended December 31, 2014, 2013 and 2012:
  December 31,
  2014 2013 2012
Weighted average number of common and common equivalent shares outstanding:      
Basic number of common shares outstanding 18,940,355 20,454,970 20,355,520
Dilutive effect of stock options and warrants - 202,270 408,834
Diluted number of common and common stock equivalent shares outstanding 18,940,355 20,657,240 20,764,354
Diluted earnings (loss) per share for each of the years ended December 31, 2014, 2013 and 2012 excludereflect the impact of common stock options, warrantsnegotiations, estimated settlements, legal rulings, advice of legal counsel and unvested restricted stock totaling 2,540,733, 2,172,745other information and 1,920,442 shares, respectively,events pertaining to a particular matter. Other than the matters discussed in Note 13, as of December 31, 2017, the Company is not a party to any other litigation that it believes would have a material adverse effect on the Company’s business, financial position, results of their inclusion would be anti-dilutive.
operations or cash flows.

Impairment of Long-Lived Assets and Intangibles

Long-lived assets, such as property and equipment, and definite-lived intangibles subject to amortization, are reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset (or group of assets) may not be recoverable. Impairment test is applied at the lowest level where there are identifiable independent cash flows, which may involve a group of assets.

Recoverability of assets to be held and used (or group of assets) is measured by a comparison of the carrying amount of an asset to the fair value ofundiscounted cash flows expected to be generated by the asset. If the carrying amount of an asset exceeds the fair value,is determined to be impaired, an impairment charge is recognized in the amount by which the carrying amount of the asset exceeds the fair value of the asset. As of December 31, 2014, (other than the measurement of LCA net assets based on it estimated fair value less cost to sell- see Note 2) no such impairment exists. Assets to be disposed of are separately presented in the balance sheet and reported at the lower of the carrying amount or fair value less costs to sell and are no longer depreciated. The assets and liabilities of a disposed group classified as discontinued operations are presented separately in the appropriate asset and liability sections of the balance sheet.


Indefinite-life intangible assets are tested for impairment, on an annual basis or more often, when triggering events indicate that it is more likely than not that the asset is impaired, by comparing the fair value of the asset with its carrying amount. If the carrying amount of the intangible asset exceeds its fair value, an impairment loss is recognized in the amount of that excess. Subsequent reversal of a previously recognized impairment loss is prohibited.

Pursuant to ASC 360 the Company tested the long-lived assets and determined that changes in circumstances indicated that its carrying value may not be recoverable. The carrying amount of the assets is considered recoverable if it exceeds the sum of undiscounted cash flows expected from the use or eventual disposition of the asset. Upon completion of our goodwill impairment analysis in connection with the pending transaction with ICTV Brands, as of December 31, 2016, the Company recorded an impairment of the entire remaining balance of Consumer segment goodwill in the amount of $2,257. The Company recorded an impairment of the Consumer segment intangibles for its entire remaining Licensed Technology balance in the amount of $1,261. These impairment charges are included in discontinued operations.

Loss per Share

The Company computes net loss per share in accordance with ASC 260,“Earnings per share”. Basic loss per share are computed by dividing net loss by the weighted-average number of common shares outstanding during the period, net of the weighted average number of treasury shares (if any). Securities that may participate in dividends with the Common Stock (such as the convertible Preferred Stock Series A and Series B) are considered in the computation of basic income per share using the two-class method. However, in periods of net loss, participating securities are included only if the holders of such securities have a contractual obligation to share the losses of the Company. Accordingly, the outstanding Series A preferred shares were included in the computation, while the Series B preferred shares were not.

Diluted loss per common share is computed similar to basic earnings per share, except that the denominator is increased to include the number of additional potential common shares that would have been outstanding if the potential common shares had been issued and if the additional common shares were dilutive. Potential common shares are excluded from the computation for a period in which a net loss is reported or if their effect is anti-dilutive. The Company’s potential common shares consist of stock options, stock warrants and restricted stock awards issued under the Company’s stock incentive plans and their potential dilutive effect is considered using the treasury method and of convertible Preferred Stock Series A and Series B which their potential dilutive effect is considered using the “if-converted method”.

The net loss from continuing operations and the weighted average number of shares used in computing basic and diluted net loss per share from continuing operations for the years ended December 31, 2017 and 2016, is as follows: (in thousands except share and per share amounts)

  Year ended December 31, 
  2017  2016 
       
Numerator:        
Net loss attributable to common stockholders $18,807  $13,264 

Net loss from discontinued operations attributable to common stockholders

  (2,459)  (13,264)
Accretion of dividend for the period (*)  3    
Participation of stockholders of series A preferred stock in the net loss from continuing operations  (1,318)   
         
Net loss from continuing operations attributable to common stockholders $15,033  $ 
         
Denominator:        
Shares of common stock used in computing basic and diluted net loss per share  5,073,751   4,171,549 
         

Net loss per share of Ordinary Share from continuing operations, basic and diluted

 $2.96  $ 

(*)The net loss used for the computation of basic and diluted net loss per share for the year ended December 31, 2017, includes the dividend requirement of 8% per share per annum for the Series B preferred stock, compounded annually which shall be distributed to stockholders in case of distributable assets determined in the Company’s certificate of designation (the “Certificate of Designation”) under the liquidation preference right (see also Note 14).


For the year ended December 31, 2017, diluted loss per share excludes the impact of stock options, stock warrants, series Preferred A Stock, series Preferred B Stock, common stock to be issued upon exercise of asset contribution financial instruments and common stock to be issued upon written call option totaling 43,053,913 shares, as the effect of their inclusion would be anti-dilutive. For the year ended December 31, 2016, diluted loss per share excludes the impact of stock options totaling 1,000 shares.

Convertible Redeemable Series B Preferred Stock

The Company classifies its Convertible Redeemable Series B Preferred Stock outside of Stockholders’ deficit because certain features of the Company’s Certificate of Designation could require redemption of some or all classes of Convertible Redeemable Series B Preferred Stock upon events not solely within the control of the Company (see also Note 14).

Option to purchase Convertible Redeemable Series B Preferred Stock:

The Company has classified the option to purchase additional shares of its Convertible Redeemable Series B Preferred Stock as a liability in accordance with ASC 480, “Distinguishing Liabilities from Equity” as the underlying Series B Preferred Shares are subject to redemption feature. The Company measures the option at fair value by using the Black Scholes Pricing Model in each reporting period until they are exercised or expired, with changes in the fair values being recognized in the Company’s statement of comprehensive loss (see also Note 14).

Stock-Based Compensation

The Company accounts for stock-based compensation in accordance with ASC Topic 718, Compensation Stock Compensation.Compensation. Under”, (“ASC 718”), which requires companies to estimate the fair value recognition provision, of this statement, share-basedshare-equity based compensation cost is measured at payment awards on the date of grant date based on the fair using an option pricing model. The value of the portion of the award that is ultimately expected to vest and is recognized as operating an expense over the applicable vesting period of requisite service periods in the stock award using Company’s consolidated statement of comprehensive loss.

The Company recognizes compensation expense for the value of its awards granted based on the graded vesting method.

Treasury Stock and Repurchasemethod over the requisite or derived service period of Common Stock
Shares held by the Company are presented as a reduction of equity, at their cost to the Company as treasury stock, until such shares are retired and removed from the accounts.
F-18


Adoption of New Accounting Standards
Effective January 1, 2014, the Company adopted Accounting Standard Update 2013-11, Income Taxes (Topic 740): Presentation of an Unrecognized Tax Benefit When a Net Operating Loss Carryforward, a Similar Tax Loss, or a Tax Credit Carryforward Exists (a consensuseach of the awards, net of estimated forfeitures. ASC 718 requires forfeitures to be estimated at the time of grant and revised, if necessary, in subsequent periods if actual forfeitures differ from those estimates.

The Company estimates the fair value of stock options granted using the Black-Scholes-Merton option-pricing model which requires a number of assumptions, of which the most significant are the expected stock price volatility and the expected option term. Expected volatility was calculated based upon historical daily stock price observations of its common stock. The expected option term represents the period that the Company’s stock options are expected to be outstanding and is determined based on the simplified method until sufficient historical exercise data will support using expected life assumptions. The risk-free interest rate is based on the yield from U.S. treasury bonds with an equivalent term. The Company has historically not paid dividends and has no foreseeable plans to pay dividends. 

Recently Issued Accounting Standards

Recent Accounting Pronouncements adopted

On March 30, 2016, the FASB Emerging Issues Task Force) ("issued ASU 2013-11").

2016-09, “Compensation-Stock Compensation”, which effects all entities that issue share-based payment awards to their employees. The amendments in ASU 2013-11 state thatthis update cover such areas as the recognition of excess tax benefits and deficiencies, the classification of those excess tax benefits on the statement of cash flows, an unrecognized tax benefit, or a portion ofaccounting policy election for forfeitures, the amount an unrecognized tax benefit, should be presented in the financial statements as a reductionemployer can withhold to a deferred tax asset for a net operating loss carryforward, a similar tax loss, or a tax credit carryforward, except as follows: To the extent a net operating loss carryforward, a similar tax loss, or a tax credit carryforward is not available at the reporting date under the tax law of the applicable jurisdiction to settle any additionalcover income taxes that would result from the disallowance of a tax position or the tax law of the applicable jurisdiction does not require the entity to use,and still qualify for equity classification and the entity does not intend to use,classification of those taxes paid on the deferred tax asset for such purpose, the unrecognized tax benefit should be presented in the financial statements as a liability and should not be presented netstatement of deferred tax assets.
ASU 2013-11 applies to all entities that have unrecognized tax benefits when a net operating loss carryforward, a similar tax loss, or a tax credit carryforward exists at the reporting date. For public companies the amendments in this ASU becamecash flows. This update is effective for fiscal years,annual and interim periods within those years, beginning after December 15, 2013.2016. This guidance can be applied either prospectively, retrospectively or using a modified retrospective transition method. The amendments were appliedCompany adopted the new guidance prospectively to all unrecognized tax benefits that existed at the effective date.
The adoption of the standardJanuary 1, 2017. This new guidance did not have a material impact on the Company'sCompany’s consolidated results of operations and financial condition.statements.


Effective January 1,

Recent Accounting Pronouncements not adopted yet

In May 2014, the Company adoptedFinancial Accounting Standards Board (“FASB”) issued Accounting Standards Update 2013-5(“ASU”) No. 2014-09, Revenue from Contracts with Customers (Topic 606) (ASU 2014-09), Foreign Currency Matterswhich amends the existing accounting standards for revenue recognition. In August 2015, FASB issued ASU No. 2015-14, Revenue from Contracts with Customers (Topic 830) Parent's Accounting for the Cumulative Translation Adjustment upon Derecognition of Certain Subsidiaries or Groups of Assets within a Foreign Entity or of an Investment in a Foreign Entity ("ASU 2013-5").

ASU 2013-5 clarifies that, when a reporting entity (parent) ceases to have a controlling financial interest in a subsidiary or group of assets that is a business (other than a sale of in-substance real estate or conveyance of oil and gas mineral rights) within a foreign entity, the parent is required to apply the guidance in Subtopic 830-30 to release any related cumulative translation adjustment into net income. Accordingly, the cumulative translation adjustment should be released into net income only if the sale or transfer results in the complete or substantially complete liquidation606): Deferral of the foreign entity inEffective Date, which the subsidiary or group of assets had resided. ASU 2013-5 also clarifies that if the business combination achieved in stages relates to a previously held equity method investment (step-acquisition) that is a foreign entity, the amount of accumulated other comprehensive income that is reclassified and included in the calculation of gain or loss shall include any foreign currency translation adjustment related to that previously held investment.
For public companies, the amendments in this Update became effective prospectively for fiscal years (and interim reporting periods within those years) beginning after December 15, 2013. In accordance with the transition requirements, the amendments were applied prospectively to derecognition events occurring afterdelays the effective date. Prior periods are not required be adjusted.
The adoptiondate of ASU 2014-09 by one year. FASB also agreed to allow entities to choose to adopt the standard as of the original effective date. The new revenue recognition standard did not have a material impact on the Company's consolidated results of operations and financial condition.
Recently Issued Accounting Standards
In April 2014, the FASB issued Accounting Standard Update 2014-08, Presentation of Financial Statements (Topic 205) and Property, Plant, and Equipment (Topic 360): Reporting Discontinued Operations and Disclosures of Disposals of Components of an Entity ("ASU 2014-08").
The amendments in ASU 2014-08 change the criteria for reporting discontinued operations while enhancing disclosures in this area. Under the new guidance, only disposals representing a strategic shift in operations shouldwill be presented as discontinued operations. Those strategic shifts should have a major effect on the organization's operations and financial results. In addition, the new guidance requires expanded disclosures about discontinued operations that will provide financial statement users with more information about the assets, liabilities, income, and expenses of discontinued operations.
F-19


The amendments in ASU 2014-08 are effective in the first quarter of 20152018, with the option to adopt it in the first quarter of 2017. The Company currently anticipates adopting the new standard effective January 1, 2018. The new standard also permits two methods of adoption: retrospectively to each prior reporting period presented (full retrospective method), or retrospectively with the cumulative effect of initially applying the guidance recognized at the date of initial application (the modified retrospective method). In April 2016, FASB issued ASU 2016-10, Revenue from Contracts with Customers (Topic 606): Identifying Performance Obligations and Licensing. ASU 2016-10 covers two specific topics: performance obligations and licensing. This amendment includes guidance on immaterial promised goods or services, shipping or handling activities, separately identifiable performance obligations, functional or symbolic intellectual property licenses, sales-based and usage-based royalties, license restrictions (time, use, geographical) and licensing renewals. In addition, in May 2016, FASB issued ASU No. 2016-12, Revenue from Contracts with Customers (Topic 606): Narrow-Scope Improvements and Practical Expedients, which is intended to not change the core principle of the guidance in Topic 606, but rather affect only the narrow aspects of Topic 606 by reducing the potential for public companiesdiversity in practice at initial application and by reducing the cost and complexity of applying Topic 606 both at transition and on an ongoing basis. The Company is not expecting that the adoption of this standard will have a material impact on its financial statements and related disclosures. 

In February 2016, the FASB issued ASU 2016-02, “Leases”. This guidance will require that lease arrangements longer than 12 months result in an entity recognizing an asset and liability equal to the present value of the lease payments in the statement of financial position. This guidance is effective for annual periods beginning after December 15, 2018, and interim periods therein. This standard requires a modified retrospective transition approach for all leases existing at, or entered into after, the date of initial application, with calendar year ends.an option to use certain transition relief. Early adoption is permitted.

The Company is currently evaluating the impact that the adoption of ASU 2014-082016-02 will have on its financial statements and related disclosures.

In November 2016, the FASB issued ASU 2016-18, Statement of Cash Flows (Topic 230): “Restricted Cash” (ASU 2016-18), which requires companies to include amounts generally described as restricted cash and restricted cash equivalents in cash and cash equivalents when reconciling beginning-of-period and end-of-period total amounts shown on the statement of cash flows. The amendments in this update are effective for public business entities for fiscal years beginning after December 15, 2017, and interim periods within those fiscal years. Early adoption is permitted, including adoption in an interim period, however, the Company has not elected to early adopt ASU 2016-18. This new guidance is not expected to have a material impact on the Company'sCompany’s consolidated results of operations and financial condition.

statements. 

In May 2014, TheJanuary 2017, the FASB issued Accounting Standard Update 2014-09, Revenue from Contracts with CustomersASU 2017-01 Business Combinations (Topic 606) ("805): “Clarifying the Definition of a Business”. ASU 2014-09").

ASU 2014-09 outlines2017-01 provides amendments to clarify the definition of a single comprehensive modelbusiness and affect all companies and other reporting organizations that must determine whether they have acquired or sold a business. The amendments are intended to use in accountinghelp companies and other organizations evaluate whether transactions should be accounted for revenue arising from contracts with customers and supersedes most current revenue recognitionas acquisitions (or disposals) of assets or businesses. The guidance including industry-specific guidance. ASU 2014-09 also requires entities to disclose sufficient information, both quantitative and qualitative, to enable users of financial statements to understand the nature, amount, timing, and uncertainty of revenue and cash flows arising from contracts with customers.
An entity should apply the amendments in this ASU using one of the following two methods: 1. Retrospectively to each prior reporting period presented with a possibility to elect certain practical expedients, or, 2. Retrospectively with the cumulative effect of initially applying ASU 2014-09 recognized at the date of initial application. If an entity elects the latter transition method, it also should provide certain additional disclosures.
For a public entity, the amendments in ASU 2014-09 areis effective for annual reporting periodspublic business entities for fiscal years beginning after December 15, 2016,2017, and interim periods within those fiscal years and should be applied prospectively as of the beginning of the period of adoption. Early adoption is permitted under certain circumstances. The Company is currently evaluating the potential effect of the guidance on its consolidated financial statements.

In May 2017, the FASB issued ASU 2017-09 “Compensation-Stock Compensation (Topic 718): Scope of Modification Accounting”, which includes guidance on changes to terms and conditions of share-based payment awards. The amendment provides guidance about which changes to terms or conditions of a share-based payment award require an entity to apply modification accounting. The guidance will be effective for the fiscal year beginning on January 1, 2018, including interim periods within that reporting period (the first quarter of fiscal year 2017 for the Company). Early application(early adoption is not permitted.permitted). The Company is incurrently evaluating the processpotential effect of assessing the impact, if any, of ASU 2014-09guidance on its consolidated financial statements.


In August 2014, the FASB issued Accounting Standards Update 2014-15,

Presentation of Financial Statements—Going Concern (Subtopic 205-40): Disclosure of Uncertainties about an Entity's Ability to Continue as a Going Concern Note 4("ASU 2014-15"). ASU 2014-15 provide guidance on management's responsibility in evaluating whether there are conditions or events, considered in the aggregate, that raise substantial doubt about the entity's ability to continue as a going concern within one year after the date that the financial statements are issued (or within one year after the date that the financial statements are available to be issued when applicable). ASU 2014-15 also provide guidance related to the required disclosures as a result of management evaluation.

The amendments in ASU 2014-15 are effective

Discontinued Operations Assets Held for the annual period ending after December 15, 2016, and for annual periods and interim periods thereafter. Early applicationSale:

A disposal group is permitted.

Note 2
Discontinued Operations:
LCA is a provider of fixed-site laser vision corrections services at its LasikPlus® vision centers. The vision centers provide the staff, facilities, equipment and support services for performing laser vision correction that employs advanced laser technologies to help correct nearsightedness, farsightedness and astigmatism. The vision centers are supported by independent ophthalmologists and credentialed optometrists, as well as other healthcare professionals. Substantially all of LCA's revenues are derived from the delivery of laser vision correction procedures performed in the vision centers. After preliminary investigations and discussions, the Board of Directors of the Company, with the aid of its investment banker, had reached a formal decision during December 2014 to enter into, substantive, confidential discussions with potential third-party buyers and began to develop plans for implementing a disposal of the assets and operations of the business. The Company accordingly classified this former segmentreported as held for sale in accordancewhen management has approved or received approval to sell and discontinued operations with ASC Topic 360. On February 2, 2015,is committed to a formal plan, the Company closed ondisposal group is available for immediate sale, transactionthe business is being actively marketed, the sale is anticipated to occur during the next 12 months and certain other specified criteria are met. A disposal group classified as held for sale is recorded at the lower of 100%its carrying amount or estimated fair value less cost to sell. If the carrying value of the shares of LCA for $40 million in cash. Excludingbusiness exceeds its estimated working capital adjustments and direct expenses (professional fees to third parties), PhotoMedex realized net proceeds of approximately $36.5 million which amount is considered as the fair value less cost to sell, of LCA as of December 31, 2014. Thea loss is recognized. However, when disposal group meets the held for sale was effective January 31, 2014. No income tax benefit was recognized bycriteria, the Company fromfirst evaluates whether the loss on the sale of discontinued operations.
F-20

The accompanying consolidated financial statements reflect the operating results and balance sheet itemscarrying amounts of the discontinued operations separately from continuing operations. The Company recognized an estimated loss of $44,598 on the sale of the discontinued operationsassets not covered by ASC 360-10 included in the year ended December 31, 2014, which included a decrease in the implied fair value of goodwill, related to LCA, of $43,091. The remaining loss of $1,507 represents the difference between the adjusted net purchase price and the carrying value of the disposal group. The impairment amount is categorizedgroup (such as level 3 measurements.
Revenues from LCA, reported as discontinued operations, for the year ended December 31, 2014 was $47,198. Loss from LCA, reported as discontinued operations, for the year ended December 31, 2014 was $15,155, which includes tax expense of $5,496 and interest expense of $2,065 related to the portion of the credit facility that wasgoodwill) are required to be paid as a result ofadjusted in accordance with other applicable GAAP before measuring the sale.
The following is a summary of assetsdisposal group at fair value less cost to sell.

Assets and liabilities related to a disposal group classified as held for sale are segregated in the consolidated balance sheet in the period in which the disposal group is classified as held for sale.

Only disposal of a component of an entity or a group of components of an entity that represents a strategic shift that has or will have a major effect on an entity’s operations and financial results shall be reported as discontinued operations. The revised guidance did not change the criteria required to qualify for held for sale presentation.

In connection with the sale of the Consumer Division to ICTV Brands, Inc., announced on October 4, 2016 and subsequently completed on January 23, 2017, the assets related to this transaction were included as of December 31, 2014:

  December 31, 2014 
Assets:  
Cash and cash equivalents $4,514 
Accounts receivable  2,759 
Inventories  119 
Deferred tax assets  1,930 
Other current assets  2,492 
Property & Equipment, net  14,519 
Goodwill, net  6,491 
Other intangible assets, net  38,331 
Other assets  1,207 
Assets held for sale  72,362 
Less: Impairment  (1,507)
Assets held for sale, net $70,855 
     
Liabilities:    
Accounts payable $5,518 
Other accrued liabilities  5,933 
Deferred revenues  97 
Long term debt:  1,080 
Other liabilities  6,870 
Deferred tax liability  14,999 
Liabilities held for sale  34,497 
     
Total net assets of discontinued operations $36,358 
2016 as part of Assets Held for Sale, as follows:

Inventory $7,336 
Property and equipment  911 
Other assets  115 
Assets held for sale as of December 31, 2016 $8,362 

Note 3

Acquisition:
Acquisition5

Acquisitions:

On March 31, 2017, the Company and its newly-formed subsidiary FC Global Realty Operating Partnership, LLC, a Delaware limited liability company (“Acquiror”) entered into an Interest Contribution Agreement (the “Contribution Agreement”) with First Capital Real Estate Operating Partnership, L.P., a Delaware limited partnership (“Contributor”), and First Capital Real Estate Trust Incorporated, a Maryland corporation, (the “Contributor Parent” and, together with Contributor, the “Contributor Parties”), under which the Contributor will contribute mostly certain real estate assets (the “Contributed Properties”) to the Company’s subsidiary. In exchange, the Contributor will receive shares of LCA-Vision Inc.:

the Company’s Common Stock and/or newly designated Series A Convertible Preferred Stock.

The first installment of contributed assets (the “First Contribution”) closed on May 17, 2017 (the “Initial Closing”).

First Contribution

In the Initial Closing, the Contributor transferred certain assets comprising the Contributed Properties to the Company. On May 12, 2014, PhotoMedex Inc.,the Initial Closing date, the Contributor transferred to the Acquiror four vacant land sites set for development into gas stations, which are located in Atwater and Merced, Northern California, and which had an agreed upon value of approximately $2.6 million. One of these vacant land sites was contributed through the transfer of a 75% membership interest in a limited liability company that owns the vacant land site located in Northern California, in which profits and losses are allocated 75% to the Company and 25% to the noncontrolling member subject to a preferred equity split in which the noncontrolling member earns the first 10% of net profits and the balance of the 90% is to be paid along the terms of the 75% split to the Company and 25% to the noncontrolling member. The Contributor then completed the acquisitiontransfer to the Acquiror of its 17.9% passive interest in a limited liability company that is constructing a single family residential development located in Los Lunas, New Mexico (the “Avalon Property”) on June 26, 2017.

This residential development in New Mexico consisted of 251, non-contiguous, single family residential lots and a 10,000 square foot club house. 37 of the lots had been finished, and the remaining 214 were platted and engineered lots. The agreed upon value of its share of this property was approximately $7.4 million.


In return for the Contributed Properties, the Company issued to the Contributor 879,234 duly authorized, fully paid and non-assessable shares of the Company’s common stock, par value $0.01 per share (the “Common Stock”), which represented approximately 19.9% of the Company’s issued and outstanding Common Stock immediately prior to the Initial Closing, at an agreed upon Per Share Value (defined below) of $2.5183, or $2,214 in the aggregate. These shares of Common Stock are restricted and unregistered. The Company issued the remaining $7,786 of the approximately $10 million agreed upon consideration to the Contributor in the form of 123,668 shares of the Company’s newly designated non-voting Series A Convertible Preferred Stock, par value $0.01 per share (the “Series A Stock” or “Convertible Series A Preferred Stock”). Each share of the Series A Stock is convertible into 25 shares of the Company’s Common Stock, subject to the satisfaction of certain conditions, including stockholder approval in accordance with the rules of The Nasdaq Stock Market (“Nasdaq”), which was obtained on October 12, 2017. The shares of Series A Stock do not have voting rights and are restricted and unregistered. The number of shares of Common Stock issued to the Contributor and to be issued upon conversion of the Series A Stock was determined by dividing the $10 million agreed upon value of the Contributed Assets by $2.5183, a specified price per share value which represents a 7.5% premium above the volume-weighted average price (“VWAP”) of all on-exchange transactions in the Company’s Common Stock executed on Nasdaq during the forty-three trading days prior to the trading day immediately prior to the public announcement of the transaction by the Company and the Contributor Parent, as reported by Bloomberg L.P. (the “Per Share Value”). The shares of Common Stock both issued to the Contributor and issuable upon the conversion of the Series A Stock carry certain registration rights as specified in a Registration Rights Agreement dated May 17, 2017.

At the Initial Closing, the Company assumed the liabilities associated with the Contributed Properties, except that it did not assume any liabilities with respect to the Avalon Property until that property’s contribution was completed on June 26, 2017. The obligations that the Acquiror assumed at the Initial Closing include the following: Obligations of the Contributor and its affiliates under certain agreements covering the contributed properties, including an Operating Agreement of Central Valley Gas Station Development, LLC, a Delaware limited liability company, dated January 28, 2013, and all amendments thereto; and a Construction Contract dated November 19, 2014 between Central Valley Gas Stations Development, LLC, as owner and First Capital Builders, LLC, as Contractor, with respect to the project known commonly as Green Sands and Buhach Rd., Atwater, CA. Once the full interest in the Avalon Property was contributed to the Company, the Company also assumed the Operating Agreement of Avalon Jubilee, LLC, a New Mexico limited liability company dated as of May 16, 2012, and all amendments thereto; and a Development Services Agreement dated September 15, 2015 by and between UR-FC Contributed Assets, LLC, a Delaware limited liability company, as Owner, and Land Strategies, LLC, a Nevada limited liability company, as Developer, with respect to real property owned by Avalon Jubilee, LLC. As of the Initial Closing, the Company also assumed an installment note dated April 7, 2015 made by First Capital Real Estate Investments, LLC (“FCREI”) in favor of George Zambelli (“Zambelli”) in the original principal amount of $470 (the “Note”) and a Long Form Deed of Trust and Assignment of Rents dated April 7, 2015 between FCREI, as Trustor, Fidelity National Title Company, as Trustee (“Trustee”), and Zambelli, as Beneficiary (the “Deed of Trust”), which secures the Note (see also Note 12).

Second Contribution

Contributor Parent was also required to contribute two additional property interests valued at the agreed upon value amount of $20 million if certain conditions as set forth in the Contribution Agreement are satisfied by December 31, 2017. This second installment was mandatory under the original terms of the Contribution Agreement. As discussed below, the contribution Agreement was terminated and this second contribution did not take place.

The agreement stated that Contributor Parent must contribute to the Acquirer its 100% ownership interest in a private hotel that was currently undergoing renovations to convert to a Wyndham Garden Hotel. This 265 room full service hotel was located in Amarillo, Texas and had an agreed upon value of approximately $16 million and outstanding loans of approximately $10.11 million. Before contributing the property to the Acquiror, Contributor Parent was required to resolve a lawsuit concerning ownership of the property. Only when Contributor Parent had confirmed that it was the full and undisputed owner of the property was it able to contribute that interest to the Acquiror. If the contribution was made, the Company would have been required to account for this transaction as a business combination under ASC 805, Business Combinations.

On July 3, 2017, the Company and the Acquiror entered into an Agreement to Waive Second Closing Deliverables (the “Second Waiver”) with the Contributor Parties, amending the Contribution Agreement. The Contributor Parties had received an offer to purchase the Amarillo Hotel from a non-related third party. Under the Second Waiver, the Company and the Acquiror agreed to waive the requirement for the Contributor Parties to contribute to the Acquiror their 100% ownership interest in the Amarillo Hotel, and to accept in its place a contribution in cash of not less than $5.89 million from the Contributor Parties from the sale proceeds of the Amarillo Hotel, after the satisfaction of the outstanding loan, provided that the sale is completed and closed upon not later than August 31, 2017. In exchange the Contributor Parties would receive shares of stock in the Company, such amount to be calculated as set forth in the Second Waiver and Contribution Agreement. The sale of the Amarillo Hotel was not completed and closed by August 31, 2017, therefore the waiver of the requirement for the contribution of the interest in the Amarillo Hotel lapsed.


On September 22, 2017, the Company and Acquiror entered into a Second Agreement to Waive Closing Deliverables (the “Second Agreement”) with the Contributor Parties, amending the Contribution Agreement. Pursuant to the terms of the Second Agreement, the Company and the Acquiror agreed to extend the date for the closing of the sale of the Amarillo Hotel until October 18, 2017, with the contribution of the funds from the sale to be made not later than October 23, 2017. In exchange the Contributor Parties would receive shares of stock in the Company, such amount to be calculated as set forth in the Contribution Agreement, as amended by the Second Waiver and the Second Agreement. If the sale of the Amarillo Hotel was not completed and closed by October 18, 2017, the waiver of the requirement for the contribution of the interest in the Amarillo Hotel would lapse. The sale was not completed.

In addition, the agreement stated that Contributor Parent must contribute to the Acquiror its interest in Dutchman’s Bay and Serenity Bay (referred to as the “Antigua Resort Developments”), two planned full service resort hotel developments located in Antigua and Barbuda in which Contributor Parent would contribute a 75% interest in coordination with the Antigua government. Serenity Bay is a planned five star resort comprised of five contiguous parcels (28.33 acres) zoned for hotel and residential use that are planned for 246 units and 80 one, two and three bedroom condo units. Dutchman’s Bay is a planned four star condo hotel with 180 guestrooms, 102 two bedroom condos, and 14 three bedroom villas. For the property in Antigua, Contributor Parent was required to obtain an amendment to its agreement with the government to extend the time for development of these properties and confirm that all development conditions in the original agreement with the government had been either satisfied or waived.

In exchange for each of these properties, the agreement stated the Company would issue to Contributor a number of duly authorized, fully paid and non-assessable shares of the Company’s Common Stock or Series A Convertible Preferred Stock, determined by dividing the $20 million agreed upon value of that contribution by the Per Share Value. The agreement stated that shares would be comprised entirely of shares of Common Stock if the issuance had been approved by the Company’s stockholders prior to the issuance thereof and would be comprised entirely of shares of Series A Convertible Preferred Stock if such approval had not yet been obtained.

The Company had determined in accordance with the updated guidance of ASU 2017-01,Business Combinations (Topic 805) Clarifying the Definition of a Businessthat the Amarillo property (an operating hotel) represented a business as it included an organized workforce with the necessary skills, knowledge and experience to perform the acquired process and an input that the workforce could develop or convert into output. However, it was determined that the Antigua property did not represent a business. Based on the above conclusion it was determined that the Amarillo property component was not required to be analyzed under the provisions of ASC 815-10 “Derivatives and Hedging”since such contract between an acquirer and a seller to enter into a business combination are scoped out from its provisions. As for the Antigua property it was determined that such future transaction did not constitute a derivative instrument in accordance with ASC 815-10 -Derivatives and Hedging as the net settlement criteria was not met. Further, the Company considered the provisions of Subtopic ASC 815-40 “Contracts in the Entity’s Own Equity” and determined that such contractual obligations cannot be considered as indexed to an entity’s own stock, as its settlement provisions are not based on a fixed monetary amount or a fixed amount of a debt instrument issued by the entity but rather on the fair value of the Antigua property which represents a real estate asset. Based on the terms of this component, (i.e. the fair value of the Antigua property and the fair value of the shares that the Company is obligated to issue for this asset), it was determined that such freestanding financial instrument represented a financial asset required to be measured upon initial recognition of LCA-Vision,at fair value. Subsequent to initial recognition the financial instrument (which might be a previously publicly-traded Delaware corporation.

LCAfinancial asset or a financial liability depending on the fair value of its settlement terms) is required to be re-measured at fair value, with changes in fair value reported in earnings (within the line item “Revaluation of asset contribution related financial instrument, net”).

Optional Contribution

Contributor Parent had the option to contribute either or both of two additional property interests valued at the agreed upon value of $66.5 million if certain conditions as set forth in the Contribution Agreement were satisfied by December 31, 2017. This third installment was optional in Contributor Parent’s sole discretion. As discussed below, the contribution Agreement was terminated and this optional contribution did not take place.

The agreement stated that the Contributor Parent may contribute to the Acquiror its interest in a providerresort development project on an island just south of fixed-site laser vision corrections servicesHilton Head, South Carolina (“Melrose”). Contributor Parent had the property under a Letter of Intent and expected to close on the property by December 31, 2017. Melrose was valued by Contributor Parent at its LasikPlus® vision centers. an agreed upon value of $22.5 million, based upon a senior lending position that Contributor Parent held under the Letter of Intent on this property.


The vision centers provideagreement stated that the staff, facilities, equipmentContributor Parent also may contribute to the Acquiror a golf and support servicessurf club development project on the Baja Peninsula in Mexico (“Punta Brava”). Contributor Parent also had this property under a Letter of Intent and expected to close by December 31, 2017. Punta Brava was valued at the agreed upon value by Contributor Parent at $44 million based on Contributor Parent’s commitment of $5 million upon closing on this property, plus a commitment for performing laser vision correctionan additional $5 million and a second commitment of $34 million for construction of the project.

In exchange for each of these properties, the Company would issue to Contributor a number of duly authorized, fully paid and non-assessable shares of the Company’s Common Stock or Series A Convertible Preferred Stock, determined by dividing an agreed upon value of $86,450 (130% of the value of the agreed upon value of $66,500) by the Per Share Value. The shares would be comprised entirely of shares of Common Stock if the issuance had been approved by the Company’s stockholders prior to the issuance thereof and would be comprised entirely of shares of Series A Convertible Preferred Stock if such approval had not yet been obtained. In addition, the Company would issue to Contributor a five year warrant (the “Warrant”) to purchase up to 25,000,000 shares of the Company’s Common Stock at an exercise price of $3.00 per share that employs advanced laser technologieswould vest with respect to help correct nearsightedness, farsightednessthe number of underlying shares upon the achievement of the milestone specified in the Contribution Agreement. The number of warrant shares and astigmatism.the exercise price would be equitably adjusted in the event of a stock split, stock combination, recapitalization or similar transaction. These optional contributions represented a potential liability to the Company as the number of shares and warrants to be issued is fixed but the market value of the shares fluctuates. It is possible that the share price could have risen to a level that upon contribution of the properties causing the Company to give consideration that exceeded the fair value of the assets acquired. This would represent a potential liability to the Company and to quantify the liability the Company has used the Black Scholes formula. The vision centers are supported by independent ophthalmologists and credentialed optometrists,warrants also represented a potential liability in that the Company may be required to issues shares at $3 when the share price was significantly higher.

To estimate the fair value of the liability associated with optionality granted to the Contributor as well as other healthcare professionals. Substantially all of LCA's revenues are derived from the delivery of laser vision correction procedures performedwarrant liability, Management has used the Black Scholes option pricing formula. The key input in the vision centers.

F-21

The purchase pricecalculation is the assumption of LCA-Visionhow volatile the Company stock was $106,552 in aggregate consideration, paid in cash (includingto be over the full uselife of the credit facility), consisting of:option. The more volatile the Company is expected to be, the greater its potential liability.  Future volatility is unknown, as such Management had used a volatility proxy of 39.45% which equaled the average volatility of stocks in the Company’s forward looking peer group of Real Estate Development at that time.  After the calculation is performed, additional factors must be considered. It is possible that despite being economically rational to contribute the properties based on the Company stock price relative to the value of the optional properties, the Contributor may not have the ability to contribute. Therefore a 50% discount was applied to the option value produced by the Black Scholes formula to arrive at final liability value for the optionality component. The warrants received a further 50% discount as they contained a vesting schedule with milestones that must be achieved by the Contributor once the property was contributed. With the expiration of the agreement on December 31, 2017, the fair value of the liability was $0.

The Company has determined that the Company’s contractual obligations under the optional contributions does not constitute a derivative instrument in accordance with ASC 815-10 -Derivatives and Hedging as the net settlement criteria is not met. Further, the Company considered the provisions of Subtopic ASC 815-40Contracts in the Entity’s Own Equity and determined that such contractual obligations cannot be considered as indexed to an entity’s own stock, as its settlement provisions are not based on a fixed monetary amount or a fixed amount of a debt instrument issued by the entity but rather on the fair value of certain real estate assets. Thus, such freestanding financial instrument were classified as financial liabilities and were measured upon initial recognition at fair value. Subsequent to initial recognition the financial liabilities are remeasured at fair value, with changes in fair value reported in earnings (within the line item “Revaluation of asset contribution related financial instruments, net”).

The Company elected to early adopt ASU 2017-01 Business Combinations (Topic 805)Clarifying the Definition of a Business.Accordingly, the determination whether the asset contribution transaction represents a business combination was evaluated by applying the ASU 2017-01 guidance. The Company has determined that the group of assets assumed in the First Contribution does not (and also, none of them on a stand-alone basis) include, an input and a substantive process that together significantly contribute to the ability to create output and thus it was determined that the First Contribution represents an acquisition of assets rather than a business combination. Accordingly, the total sum of the fair value of consideration given (i.e. the fair value of the equity interests issued) together with the transaction costs and the fair value of financial assets was allocated to the individual assets acquired and liabilities assumed in the first contribution based on their relative fair values at the date of acquisition. Such allocation did not give rise to goodwill.


Fair value LCA-Vision stock (A) $103,896 
Fair value of LCA-Vision restricted stock units, including payroll taxes (B)  2,656 
Total purchase price $106,552 

The consideration for the assets acquisition as of the Initial Date consists of the following:

Fair value 879,234 shares of FC Global common stock (*) $1,275 
Fair value 123,668 shares of FC Global Series A preferred stock (*)  4,483 
Fair value of financial liability related to Optional contribution (**)  857 
Fair value of Warrant (***)  1,925 
Fair value of asset related to future mandatory asset contribution (***)  (4,175)
Fair value of assumed note payable on acquired asset  470 
Transaction costs  283 
Total consideration $5,118 

A.Based(*)Fair value of Common shares based on 19,347,554 outstandingquoted market price on date of transaction and Fair value of preferred shares based on the number of LCA-Vision common stock at May 12, 2014.
B.Basedshares to which they can be converted on 476,436 outstanding or deemed to be outstanding restricted stock units of LCA-Vision common stock at May 12, 2014.the transaction date
(**)Related to Optional Contribution
(***)Related to Second Contribution

The fair value of the assets acquired, and liabilities assumed were based on management estimates and values, derived from an outside independent appraisal. The Company expected thatincluding estimates based on historical sales of similar parcels. Adjustments were applied to such historical sales and assumptions were applied to other attributes of the allocation would be finalized within twelve months after the merger. However, LCA was soldassets in January 2015 and it is presented as a discontinued operations, see Note 2. Accordingly management has determinedorder to retain the provisional amounts. Based on the purchase price allocation, theestimate market value. The following table summarizes the provisional fair value amountsallocation of the consideration to the assets acquired in the transaction.

The allocation of aforesaid total consideration is as follows:

Investment properties $2,600 
Investment in other company  2,668 
Less: Noncontrolling interest (***)  (150)
Total assets acquired at fair value $5,118 
Impairment of investment in other company (*)  (862)
Total asset value as of December 31, 2017 $4,256 

(*) Loss from impairment was recorded amounting to $862 as part of operating expenses in the Company’s consolidated statement of comprehensive loss during the year ended December 31, 2017 (see also Note 13).

(***) Attributable to the 25% noncontrolling membership interest in a limited liability company that owns a vacant land site located in Northern California

The fair value of options, warrants and liabilities assumedasset related to future mandatory asset contribution granted was estimated at the dateInitial Date by using the Black-Scholes option pricing model. The following are the data and assumptions used:

Options Value:

May 17, 2017
Dividend yield (%)0
Expected volatility (%)39.45
Risk free interest rate (%)1.25
Strike price1.93
Stock price1.45
Probability (%)50
Expected term of options (years)0.62

Warrants Value:

May 17, 2017
Dividend yield (%)0
Expected volatility (%)39.45
Risk free interest rate (%)1.25
Strike price3
Stock price1.45
Probability (%)50
Expected term of options (years)5


Asset related to future mandatory asset contribution:

May 17, 2017
Dividend yield (%)0
Stock price1.45
Probability (%)70

As of acquisition:

Cash and cash equivalents $29,042 
Current assets, excluding cash and cash equivalents  6,114 
Deferred tax asset, current  1,124 
Property, plant and equipment  17,269 
Identifiable intangible assets  39,050 
Other assets  1,518 
Total assets acquired at fair value  94,117 
     
Current liabilities  (19,009)
Long-term debt  (1,603)
Deferred tax liability, long-term  (9,138)
Other long-term liabilities  (7,397)
Total liabilities assumed  (37,147)
     
Net assets acquired $56,970 
The purchase price exceededDecember 31, 2017, neither the Secondary nor the Optional Contribution were made and the Contribution Agreement was terminated at that date. Consequently, as of December 31, 2017, the fair value of the asset contribution related to aforementioned financial instruments was reduced to $0. During the period from the closing of the Initial Date and until December 31, 2017, the Company has recognized a net loss as revaluation of the fair value of asset contribution related financial instruments in the total amount of $1,392.

Note 6

Inventories, net:

  December 31, 
  2017  2016 
Raw materials and work-in-process $  $1,968 
Finished goods     5,368 
Total inventories $  $7,336 
Less assets held for sale (*)     (7,336)
Total inventory $  $ 

(*) Inventory was classified as part of the assets acquired by $49,582, whichheld for sale as of December 31, 2016. In January 2017, all of the consumer inventory was recorded as goodwill. The goodwillsold to ICTV (see also Note 2 and 4).

Note 7

Property and Equipment, net:

  December 31, 
  2017  2016 
Equipment, computer hardware and software $320  $5,005 
Furniture and fixtures  350   433 
Leasehold improvements  112   438 
   782   5,876 
Accumulated depreciation and amortization  (777)  (4,888)
Total property and equipment, net $5  $988 
Less Assets held for sale (*)     (911)
Total property and equipment, net $5  $77 

(*) In January 2017, the consumer division property and equipment was recognized at that time as a new reportable segmentsold to ICTV (see also Note 2 and allocated to the activities of LCA.4).


The summarized unaudited pro-forma results for

During the years ended December 31, 20142017 and 2013 are not provided as required under ASC Topic 805 since LCA is presented as a discontinued operation for the periods presented.

2016, depreciation expenses were $178 and $292, respectively.

Note 4

Inventories:
  December 31, 
  2014  2013 
Raw materials and work-in-process $7,483  $12,631 
Finished goods  11,897   
14,916
 
Total inventories $19,380  $27,547 
Work-in-process is immaterial given the typically short manufacturing cycle, and therefore is disclosed in conjunction with raw materials.
F-22

Note 5
Property and Equipment:
  December 31, 
  2014  2013 
Lasers-in-service $18,974  $12,599 
Equipment, computer hardware and software  4,870   4,730 
Furniture and fixtures  767   705 
Leasehold improvements  481   534 
   25,092   18,568 
Accumulated depreciation and amortization  (11,290)  (8,079)
Total property and equipment, net $13,802  $10,489 

Related depreciation and amortization expense was $3,657 in 2014, $2,875 in 2013 and $2,367 in 2012.
Note 6
8

Patents and Licensed Technologies, net:

  December 31, 
  2014  2013 
Gross Amount beginning of period $15,648  $15,411 
Additions  168   171 
Translation differences  (190)  66 
Gross Amount end of period  15,626   15,648 
         
Accumulated amortization  (6,815)  (4,816)
         
Net Book Value $8,811  $10,832 
Related amortization expense was $2,055, $2,043 and $2,049 for

  December 31, 
  2017  2016 
Gross Amount beginning of period $  $3,376 
Disposals     (177)
Translation differences     36 
Gross Amount end of period     3,235 
         
Accumulated amortization     (1,974)
Impairment of assets (see Note 9 below)     (1,261)
         
Total patents and licensed technology $  $ 

During the years ended December 31, 2014, 20132017 and 2012,2016, amortization expenses were $0 and $230, respectively. An amount of $13,500, included in gross amount related to Patents represents product and core technologies recorded as part of the purchase price allocation done in connection with the reverse acquisition of the Pre-merged PhotoMedex.

Estimated amortization expense for amortizable patents and licensed technologies assets for the next five years is as follows:
2015 $2,056 
2016  2,019 
2017  903 
2018  906 
2019  892 
Thereafter  2,035 
Total $8,811 

Note 7

9

Goodwill and Other Intangible Assets:

As part of the purchase price allocation for thea reverse acquisition transaction in 2011, the Company recorded goodwill in the amount of $24,005 and definite-lived intangibles in the amount of $12,000. Goodwill reflects the value or premium of the acquisition price in excess of the fair values assigned to specific tangible and intangible assets. Goodwill has an indefinite useful life and therefore is not amortized as an expense but is reviewed annually for impairment of its fair value to the Company. Activity in goodwill during the year ended December 31, 2016 was as follows:

Balance at January 1, 2016 $3,581 
Disposal on sale of assets  (1,039)
Impairment of goodwill  (2,257)
Translation differences  (285)
Balance at December 31, 2016 $ 

The purchase price intrinsicallyfair value of Goodwill associated with the operating and reporting units were estimated using a combination of Income and Market Approach methodologies to valuation. The Income method of valuation explicitly recognizes the current value of future economic benefits developed by discounting future net cash flows to their present value at a rate that reflects both the current return requirements of the broadened depthmarket and the risks inherent in the market. The Market approach measures the value of an asset through the analysis of recent sales or offerings of comparable property.

The Company’s business was organized into three operating and reporting units which are defined as Consumer, Physician Recurring, and Professional Equipment.

During the third quarter of 2016, we recorded goodwill and other intangible asset impairment charges of $3,518, as we determined that a portion of the management team and the addition of a sizeable direct sales force creating greater access to the physician community with branded products and technologies. Furthermore, the purchase price paid by Radiancy, Inc., a private company includes, among other things, other benefits such as the intrinsic value of being a Nasdaq-listed issuer post mergerthe Company’s goodwill and now having access to capital markets and stockholder liquidity.


F-23

   
Balance at January 1, 2014 $24,930 
Additions to goodwill  - 
Translation differences  (882)
Balance at December 31, 2014 $24,048 
other intangible assets was impaired in connection with the then pending transaction with ICTV Brands, Inc. (See also Note 1). The Company has no accumulatedrecorded an impairment lossesof the entire remaining balance of Consumer segment goodwill in the amount of $2,257 and recorded the impairment of the Consumer segment of the intangibles for its licensed technology in the amount of $1,261. During the year ended December 31, 2016 the Company derecognized an amount of $1,039 of goodwill related to the continuing operationsPhysician Recurring segment in connection with the asset sale of the Neova product line. All such impairment changes are included in discontinued operations.


Note 10

Accrued Compensation and related expenses:

  December 31, 
  2017  2016 
Accrued payroll and related taxes $453  $262 
Accrued vacation  14   66 
Accrued commissions and bonuses (*)     3,701 
Total accrued compensation and related expense $467  $4,029 

(*)The amount related to the obligation the Company had in connection with the Payout Notes Holders as of December 31, 2016. On December 22, 2017, the then outstanding payout notes were converted into shares of common stock of the Company (see also Note 14).

Note 11

Other Accrued Liabilities:

  December 31, 
  2017  2016 
Accrued taxes, including liability for unrecognized tax benefit, (see also Note 15) $1,549  $1,606 
Other accrued liabilities  901   4,417 
Total other accrued liabilities $2,450  $6,023 

Note 12

Note payable:

Following the Initial Closing of the Interest Contribution Agreement (see also Note 5), the Company assumed an installment note dated April 7, 2015 made by the Contributor in favor of George Zambelli (“Zambelli”) in the original principal amount of $470 (the “Note”) and a Long Form Deed of Trust and Assignment of Rents dated April 7, 2015 between FCREI, as Trustor, Fidelity National Title Company, as Trustee (“Trustee”), and Zambelli, as Beneficiary (the “Deed of Trust”), which secures the Note. The Note carries a per annum interest rate of 8% which is payable on a monthly basis from the Initial Closing. As of December 31, 2014. See 2017, the Note 2 regarding impairmentamounted to $459 ($454 out of goodwill allocated to the discontinued operations.


which is classified as non-current note payable) and has a maturity date of April 10, 2020.

Note 13

Commitments and Contingencies:

Leases

The goodwill was allocated among the reportable segments as ofCompany has entered into a non-cancelable operating lease agreement for real property which expires on December 31, 2014 in accordance with the provisions of ASC Topic 350-20 Intangibles-Goodwill and consisted of the following:

  December 31, 2014 
   
Consumer segment $19,968 
Physician Recurring segment  4,080 
Total goodwill $24,048 
Set forth below is a detailed listing of other definite-lived intangible assets:
  December 31, 2014  December 31, 2013 
  Trademarks  Customer Relationships  Total  Trademarks  Customer Relationships  Total 
Gross Amount beginning of period $5,772  $6,417  $12,189  $5,744  $6,372  $12,116 
Translation differences  (80)  (128)  (208)  28   45   73 
Gross Amount end of period  5,692   6,289   11,981   5,772   6,417   12,189 
                         
Accumulated amortization  (1,731)  (1,913)  (3,644)  (1,178)  (1,310)  (2,488)
                         
Net Book Value $3,961  $4,376  $8,337  $4,594  $5,107  $9,701 
Related amortization2018. Rent expense was $1,200, $1,200$188 and $1,212$550 for the years ended December 31, 2014, 20132017 and 2012. Customer Relationships embody the value2016 respectively. The future annual minimum payment under this lease, relating to the Company of relationships that Pre-merged PhotoMedex had formed with its customers. Tradename includes the names and various other trademarks associated with Pre-merged PhotoMedex products (e.g. "XTRAC", "Neova" "Omnilux" and "Lumiere").
Estimated amortization expense for the above amortizable intangible assets for the next five years isCompany’s continuing operations are as follows:
2015 $1,200 
2016  1,200 
2017  1,200 
2018  1,200 
2019  1,200 
Thereafter  2,337 
Total $8,337 

Year Ending December 31,   
     
2018 $70 


F-24

Note 8
Accrued Compensation and related expenses:
  December 31, 
  2014  2013 
Accrued payroll and related taxes $513  $707 
Accrued vacation  211   290 
Accrued commissions and bonuses  1,898   2,233 
Total accrued compensation and related expense $2,622  $3,230 
Note 9
Other Accrued Liabilities:
  December 31, 
  2014  2013 
Accrued warranty, current, see Note 1
 $665  $1,094 
Accrued  taxes, including liability for unrecognized tax benefit, see Note 13
  1,362   1,023 
Accrued sales return (1)  7,651   16,046 
Other accrued liabilities  3,344   3,869 
Total other accrued liabilities $13,022  $22,032 
(1)The activity in the sales returns liability account was as follows:
  December 31, 
  2014  2013 
     
Balance at beginning of year $16,046  $11,901 
Additions that reduce net sales  35,771   47,916 
Actual returns  (44,166)  (43,771)
Balance at end of year $7,651  $16,046 
Note 10
Long-term Debt:
In the following table is

As a summaryresult of the Company's long-term debt:

  December 31, 
  2014  2013 
     
Senior-secured credit facilities $76,500  $- 
Term note  -   10,000 
Sub-total  76,500   10,000 
Less: current portion  38,732   10,000 
Long-term debt $37,768  $- 
Senior Secured Credit Facilities
On May 12, 2014,sale of the Consumer Products division to ICTV Brands, the Company no longer had a need for certain of its leased properties, including the facilitates located in the United Kingdom and in Israel. In connection with the Transition Services Agreement entered into an $85 million senior secured credit facilities ("the Facilities") with JP Morgan Chase ("Chase") which included a $10 million revolving credit facility and a $75 million four-year term loan. The facilities were utilized to refinance the existing term debt with Chase, fund the acquisition of LCA and for working capital and other general corporate purposes.
F-25


Interest is determined at Eurodollar plus a margin between 3.25% and 4.50%. The margin is updated quarterly based on the then-current leverage ratio. The facilities are secured by a first priority security interest in and lien on all assets of the Company. All current and future subsidiaries are guarantors on the facilities. There are financial covenants including; a maximum leverage covenant and a minimum fixed charge covenant, which the Company must maintain. These covenants will be determined quarterly based onand ICTV, the Company maintained certain of its leased properties for a rolling past four quartersspecified period of financial data.time to allow ICTV to transition its operations to its own facilities. Leases that expired during that transition period were not renewed. As of December 31, 2014,2017, the Company continued to fail to meet both financial covenantsterminated the leases in Israel and is in default of the credit facilities
On August 4, 2014, the Company received a notice of default and a reservation of rights from Chase and engaged a third-party independent advisor to assist the Company in negotiating a longer term solution to the defaults. The parties had entered into an initial Forbearance Agreement (the "Initial Forbearance Agreement") on August 25, 2014. On November 4, 2014, the Company entered into an Amended and Restated Forbearance Agreement (the "Amended Forbearance Agreement") with the lenders that are parties to the Credit Agreement and with Chase, as Administrative Agentearly surrender agreement for the Lenders.
Effective February 28, 2015, the Company entered into a Second Amended and Restated Forbearance Agreement (the "Second Amended Forbearance Agreement") with the lenders (the "Lenders")United Kingdom facility that are parties to the Credit Agreement dated May 12, 2014, and with JP Morgan Chase, as Administrative Agent for the Lenders.
Pursuant to the terms of the Second Amended Forbearance Agreement, the Lenders have agreed to forbear from exercising their rights and remedies with respect to the Specified Events of Default from August 25, 2014 until April 1, 2016, or earlier if an event of default occurs (the "Forbearance Period"). Chase and the Lenders agreed that the Company shall not be obligated to pay the principal amounts set forth in Section 2.08(b) of the Credit Agreement for any date identified therein during the period beginningwas consummated on February 28, 2015 and ending on the end of the Forbearance Period (the "Effective Period"), and that any failure to do so shall not constitute a default or event of default.  Instead, the Lenders and the Company agreed that the Company would make prepayments against the Term Loan of $250,000 on the first business day of each month during the Forbearance Period, which will be applied in direct order of maturity. October 17, 2017.

Litigations

JFURTI

The Company also agreed that, on or before the fifth calendar day of each month, the Company would pay against the Term Loan $125,000is a party to the extent that the cash-on-hand exceeds $5 million, and 100% of the cash-on-hand in excess of $7 million, also to be applied to the Term Loan in inverse order of maturity.

Under the provisions of the Second Amended Forbearance Agreement, the Company will not have to comply with certain financial covenants contained in Section 6.11 of the Credit Agreement for the Forbearance Period, and that any failure to do so shall not constitute a default or event of default.  However, the Company will have to meet certain minimum EBITDA targets (as defined in the forbearance agreement) for the quarters ending March 31, 2015, June 30, 2015, September 30, 2015 and December 31, 2015.
Pursuant to the Second Amended Forbearance Agreement, all loans under the Facilities shall, beginning November 1, 2014, bear interest at the CB Floating Rate (as defined in the Credit Agreement) plus 4.00%. Additionally, following the occurrence and continuance of any default or event of default (other than a Specified Event of Default), the Company's obligations under the Facilities shall, at the option of Chase and the Lenders, bear interest at the rate of 2.00% plus the rate otherwise in effect.
The Company and its subsidiaries have also agreed not to pay in cash any compensation to the either the Company's Chief Executive Officer or President that is based on a percentage of sales or another metric other than those officer's base salary, perquisites and standard benefits provided to or on behalf of those executives under the terms of their employment agreements. Those payments may be accrued or deferred and paid in cash only after the repayment of the Facilities in full.
The Company has agreed to provide, on or before May 29, 2015, a strategic business plan for the overall direction of the Company's and its subsidiaries' businesses, including projected income statements, balance sheets, schedules of cash receipts and cash disbursements, payments and month-end balances, and detailed notes and assumptions, projected on a monthly basis through April 1, 2016. The Company has also agreed to provide quarterly updates to that plan by August 31, 2015, November 30, 2015 and February 29, 2016.
F-26


The Company continues to retain the services of both Getzler Henrich & Assoc.JFURTI, LLC, a third-party independent business advisor, as well as Canaccord Genuity, Inc., a banking and financial services company, and has also retained the services of Nomura Securities International, Inc., also a banking and financial services company. During the Forbearance Agreement, the Company and these advisors will continue to prepare and distribute offering memoranda and other marketing materials to prospective lenders with regard to a proposed credit facility for the Company, the proceeds of which would be in an amount sufficient to repay in full and in cash the Company's remaining obligations under the Facilities, and to explore other strategic alternatives. The closing of any such refinancing or alternative arrangement would occur no later than the end of the Forbearance Period.
The Company agreed to limit certain capital expenditures to $100,000 per quarter, except for those involving the Company's XTRAC® or VTRAC® medical devices, and will not make investments or acquire any other interests in affiliated companies except as agreed to by the Lenders.
As consideration for the Lender's entry into the Second Amended Forbearance Agreement, the Company has agreed to pay the Lenders certain forbearance fees (the "Forbearance Fees"), which are payable on the last business day of each of the specified months: for May and June 2015, $750,000 each month; for July through September 2015, $1,000,000 each month; for October through December 2015, $1,250,000 each month; and for January through March 2016, $1,500,000 each month. However, should the Company complete a capital transaction acceptable to the Lenders that reduces the then-outstanding principal balance of the Term Loan to less than $10 million and repays all Forbearance Fees accrued and unpaid to that date, the monthly Forbearance Fee for the remainder of the Forbearance Period shall be earned and accrued in an amount that is 50% of the amount specified for each of the remaining months. In addition, the $500,000 Forbearance Fee set forth in Section 4.10(b) of the Amended Forbearance Agreement remains due and payable to the Lenders on the earlier of the Expiration Date or the Termination Date of the Forbearance Period. All Forbearance Fees are considered earned and are included in the Obligations under the Credit Agreement.
The Second Amended Forbearance Agreement is also subject to customary covenants, including limitations on the incurrence of or payments on indebtedness to other persons or entities and requirements that the Company provide periodic financial information and information regarding the status of outstanding litigation involving the Company and its subsidiaries to the Lenders.
In addition, the unamortized related debt issue costs and debt discount of $2,358 have been expensed during the year ended December 31, 2014.
Term-Note Credit Facility
In December 2013, the Company, through its subsidiary, Radiancy, Inc., entered into a term-note facility with JP Morgan Chase ("Chase"). The facility had maximum principal amount of $15 million and was for a term of one year. As of December 31, 2013, the Company had total borrowings of $10 million under this facility. The stated interest rate for any draw under the credit facility was set as the greater of (i) prime rate, (ii) federal funds effective rate plus .5% or (iii) LIBOR plus 2.5%. Each draw has a repayment period of one year with principal due at maturity, although any draw may be paid early with penalty. This term-note was cancelled at the time the senior secured credit facilities were entered into.
The following table summarizes the future minimum payments that the Company expects to make for long-term debt:
2015 $38,732 
2016  37,768 
  $76,500 

F-27


Note 11
Commitments and Contingencies:
Leases
The Company has entered into various non-cancelable operating lease agreements for real property and one minor operating lease for personal property. These arrangements expire at various dates through 2017. Rent expense was $4,708 (including $3,690 from LCA), $1,002 and $908 for the years ended December 31, 2014, 2013 and 2012, respectively. Not included in the table below is $17,916 related to LCA, which was sold as of January 31, 2015. The future annual minimum payments under these leases, relating to our continuing operations are as follows:
Year Ending December 31,  
2015 $814 
2016  472 
2017  176 
Thereafter  366 
Total $1,828 
Litigation
During the year ended December 31, 2013, Radiancy, Inc., a wholly-owned subsidiary of PhotoMedex, commenced legal action against Viatek Consumer Products Group, Inc., over Viatek's Pearl and Samba hair removal products which Radiancy believes infringe the intellectual property covering its no!no! hair removal devices. The first suit, which was filed in the United States Federal Court, Southern District of New York, includes claims against Viatek for patent infringement, trademark and trade dress infringement, and false and misleading advertising. A second suit against Viatek was filed in Canada, where the Pearl is offered on that country's The Shopping Channel, alleging trademark and trade dress infringement, and false and misleading advertising. Viatek's response contains a variety of counterclaims and affirmative defenses against both Radiancy and its parent company PhotoMedex, including, among other counts, claims regarding the invalidity of Radiancy's patents and antitrust allegations regarding Radiancy's conduct.
Radiancy, and PhotoMedex, had moved to dismiss PhotoMedex from the case, and to dismiss the counterclaims and affirmative defenses asserted by Viatek. On March 28, 2014, the Court granted the Company's motion and dismissed PhotoMedex from the lawsuit. The Court also dismissed certain counterclaims and affirmative defenses asserted by Viatek, including Viatek's counterclaims against Radiancy for antitrust, unfair competition, and tortious interference with business relationships and Viatek's affirmative defenses of unclean hands and inequitable conduct before the U.S. Patent and Trademark Office in procuring its patent. Radiancy also moved for sanctions against Viatek for failure to provide meaningful and timely responses to Radiancy's discovery requests; on April 1, 2014, the Court granted that motion. Viatek appealed both the sanctions ruling and the dismissal of Viatek's counterclaims and defenses from the case, as well as PhotoMedex's dismissal as a plaintiff; the Court has denied those appeals. The Court has appointed a Special Master to oversee discovery. A Markman hearing on the patents at issue was held on March 2, 2015. Viatek has requested an opportunity to supplement its patent invalidity contentions in the US case; Radiancy opposes that request. Radiancy has been granted permission by the US Court to supplement its earlier sanctions motion to include the legal fees and costs associated with preparing and prosecuting that motion. As of December 31, 2014, discovery and related court hearings continue in both the US and the Canadian cases. At this time, the amount of any loss, or range of loss, cannot be reasonably estimated as the case is still in the early stages of discovery to determine the validity of any claim or claims made by Viatek. Therefore, the Company has not recorded any reserve or contingent liability related to this particular legal matter. However, in the future, as the case progresses, the Company may be required to record a contingent liability or reserve for this matter. 
On December 20, 2013, PhotoMedex, Inc. was served with a class action lawsuitet al v. Suneet Singal, et al, filed in the United States District Court for the EasternSouthern District of Pennsylvania againstNew York.  The suit names as defendants Suneet Singal, an officer of various First Capital companies as well as the Company and its two top executives, Dolev Rafaeli,Company’s former Chief Executive Officer and Dennis M. McGrath, Presidentformer member of the Company’s Board of Directors,, Frank Grant and Chief Financial Officer. Richard Leider, board members of  First Capital Real Estate Investments, LLC, First Capital Real Estate Advisors, LP, Presidential Realty Corporation, Presidential Realty Operating Partnership, Downey Brand LLP and now the Company (under its previous name, PhotoMedex Inc.), as well as nominal derivative defendants First Capital Real Estate Trust Incorporated and First Capital Real Estate Operating Partnership, L.P. Mr. Leider is also on the Board of Directors of the Company.

The suit is the ninth filed by Jacob Frydman and/or JFURTI, LLC in a dispute between the plaintiffs and the First Capital group of companies, which entered into a series of agreements with Mr. Frydman beginning in September 2015. Mr. Frydman had founded, sponsored, and taken public United Realty Trust Incorporated, a Real Estate Investment Trust (“REIT”). Mr. Frydman was the CEO and Chairman of the REIT as well as the owner of various other United Realty branded companies affiliated with the REIT business. In September 2015, Mr. Frydman and Mr. Singal negotiated and agreed to a transaction between various First Capital branded companies, on the one hand, and the United Realty branded companies affiliated with the REIT business, on the other hand, as a result of which the REIT was rebranded as the Contributor Parent.

After the September 2015 transaction was concluded, several disputes arose between the parties. This suit is the ninth action brought by Mr. Frydman in state and federal courts relating to these disputes, and the second attempt by Mr. Frydman and JFURTI to bring federal claims derivatively in this Court against First Capital entities and other parties. The first action, titled JFURTI, LLC and Jacob Frydman v. Forum Partners Investment Management LLC et al., No. 16 Civ. 8633 (the “Prior Action”), commenced on November 7, 2016 and asserted, inter alia, derivative RICO and securities fraud claims. The Court dismissed the action in a decision and order dated April 27, 2017.

Following dismissal of the Prior Action, Mr. Frydman sent letters to each member of the Contributor Parent’s Board of Directors (the “Demand Letter”) demanding that the Board investigate and remediate the dissipation of assets as alleged by plaintiffs. In particular, the Demand Letter questioned (i) a letter of intent with Presidential Realty Corporation, or Presidential, announced in an 8K filed by First Capital REIT on or about July 18, 2016; (ii) First Capital REIT’s use of funds raised between September 15, 2015 and February 28, 2016; (iii) an interest contribution agreement with Presidential entered into on or about December 16, 2016; (iv) the Contributor Parent’s failure to file quarterly and annual reports; (iv) an interest contribution agreement entered into on March 31, 2017 with PhotoMedex; and (v) other purportedly fraudulent acts such as publishing an artificially inflated NAV, defaulting on certain mortgage loans, misrepresentations by Singal with respect to certain properties contributed to the REIT through the Master Agreement executed on September 15, 2015, and various loan agreements with Forum Partners Investment Management LLC, or Forum. The Demand Letter also demanded inspection of certain corporate documents pursuant to Md. Code § 2-512.

The Contributor Parent commenced such an investigation, and offered such an inspection, but Mr. Frydman and JFURTI failed to wait for the results of the investigation or make any inspection, and instead brought suit in the same court as the Prior Action. The suit alleges, among other claims, violations of the Federal securities laws between November 7, 2012 and November 14, 2013. A mediation on possible settlement of this action was held on November 10, 2014; the parties including the Company's insurance carrier have agreed on a possible settlement. The Company has paid its own legal fees up to the deductible cap on its insurance policy, and all amounts to be paid to plaintiffs and plaintiff's counsel will be paid by the carrier§ 10(b) of the insurance policy. This settlement is subject to reviewExchange Act and approval by the District Court, which has not yet rendered its opinion.

F-28


The Company was served on July 29, 2014 with an application to certify a class action, filed in Israel District CourtRule 10b-5 (1) against Mr. Singal and First Capital Real Estate Investments LLC for Tel Aviv against the Company and its two top executives, Dolev Rafaeli, Chief Executive Officer, and Dennis M. McGrath, President and Chief Financial Officer. The plaintiff's who initiated this complaint have agreed to be part of, and be bound by, the possible settlement reached in the United States District Court for the Eastern District of Pennsylvania against the Company and the same two top executives.
There were multiple class-action lawsuits filedmisrepresentations in connection with PhotoMedex's proposed acquisitionthe Master Agreement entered into on September 15, 2015 and related agreements; (2) against Downey Brand for failure to file certain deeds; (3) against First Capital defendants (except Grant and Leider), Forum defendants, and Presidential defendants for a fraudulent scheme to sell Contributor Parent assets to Presidential; and (4) against First Capital defendants, the Forum defendants, and the Company for the transfer of LCA-Vision, Inc. All cases assertedFirst Capital REIT and First Capital OP assets to the Company in exchange for allegedly worthless shares. There are also claims against LCA-Vision, Inc.,under state law for common law fraud, conversion, fraudulent conveyance, waste and a mixmismanagement, accounting, injunctive relief, and violation of other defendants, including LCA's chief executive officer and directors, PhotoMedex, and Gatorade Acquisition Corp., a wholly owned subsidiary of PhotoMedex. The complaints generally allege that the proposed acquisition undervalued LCA and deprived LCA's shareholdersCal. Bus. & Prof. Code § 17-200. Many of the opportunity to participateclaims asserted in LCA's long-term financial prospects, that the "go shop" and "deal-protection" provisionsComplaint, including the securities fraud claims, were never raised in the Demand Letter, as required by law. The suit seeks damages against all defendants for the failure of the Merger Agreement were designedREIT to prevent LCA from soliciting or receiving competing offers, that LCA's Board breached its fiduciary dutiesrespond to the Demand Letter, and failedan injunction against the sale of the assets to maximize that company's stockholder value, and that LCA, PhotoMedex, and Gatorade aided and abetted the LCA defendants' alleged breaches of duty. Presidential defendants.


The parties have reachedsubmitted a possible settlementmotion for an order (i) staying all proceedings in these suits,this action for 60 days, or until the end of 2017, and (ii) extending the defendants time to respond to the complaint, or to make a motion with respect to the complaint, until 45 days after First Capital REIT’s response to the Demand Letter. The Court granted that motion on October 31, 2017. Upon completion of their investigation, the Contributor Parent provided a response to the Demand Letter, denying all claims made in the letter. A Motion to Dismiss this action has now been filed with the Company contributing less than $100,000 to the settlement, plus the paymentCourt on behalf of its legal fees, and the remainder of the settlement being covered by the insurance carriers. This settlement is subject to review and approval by the state court, which has not yet rendered its opinion.

On April 25, 2014, a class action lawsuit was filed in the United States District Court for the District of Columbia against the Company's subsidiary, Radiancy, Inc. and Dolev Rafaeli, Radiancy's President. The suit was filed by Jan Mouzon and twelve other customers residing in ten different states who purchased Radiancy's no!no! Hair products. It alleges various violations of state business and consumer protection codes including false and misleading advertising, unfair trade practices, and breach of express and implied warranties. The complaint seeks certification of the putative class, or, alternatively, certification as subclasses of plaintiffs residing in those specific states. The complaint also seeks an unspecified amount of monetary damages, pre-and post-judgment interest and attorneys' fees, expert witness fees and other costs. Dr. Rafaeli was served with the Complaint on May 5, 2014; to date, Radiancy, has not been served. all plaintiffs.

The Company has filed a motionintends to dismiss this case; that motion is pending before the Court. A mediation was scheduled in this matter for November 24, 2014, but no settlement was reached. Radiancy and its officers intend todefend itself vigorously defend themselves against this lawsuit.suit. At this time, the amount of any loss, or range of loss, cannot be reasonably estimated as the case has only been initiated and no discovery has been conducted to determine the validity of any claim or claims made by plaintiffs. Therefore, the Company has not recorded any reserve or contingent liability related to these particular legal matters. However, in the future, as the cases progress, the Company may be required to record a contingent liability or reserve for these matters.

DSKX

On February 19, 2016, the Company and its subsidiaries entered into Agreements and Plans of Merger and Reorganization with DS Healthcare Group, Inc. and its subsidiaries (“DSKX”), under which DSKX would acquire the Company’s subsidiaries Radiancy, Inc. and PhotoMedex Technology, Inc. in exchange for shares of stock in DSKX as well as cash payments and notes for future cash payments. Subsequent to the signing of those Agreements, on March 23, 2016, after discussion with its independent registered public accounting firm, DSKX concluded that the unaudited condensed consolidated financial statements of DSKX for the two fiscal quarters ended June 30, 2015 and September 30, 2015 should no longer be relied upon because of certain errors in such financial statements. Also, DSKX reported that its audit committee, consisting of all members of its board of directors other than Daniel Khesin (at the time DSKX’s President and Chairman of the Board and a member of its board of directors), had engaged independent counsel to conduct an investigation regarding certain transactions involving Mr. Khesin and other individuals; the committee’s investigation had begun earlier in February. The board also reported that it had terminated the employment of Mr. Khesin as DSKX’s president and as an employee of DSKX, and also terminated Mr. Khesin’s employment agreement, dated December 16, 2013, for cause. 

The Company was not advised of this investigation during its negotiations with DSKX or after signing the Merger Agreements until the evening of March 21, 2016. On April 12, 2016, the Company sent a Reservation of Rights letter to DSKX. The Notice states that, based upon the disclosures set forth in DSKX’s Current Report on Form 8-K filed on March 23, 2016 and subsequent press releases and filings by DSKX with the United States Securities and Exchange Commission (collectively, the “DSKX Public Disclosure”), DSKX is in material breach of various representations, warranties, covenants and agreements set forth in the Agreements; had failed to provide to the Company the information contained in the DSKX Public Disclosures during the discussions relating to the negotiation and execution of the Agreements; and continues to be in material breach under the Agreements. As a result, the conditions precedent to the closing of these transactions as set forth in the Agreements may not be able to occur. The Notice also declares that the Company reserves all its rights and remedies under the Agreements, including, without limitation, the right to terminate the Agreements and collect a termination fee from DSKX of $3 million. The Notice further asserts that the Company regards certain provisions of the Agreements to have been waived by DSKX and to no longer be in effect, including the non-solicitation and no-shop provisions, negative covenants, and termination events, as applicable solely to the PHMD Group, as well as the payment of any termination fee by PHMD to DSKX. Finally, the Notice provided that the Company has the right to terminate the Agreements to pursue, consider and enter into any acquisition proposal or other transaction without the payment of fees and expenses to DSKX. 

On May 27, 2016, the Company and its subsidiaries Radiancy, Inc., an indirectly wholly-owned subsidiary of the Company (“Radiancy”), and PhotoMedex Technology, Inc., a wholly-owned subsidiary of the Company (“P-Tech”), terminated: (a) the Agreement and Plan of Merger and Reorganization, dated as of February 19, 2016 (the “Radiancy Merger Agreement”), among the Company, Radiancy, DS Healthcare Group, Inc. (“DSKX”) and PHMD Consumer Acquisition Corp., a wholly-owned subsidiary of DSKX (“Merger Sub A”), and (b) the Agreement and Plan of Merger and Reorganization, dated as of February 19, 2016 (the “P-Tech Merger Agreement” and together with the Radiancy Merger Agreement, the “Merger Agreements”), among the Company, P-Tech, DSKX, and PHMD Professional Acquisition Corp., a wholly-owned subsidiary of DSKX (“Merger Sub B”). Pursuant to the Merger Agreements, Radiancy was to merge with Merger Sub A, with Radiancy as the surviving corporation in such merger, P-Tech was to merge with Merger Sub B, with P-Tech as the surviving corporation in such merger, and DSKX was to become the holding company for Radiancy and P-Tech. 


Given the material breaches identified in the Company’s notice to DSKX, and other disclosures and communications by DSKX, in connection with the Company’s termination of the Merger Agreements and pursuant to their terms, the Company sought to recover a termination fee of $3.0 million, an expense reimbursement of up to $750, and its liabilities and damages suffered as a result of DSKX’s failures and breaches in connection with each of the Merger Agreements. On May 27, 2016, the Company, Radiancy and P-Tech filed a complaint in the U.S. District Court for the Southern District of New York alleging breaches of the Merger Agreements by DSKX and seeking the damages described in the foregoing sentence. On August 1, 2016, DSKX filed its answer to the complaint, denying the allegations stated in the complaint and alleging its own counterclaims including, among others, the Company’s alleged failure to disclose the Mouzon and Cantley cases filed against Radiancy.

On June 30, 2014,23, 2017, the Company'sCompany and its subsidiaries, Radiancy, Inc. (“Radiancy”) and PhotoMedex Technology, Inc. (“P-Tech”), entered into a Confidential Settlement and Mutual Release Agreement (the “DS Settlement Agreement”) with DS Healthcare Group, Inc. (“DSKX”) and its subsidiaries, PHMD Consumer Acquisition Corp. and PHMD Professional Acquisition Corp.

The terms of the DS Settlement Agreement are confidential. According to the DS Settlement Agreement the parties dismissed the suit between them with prejudice on June 23, 2017. The amount under this settlement agreement was recorded under discontinued operation.

Linda Andrews

During 2016, Linda Andrews, an alleged user of the no!no! Hair device, filed a product liability claim against the Company, its subsidiary Radiancy, Inc., was served with a class action lawsuit filedand Dr. Dolev Rafaeli, in the SuperiorUnited States District Court infor the StateMiddle District of California, County of Kern. The suit was filed by April Cantley, who purchased Radiancy's no!no! Hair products. It alleges various violations of state business and consumer protection codes including false and misleading advertising, breach of express and implied warranties and breachFlorida, Orlando Division, alleging that use of the California Legal Remedies Act.device had caused a relapse of and complication to a pre-existing medical condition resulting from her treatment for cancer. The complaint seeks certificationalleged, among other claims, that Radiancy failed to provide adequate warnings regarding the operation of the class, which consists of customers indevice. The Company and Dr. Rafaeli filed a motion to dismiss the State of California who purchased the no!no! Hair devices. The complaint also seeks an unspecified amount of monetary damages, pre-and post-judgment interest and attorneys' fees, expert witness fees and other costs.claims against them; Radiancy has filed an Answeranswer to this Complaint;the Complaint. Ms. Doe then sought leave to amend her complaint to clarify the claims; the Company, Radiancy and Dr. Rafaeli filed appropriate responses and renewed the motion to dismiss the claims against the Company and Dr. Rafaeli. 

On June 22, 2017, the United States District Court for the Middle District of Florida, Orlando Division, dismissed the Company and Dr. Dolev Rafaeli, its former Chief Executive Officer, from the case is now in the discovery phase.of Linda Andrew v. Radiancy, and its officers intend to vigorously defend themselves against this lawsuit. Discovery has now commenced in this action. At this time, the amount of any loss, or range of loss, cannot be reasonably estimated as the case has only been initiated and no discovery has been conducted to determine the validity of any claim or claims made by plaintiffs. Therefore,Inc.; the Company has not recorded any reserve or contingent(under the name PhotoMedex, Inc.); and Dr. Rafaeli. Ms. Andrew had filed a product liability related to these particular legal matters. However, in the future, as the cases progress,suit alleging damages from her use of a no!no! hair device. The claims against the Company may be required to recordand Dr. Rafaeli were dismissed without prejudice. The Company’s subsidiary, Radiancy, Inc., entered into a contingentsettlement with Ms. Andrews in 2017; the terms of the settlement are confidential.

Other litigation

The Company and certain subsidiaries are, and have been, involved in other miscellaneous litigation and legal actions, including product liability, or reserve for these matters.

Fromconsumer, commercial, tax and governmental matters, which can arise from time to time in the ordinary course of our business, we and certain of our subsidiaries are involved in certain other legal actions and claims, including product liability, consumer, commercial, tax and governmental matters, and claims regarding false advertising and product efficacy against the no!no! Hair products which were already raised and reviewed in the Tria litigation. We believe, based on discussions with legal counsel,business. The Company believes that these other litigations and claims will likely be resolved without a material effect on our consolidated financial position, results of operations or liquidity. However, litigation isand legal actions are inherently unpredictable, and excessive verdicts can result from litigation.in such situations. Although we believe wethe Company believes it has or will have substantial defenses in these matters, weit may, in the future, incur judgments or enter into settlements of claims that could have a material adverse effect on our results of operations in a particular period.
F-29


Employment Agreements

Avalon

On January 12, 2018, we received a copy of a complaint, dated November 17, 2017, that was filed by Alpha Alpha, LLC in the Thirteenth Judicial District Court in the County of Valencia in the State of New Mexico against Avalon Jubilee, LLC, the holding company that owns the property in Los Lunas, New Mexico, HiTex, LLC, MCBB, LLC, Land Strategies, LLC, Ronald R. Cobb and John Does 1–5. The suit asks the court to, among other things, determine whether there have been unauthorized transfers of interest in Avalon Jubilee LLC; and declare who are the holders of interests in Avalon Jubilee LLC. Although the complaint does not name the Company or any of its subsidiaries or specifically question the Company’s interest in Avalon Jubilee LLC, it raises questions about whether the transfers of interest leading to our acquisition of our interest in Avalon Jubilee LLC (under the Contribution Agreement described in Note 5) were properly made in accordance with the Avalon Jubilee operating agreement. The Company has severance agreementsbegun an internal investigation into this matter and will disclose the results of that investigation once it has been completed. Although neither our company nor any of its subsidiaries is a party to litigation regarding this matter, we recognized an impairment expense of $862 to account for our estimate of the impact that such litigation may have on the operations and fair value of the underlying asset.


Registration Rights Agreement with certain key executivesParty to the Purchase Agreement

As discussed in Note 14, as a condition to the first closing under the Purchase Agreement, the Company entered into a registration rights agreement (the “Registration Rights Agreement”) with the Investor, pursuant to which the Company agreed to register all shares of Common Stock that may be issued upon conversion of the Series B Preferred Stock (the “Registrable Securities”) under the Securities Act of 1933, as amended (the “Securities Act”). The Company agreed to file a registration statement covering the resale of such Registrable Securities within 30 days of the first closing and employeescause such registration statement to be declared effective under the Securities Act as soon as possible but, in any event, no later than 120 days following the filing date if such registration statement is filed on Form S-3 or 150 days if such registration statement is filed on Form S-1. If such registration statement is not filed or declared effective by the Securities and Exchange Commission on or prior to such dates, or if after such registration statement is declared effective, without regard for the reason thereunder or efforts therefor, such registration statement ceases for any reason to be effective for more than an aggregate of 30 trading days during any 12-month period, which need not be consecutive, then in addition to any other rights the holders of Series B Preferred Stock may have under the Registration Rights Agreement or under applicable law, the Company shall pay to each holder an amount in cash, as partial liquidated damages and not as a penalty, equal to 1% of the product obtained by multiplying (x) the Series B Original Issue Price by (y) the number of shares of Registrable Securities held by the holder (such product being the “Investment Amount”); provided that, create certain liabilitiesin no event will the Company be liable for liquidated damages in excess of 1% of the Investment Amount in any single month and that the maximum aggregate liquidated damages payable to the holders under the Registration Rights Agreement shall be 10% of the Investment Amount. On January 23, 2018, the Company filed a registration statement on Form S-3 to register the shares issued to OFI in the first closing. OFI waived its right to liquidated damages in connection with the late filing of such registration statement. 

Registration Rights Agreements with Payout Note Holders

As discussed in Note 14, the Payout Notes were convertible into shares of common stock and the Company agreed to register the shares underlying the Payout Notes within thirty (30) days of issuance with best efforts to cause the registration statement covering such shares to become effective within one-hundred twenty (120) days of issuance. On November 14, 2017, the Company filed a registration statement on Form S-3 (the “First Registration Statement”) to register all shares that may be issued upon conversion of the Payout Notes, which was subsequently amended to include the Payout Shares issued under the Stock Grant Agreement. In connection with the Stock Grant Agreement, the Company entered into a registration rights agreement (the “Payout Registration Rights Agreement”) with the Note Holders, pursuant to which the Company agreed to register the shares of common stock under the Additional Shares under the Securities Act. The Company agreed to file a registration statement covering the resale of the Additional Shares within 30 days of the Stock Grant Agreement and cause such registration statement to be declared effective under the Securities Act as soon as possible but, in any event, of their termination of employmentno later than 120 days following the filing date if such registration statement is filed on Form S-3 or 150 days if such registration statement is filed on Form S-1. If such registration statement is not filed or declared effective by the companySecurities and Exchange Commission on or prior to such dates, or if after such registration statement is declared effective, without cause,regard for the reason thereunder or followingefforts therefor, such registration statement ceases for any reason to be effective for more than an aggregate of 30 trading days during any 12-month period, which need not be consecutive, then in addition to any other rights the Note Holders may have under the Payout Registration Rights Agreement or under applicable law, the Company shall pay to each Note Holder an amount in cash, as partial liquidated damages and not as a change in controlpenalty, equal to 1% of the Company.product obtained by multiplying (x) $1.00 by (y) the number of shares of Common Stock held by the Note Holder included in the registration statement (such product being the “Payout Investment Amount”); provided that, in no event will the Company be liable for liquidated damages in excess of 1% of the Payout Investment Amount in any single month and that the maximum aggregate liquidated damages payable to the Note Holders under the Payout Registration Rights Agreement shall be 10% of the Payout Investment Amount. The aggregate commitment under these executive severance agreements, shouldregistration rights provision contained in the Payout Notes was incorporated by reference into the Payout Registration Rights Agreement, except that the Note Holders waived the breach by the Company for failure to timely file the First Registration Statement and agreed that they are not entitled to liquidated damages as a result of such failure. Under the Payout Registration Rights Agreement, the Note Holders are entitled to liquidated damages if the First Registration Statement is not declared effective within 120 days following the date of the Payout Notes, but the Note Holders subsequently agreed to waive their rights to such liquidated damages until April 20, 2018. On January 23, 2018, the Company filed a registration statement on Form S-3 for the Additional Shares. The Note Holders waived their rights to liquidated damages in connection with the late filing of such registration statement and in connection with the effectiveness deadline for such registration statement until April 20, 2018.


Note 14

Stockholders’ Equity:

Common Stock

The Company’s common stock confer upon their holders the following rights: 

The right to participate and vote in the Company’s stockholder meetings, whether annual or special. Each share will entitle its holder, when attending and participating in the voting in person or via agent or letter, to one vote;

The right to a share in the distribution of dividends, whether in cash or in the form of bonus shares, the distribution of assets or any other distribution pro rata to the par value of the shares held by them;

The right to a share in the distribution of the Company’s excess assets upon liquidation pro rata to the par value of the shares held by them.

Convertible Series A Preferred Stock

The terms of the Convertible Series A Preferred Stock are governed by a certificate of designation, or the Series A Certificate of Designation, filed by the Company with the Nevada Secretary of State on May 15, 2017. Pursuant to the Series A Certificate of Designation, the Company designated 3,000,000 shares of the Company’s preferred stock as Series A Convertible Preferred Stock. As more fully described in Note 5, the Company issued 123,668 share of Convertible Series A Preferred Stock in connection with the Contribution Agreement. Following is a summary of the material terms of the Series A Convertible Preferred Stock: 

Liquidation -Upon any liquidation, dissolution or winding-up of the Company, whether voluntary or involuntary, the holders shall be entitled to receive out of the assets, whether capital or surplus, of the Corporation, after the Redeemable Convertible Series B Preferred Stockholder’s liquidation preference, the same amount that a holder of Common Stock would receive if the Convertible Series A Preferred Stock were fully converted (disregarding for such purposes any conversion limitations hereunder) to Common Stock which amounts shall be paid pari passu with all holders of Common Stock.

Voting -Except as otherwise provided in the Series A Certificate of Designation or as otherwise required by law, the Convertible Series A Preferred Stock shall have no voting rights. However, as long as any shares of Convertible Series A Preferred Stock are outstanding, we shall not, without the affirmative vote of the holders of a majority of the then outstanding shares of the Convertible Series A Preferred Stock, (a) alter or change adversely the powers, preferences or rights given to the Convertible Series A Preferred Stock or alter or amend the Series A Certificate of Designation, (b) amend the Company’s articles of incorporation or other charter documents in any manner that adversely affects any rights of the holders, (c) increase the number of authorized shares of Convertible Series A Preferred Stock, or (d) enter into any agreement with respect to any of the foregoing.


Conversion - Each share of Convertible Series A Preferred Stock shall be convertible, at any time and from time to time from at the option of the holder thereof, into that number of shares of common stock determined by dividing $62.9575 by the Conversion Price. The Conversion Price for the Series A Convertible Preferred Stock is equal to $2.5183, subject to adjustment as described in the Series A Certificate of Designation.

Dividends- Except for stock dividends or distributions for which adjustments are to be made, holders shall be entitled to receive, and the Company shall pay, dividends on shares of Convertible Series A Preferred Stock equal (on an as-if-converted-to-Common-Stock basis) to and in the same form as dividends actually paid on shares of the Common Stock when, as and if such dividends are paid on shares of the Common Stock. No other dividends shall be paid on shares of Convertible Series A Preferred Stock.

Redeemable Convertible Series B Preferred Stock

Convertible Series B preferred stock confer upon their holders all covered executivesthe rights of Common Stock. As more fully described below, the Company issued 1,500,000 shares of Redeemable Convertible series B Preferred Stock in connection with the Securities Purchase Agreement. In addition, based on the Company’s Certificate of Designation, the Series B Shares bear the following rights and employees be terminated other than for cause, was approximately $10,073privileges:

Liquidation Preference -Holders of the Series B Shares shall receive cumulative dividends, pro rata among such holders, prior to and in preference to any dividend on the Company’s outstanding Common Stock and Series A Convertible Preferred Stock, at the per annum rate of 8% of the Series B Original Issue Price ($1.00). Dividends on each Series B Share will accrue daily and be cumulative from the original issued date of December 22, 2017 and shall be payable upon the occurrence of any voluntary or involuntary liquidation, dissolution or winding up of the, a conversion or a redemption. The redemption price shall be $1.00 per share, subject to appropriate adjustment. Holders shall also be entitled to receive dividends on the Series B Shares (on an as-if-converted-to-Common-Stock basis) as dividends actually paid on shares of the Company’s Common Stock when, as and if such dividends are paid on shares of the Common Stock.

As of December 31, 2014, based on 2014 salary levels. Should all covered executives and certain key employees be terminated following a change in control of the Company,2017, the aggregate commitment under these executive severance agreements at December 31, 2014 was approximately $9,820, based on 2014 salary levels.

Note 12
Stockholders' Equity:
Preferred Stock
liquidation preference amounted to $1,503. The Company has authorized preferred stock consisting of 5,000,000 shares with a $.01 par value, which shall be designatedforegoing dollar amount does not include dividends, as blank check preferred. Thethe Company’s Board of Directors may authorizehas not declared any dividends since inception.

Voting -Each holder of the Series B Shares shall be entitled to cast the number of votes equal to the number of whole shares of Common Stock into which the shares of Series B Shares held by such holder are convertible as of the record date for determining stockholders entitled to vote on such matter subject to certain conversion limitations.

Conversion -Each Series B Share shall be convertible at the option of the holder thereof, at any time after the date of issuance of such share, into such number of fully paid and non-assessable Common Stock as is determined by dividing the original issue price plus accrued, but unpaid, dividends by the applicable conversion price at that time in effect for such Series B Share. The Series B Shares are automatically converted to Common Stock on May 31, 2018 should voluntary conversion or redemption not occur prior to that time.

Redemption – Under certain conditions beyond the Company’s control, the Series B shareholders may require redemption of the Series B Shares at a price per share equal to $1.33, plus accrued, but unpaid, dividends through and including the date of such redemption.

Reverse Split and Retroactive Adjustment of Shares and Per Share Information

On September 7, 2016, the issuance from time to time of one or more classes of preferred stock with one or more series within any class thereof, with such voting powers, full or limited, or without voting powers and with such designations, preferences and relative, participating, optional or special rights and qualifications, limitations or restrictions thereon as shall be set forth in the resolution or resolutions adopted by the Board of Directors providing for the issuance of such preferred shares. At December 31, 2014 and 2013, no shares of preferred stock were issued or outstanding.

Common Stock
On December 12, 2014, the Company closed on a registered offering in which it sold an aggregate of 645,000 shares of its common stock at an offering price of $2.19 per share. The closing price of the Company's common stock was $1.37 on December 12, 2014. The sale resulted in net proceeds of approximately $1.4 million.
On August 18, 2012, theCompany’s Board of Directors approved a reverse stock repurchase programsplit in a ratio of 1-for-5 (the “2016 Reverse Split”). The amount of authorized Common Stock as well as the par value for the Common Stock were not effected. Any fractional shares resulting from the 2016 Reverse Split were rounded up to the nearest whole share. 

All common stock, stock warrants, stock options and per share amounts set forth herein are presented to give retroactive effect to the 2016 Reverse Split for all periods presented.

Change of Authorized Shares

On October 19, 2017, the Company filed Amended and Restated Articles of Incorporation to among the other things, increase in the number of authorized shares of common stock, $.01 par value per share, of the Company from 50,000,000 shares to 500,000,000 million shares and increase the number of authorized shares of preferred stock, $.01 par value per share, of the Company from 5,000,000 shares to 50,000,000 shares.


Contribution Agreement

As discussed in Note 5, upon the Initial Closing of the First Contribution, the Company issued to the Contributor 879,234 duly authorized, fully paid and non-assessable shares of the Company’s common stock, par value $0.01 per share and 123,668 shares of the Company’s newly designated non-voting Series A Convertible Preferred Stock, par value $0.01 per share for certain Contributed Properties.

Payout Notes

Following the Initial Closing of the First Contribution under the Contribution Agreement (see also Note 5), amounts due to Dr. Dolev Rafaeli, the Company’s former Chief Executive Officer and Dennis McGrath, the Company’s former Chief Financial Officer under their employment agreements, as well as amounts due to Dr. Yoav Ben-Dror for his services as a maximumboard member of $25 million.the Company’s foreign subsidiaries, were to be converted to convertible secured notes (the “Payout Notes”) after approval from the Company’s stockholders. The Payout Notes would be due one year after the stockholder approval and carry a 10% interest rate. The principal would convert to shares of the Company’s Common Stock at the lower of (i) the Per Share Value or (ii) the VWAP with respect to on-exchange transactions in the Company’s Common Stock executed on the NASDAQ during the 30 trading days prior to the maturity date as reported by Bloomberg L.P.; provided, however, that the value of the Company’s Common Stock should in no event be less than $1.75 per share. The Payout Notes would be secured by a security interest in all assets of the Company; provided, however, that such security interest would be subordinated to any (i) claims or liens to the holders of any debt (including mortgage debt) being assumed by the Company as a result of the transaction contemplated by the Agreement, and (ii) all post-closing indebtedness incurred by the Company or its subsidiaries. The holders of the Payout Notes would have registration rights which would require the filing of a re-sale registration statement on appropriate form that registers for re-sale the shares of Common Stock underlying the Payout Notes within thirty (30) days of issuance with best efforts to cause the same to become effective within 120 days of issuance. The form of those Payout Notes was agreed to at the time of signing of the Contribution Agreement and was attached as an exhibit thereto. In August 2013,connection with the Payout Notes, the parties also agreed to a form of security agreement (the “Security Agreement”), which was also attached as an exhibit to the Contribution Agreement. 

On October 12, 2017, following approval by the Company’s stockholders, the Company issued a secured convertible promissory notes (the “Payout Notes”) to Dr. Dolev Rafaeli, the Company’s former Chief Executive Officer, Dennis M. McGrath, the Company’s former President and Chief Financial Officer, and Dr. Yoav Ben-Dror, the former director of the Company’s foreign subsidiaries (collectively, the “Note Holders”) in the principal amounts of $3,134, $978 and $1,515, respectively. The Payout Notes were due on October 12, 2018, carried a 10% interest rate, payable monthly in arrears commencing on December 1, 2017 (each such payment, a “Monthly Interest Payment” and each date of such payment, an “Interest Payment Date”), and were convertible into shares of the Company’s Common Stock at maturity. The Payout Notes were secured by a security interest in all of the properties, assets and personal property of the Company (the “Security Agreement”). 

On December 22, 2017, the Company and the Note Holders entered into a stock grant agreement (the “Stock Grant Agreement”) to cause the early conversion of the Payout Notes into an aggregate of 5,628,291 shares of the Company’s Common Stock (the “Payout Shares”), valued at $5,626 based on the quoted share price in the market for our common stock on December 22, 2017, and to effectuate the release of all security interests associated with the Payout Notes.

Pursuant to the Stock Grant Agreement, the Company also agreed to provide for the issuance of an aggregate of 1,857,336 additional shares of Common Stock to the Note Holders as consideration for the various agreements of the Note Holders contained in the Stock Grant Agreement (the “Additional Shares”), subject to stockholder approval. In addition, as promptly as possible following entry into the Stock Grant Agreement, the Company is required to file a proxy statement and hold a special meeting of its stockholders to authorize and approve the issuance of the Additional Shares. As of December 31, 2017, a proxy statement was not filed, and special meeting of the stockholders has not been held. Therefore, during the year ended December 31, 2017, no expenses have been recorded in connection with the Additional Shares.

Pursuant to the Stock Grant Agreement, the Company also agreed to make 12 monthly payments on the first of each month commencing on January 1, 2018 in the amounts of $21, $7 and $10 to Messrs. Rafaeli, McGrath, and Ben-Dror, respectively (collectively, the “Cash Payments”). The Cash Payments equal to the interest payments that would have been made to the Note Holders absent the conversion of the Payout Notes and are consideration for certain consulting services provided by the Note Holders specified in the Stock Grant Agreement. 


In addition, Dr. Dolev Rafaeli and Dennis M. McGrath resigned from the Board of Directors has authorized an additional $30 million share re-purchase program of its common sharesthe Company effective upon the last to occur of (i) receipt of all of the Payout Shares and all of the Additional Shares, (ii) receipt of all of the Cash Payments (either in accordance with the schedule provided in the open market overStock Grant Agreement or, at the next twelve months, at such timesCompany’s option, in one lump sum on an accelerated basis), and prices as determined appropriate by(ii) the Company's managementdate that the Payout Shares and the Additional Shares have been registered for re-sale in collaborationaccordance with the BoardPayout Registration Rights Agreement. 

In connection with the Stock Grant Agreement, the Security Agreement was automatically terminated. 

Shares to former Chief Executive Officer

On December 22, 2017, Mr. Suneet Singal resigned from his position as Chief Executive Officer of Directors. To date,the Company, effective as of January 2, 2018. In connection with such resignation, on December 22, 2017, the Company and Mr. Singal entered into a separation agreement (the “Agreement”), pursuant to which Mr. Singal agreed to resign and the Company agreed to issue to Mr. Singal 1,000,000 shares of the Company’s Common Stock, 333,333 shares of which will vest immediately, 333,333 shares of which will vest upon the first anniversary of the Agreement, and 333,334 shares of which will vest upon the second anniversary of the Agreement. 

Since the aforesaid shares of common stock were agreed to have been granted to Mr. Singal as a result of his resignation from the Chief Executive Officer position and Mr. Singal has no obligation to render service in the future with respect to the additional Shares, the Company has repurchased 2,987,413recognized an amount of $910 as part of the general and administrative expenses in the consolidated statement of comprehensive loss. The amount was determined based on the quoted share price in the market as of the December 22, 2017.

Securities Purchase Agreement

On December 22, 2017, the Company entered into a Securities Purchase Agreement (the “Purchase Agreement”) with Opportunity Fund I-SS, LLC, a Delaware limited liability company (the “Investor”), under which the Investor may, but is not obligated to, invest up to $15 million in the Company in a series of closings over a period prior to December 31, 2018, in exchange for which the Investor will receive shares of the Company’s newly designated Redeemable Convertible Series B Preferred Stock (“Series B Shares) at a purchase price of $1.00 per share (the “Option”). 

On December 22, 2017 (the “Initial Date”), the Company and the Investor completed the first closing under the Purchase Agreement, pursuant to which the Investor exercised a portion of the Option and provided $1,500 to the Company in exchange for 1,500,000 shares of Series B Shares.

Proceeds from any subsequent closings must be used to invest in Income Generating Properties (as that term is defined in the Purchase Agreement) that have been approved by the Company’s Board of Directors or as otherwise agreed to between the Company and the Investor in writing prior to such subsequent closings. 

Under ASC 480, “Distinguishing Liabilities from Equity” preferred stock that is not redeemable or is redeemable solely at the option of the issuer shall be included in stockholders’ equity. If the instrument meets any of the following criteria, mezzanine classification between liabilities and stockholders’ equity would be required: 

it is redeemable at a fixed or determinable price on a fixed or determinable date or dates

it is redeemable at the option of the holder; or

It has conditions for redemption which are not solely within the control of the issuer, such as stocks which must be redeemed out of future earnings

In addition, per ASC 480, deemed liquidation events that require (or permit at the holders options) the redemption of only one or more of a particular class of equity instrument for cash or other assets cause those instruments to be considered contingently redeemable and therefore, subject to mezzanine classification. 

Since the Series B Shares have conditional redemption provisions which are outside of the control of the Company and also contain a deemed liquidation preference, the Series B Shares were classified as mezzanine financing at their initial fair value at the Initial Date. Subsequent measurement is unnecessary if it is not probable that the instrument will become redeemable. If it is probable that the equity instrument will become redeemable the following measurement methods shall be applied in accordance with either of the following methods and shall be applied in a consistent manner:

Accrete changes in the redemption value over the period from the date of issuance (or from the date that it becomes probable that the instrument will become redeemable, if later) to the earliest redemption date of the instrument using an appropriate methodology, usually the interest method. Changes in the redemption value are considered to be changes in accounting estimates.


Recognize changes in the redemption value (for example, fair value) immediately as they occur and adjust the carrying amount of the instrument to equal the redemption value at the end of each reporting period. This method would view the end of the reporting period as if it were also the redemption date for the instrument.

Under ASC 480, the aforementioned written call Option is considered freestanding, as the Company believes it is legally detachable and separately exercisable. As the option is exercisable for shares subject to possible redemption at the option of the holder, as of the Initial Date, the Option was measured at fair value in total amount of $5,584 and recorded as a non-current financial liability on the consolidated balance sheet as of December 31, 2017. Excess of the initial value of the option liability over the proceeds received, amounting to $4,084, was charged immediately into the consolidated statement of comprehensive loss as financing expenses. As such, there were no residual proceeds to allocate to the Series B preferred shares at an average pricethe Initial Date.

The Option is marked to market in each reporting period when changes in the fair value of $13.98 per share for a totalthe Option are charged into statement of $41,757.

On April 27, 2012,comprehensive loss. Consequently, during the year ended December 31, 2017, the Company closed on a two-tranche registered offeringrecorded finance income of $1,194 related to change in the fair value of the instrument during the period from the Initial Date through December 31, 2017.

In addition, the Company has incurred direct and incremental issuance costs amounting to $42 which it sold an aggregatewere charged immediately into the consolidated statement of 3,023,432comprehensive loss as finance expenses, as the Option was presented at fair value at the Initial Date.

On December 22, 2017, each Series B Share was convertible into 1.24789 shares of its common stock valued at an offering price of $13.23$1.00 per share. The sale resulted in net proceedsAs a result, Beneficial Conversion Feature (the “BCF”) amounting to approximately $372 was measured assuming full conversion. However, the conversion of approximately $37.8 million. The netthe Preferred Stock is subject to certain contingencies, which impact the timing and amount of the BCF. As of December 31, 2017, the Company should record a BCF for the Preferred Stock for any shares convertible at that time without requiring stockholder approval through the planned proxy statement. However, as no residual proceeds were usedallocable to the Series B Shares, no BCF was recognized at December 31, 2017. 

The fair value of the Option was based on management estimates and values derived from a calculation to provide an approximate indication of value. The fair value of Option was estimated at the Initial Date and December 31, 2017 by using hybrid method that includes scenario of conversion and scenario liquidation and the Black-Scholes option pricing model. In the first scenario, the Series B Preferred Stock price applied in the model was assumed based on the as-converted price on the date of estimation. Expected volatility was estimated by using a group of peers in the real estate development, homebuilding and income-producing properties sectors, and applying a 75% percentile ranking based on the total capitalization of the Company. In the second scenario, the option was estimated based on the value of the option in a proposed liquidation scenario. A probability weighting was applied to determine the expected value of the option. 

The following are the key underlying assumptions that were used:

Option Value:

  December 22,
2017
  December 31,
2017
 
Dividend yield (%)  0   0 
Expected volatility (%)  36.9   36.9 
Risk free interest rate (%)  1.72   1.74 
Strike price  1.00   1.00 
Series B Preferred Stock price  1.24   1.13 
Probability of if-converted scenario (%)  90   90 
Probability assumed liquidation scenario (%)  10   10 
Expected term of Option (years)  1.0   1.0 

In the absence of voluntary conversion and assuming no breaches as described above under “Redemption”, the Series B Shares automatically convert on May 31, 2018. As such, accretion adjustments to the carrying amount of the Series B Shares to the automatic conversion date of May 31, 2018 are recorded as deemed dividends. 


The table below summarizes the change in the mezzanine financing during the year ended December 31, 2017: 

  

December 31, 

2017 

 
    
Opening balance $ 
Proceeds from issuance of Series B Shares  1,500 
Recognition of written call Option as a discount of Series B Shares  (1,500)
Amortization of discount  84 
Accretion of cumulative dividend  3 
     
Closing balance $87 

In addition, upon the Purchase Agreement, the Company agreed the following:

To nominate two directors to the Company’s Board of Directors upon request of the Investor (see also Note 17).

So long as the shares of Series B Shares purchased by the Investor are outstanding, the Company’s debt (as defined by U.S. generally accepted accounting principles) shall not exceed 45% of its fixed assets without the prior written consent of the Requisite Holders. As of December 31, 2017, the covenant has been met by the Company.

Subject to stockholder approval, to amend the Certificate of Designation for the Company’s Series A Shares to change the conversion price from $2.5183 to $1.12024 such that each share of Series A Share will be initially convertible into 56.2 shares of Common Stock instead of 25 shares of Common Stock.

The above inducement is considered as modification for general corporate purposes, including capital expenditures, continued product development, sales and marketing initiatives and working capital.

which the fair value of the Series A Shares shall be measured pre-and post-modification subject to the stockholders’ approval. Should the fair value change by greater than 10% as a result of the modification, any original Series A Shares will be considered extinguished with the incremental value reflected in expense. Should the modification not result in a greater than 10% change, the modification of the conversion feature for the Series A Shares will be treated analogous to modification for stock compensation arrangements. Any incremental value, will be recorded as a deemed dividend to the Series A Shareholders.

As of December 31, 2017, the stockholders’ approval has not been taken place.

Common Stock Options

The Company has a Non-Employee Director Stock Option Plan. This plan has authorized 370,00074,000 shares; of which 7,0002,135 shares had been issued or were reserved for issuance as awards of shares of common stock, and 14,57812,079 shares were reserved for outstanding stock options. The directors, who were electedAs of December 31, 2017 the number of shares available for future issuance pursuant to our Board in connection with the reverse merger, each received a one-time stock award of 5,000 shares of the Company's common stock in January 2012.

this plan is 71,865.

In addition, the Company has a 2005 Equity Compensation Plan ("(“2005 Equity Plan"Plan”). The 2005 Equity Plan which has authorized 6,000,0001,200,000 shares, of which 1,576,095467,328 shares had been issued or were reserved for issuance as awards of shares of common stock, and 1,144,976143,815 shares were reserved for outstanding options.

F-30


There are no further shares available for future issuance pursuant to this plan.

A summary of stock option transactions for all ofunder the Company's stock optionsNon-Employee Director Stock Option Plan and the 2005 Equity Plan during the years ended December 31, 2014, 20132017 and 2012 follows:

 Number of Stock OptionsWeighted Average Exercise Price
Outstanding at December 31, 2011180,718$ 19.54
Granted739,00015.87
Exercised(10,048)6.67
Expired/cancelled(11,129)20.25
Outstanding at December 31, 2012898,54116.65
Granted259,62516.59
Exercised(3,750)6.24
Expired/cancelled(21,738)31.36
Outstanding at December 31, 20131,132,67816.51
Granted181,50014.10
Exercised--
Expired/cancelled(154,624)15.73
Outstanding at December 31, 20141,159,554$16.23
Exercisable at December 31, 2014510,954$16.47
The outstanding and exercisable options at December 31, 2014, have a range of exercise prices and associated weighted remaining contractual life and weighted average exercise price,2016 were as follows:

   Number of Stock Options  Weighted Average Exercise Price 
Outstanding at December 31, 2015   150,138   67.99 
Granted       
Exercised       
Expired/cancelled   (15,988)  82.26 
Outstanding at December 31, 2016   134,150  $85.22 
Granted       
Exercised       
Expired/cancelled   (133,150)  91.43 
Outstanding at December 31, 2017   1,000  $75.00 
Exercisable at December 31, 2017   800  $75.00 



 
Options Range of Exercise Prices
 
Outstanding Number of Shares
Weighted Average Remaining Contractual Life (years)
 
Weighted Average Exercise Price
 
Exercisable Number of Shares
 
Exercisable Weighted Avg. Exercise Price
$0      - $7.5021,5844.58$   6.1221,584$   6.11
$7.51 - $15.00699,6227.85$   14.11255,022$   13.93
$15.01 - $22.50427,9007.32$   19.02223,900$   18.13
$22.51- up10,4481.56$   64.4210,448$   64.42
Total1,159,5547.54$   16.23510,954$   16.47
The outstanding options will expire, as follows:
Year EndingNumber of SharesWeighted Average Exercise Price
 
 
Exercise Price
20152,499$102.90$102.90
20162,634$ 69.48$48.72 - $93.66
20173,146$ 46.85$46.62 - $47.88
20182,169$ 39.41$37.80 - $39.90
2019 and later1,149,106$ 15.79$5.70 - $20.00
 1,159,554$ 16.23$5.70 - $102.90
As the share price as

A summary of December 31, 2014 was $1.53, the aggregate intrinsic value for options outstanding and exercisable was immaterial.

F-31


The Company uses the Black-Scholes option-pricing model to estimate fair value of grants ofnon-vested restricted stock options with the following weighted average assumptions:
 Year Ended December 31,
 2014 2013 2012
Risk-free interest rate2.17% 1.3% N/A
Volatility78.41% 85.25% N/A
Expected dividend yield0% 0% N/A
Expected life5.5 years 5.5 years N/A
Estimated forfeiture rate0% 0% N/A
The Company calculates expected volatility for a share-based grant based on historic daily stock price observations of its common stock. For estimating the expected term of share-based grants made induring the years ended December 31, 20142017 and 2013, the Company has adopted the simplified method. 2016, were as follows:

   Shares of restricted stock  Weighted Average Grant-Date Fair Value 
Non-vested at December 31, 2015   258,572   10.57 
Granted       
Vested/cancelled   (129,211)  10.04 
Non-vested at December 31, 2016   129,361   11.11 
Granted       
Vested/cancelled   (122,861)  14.69 
Non-vested at December 31, 2017   6,500   9.25 

The Company has used historical data to estimate expected employee behaviorstotal equity-based compensation expense related to option exercises and forfeitures and included these expected forfeitures as a partall of the estimate of expense as of the grant date.

With respect to grants of options, the risk-free rate of interest is based on the U.S. zero-coupon US Government bond rates appropriate for the expected term of the grant or award.
On December 10, 2014, the Company issued 290,000 restricted stock units to a number of employees. The restricted shares have a purchase price of $0.01 per share and vest, and cease to be subject to the Company's right of repurchase, over a four-year period. The Company determined the fair value of theCompany’s equity-based awards, to be the fair value of the Company's common stock units on the date of issuance less the value paid for the award. The aggregate fair value of these restricted stock issued was $435. On November 7, 2014, the Company also issued 390,000 restricted stock units to two executive employees. The restricted shares have a purchase price of $0.01 per share and vest, and cease to be subject to the Company's right of repurchase, over a four-year period. The Company determined the fair value of the awards to be the quoted market value of the Company's common stock on the date of issuance less the value paid for the award. The aggregate fair value of these restricted stock issued was $1,217.
On May 12, 2014, the Company granted 141,337 restricted stock units to three LCA employees as part of their respective employment agreements related to the acquisition. These restricted shares have a purchase price of $0.01 per share and vest, and cease to be subject to the Company's right of repurchase, over a three-year period. The Company determined the fair value of the awards to be the quoted market value of the Company's common stock on the date of issuance less the value paid for the award. The aggregate fair value of these restricted stock issued was $1,936. The Company also granted an aggregate of 109,000 options to purchase common stock to a number of employees with a strike price of $13.70, which was higher than the quoted market value of our stock at the date of grants. The options vest over four years and expire ten years from the date of grant. The aggregate fair value of these options granted was $975.
On April 17, 2014, the Company issued 5,000 shares of common stock to a non-employee director for an aggregate fair value of $75.
On February 27, 2014, the Company granted an aggregate of 71,500 options to purchase common stock to a number of employees and consultants with a strike price of $14.80, which was higher than the quoted market value of our stock at the date of grants. The options vest over five years and expire ten years from the date of grant. The aggregate fair value of the options granted was $718.
F-32


On February 28, 2013, the Company granted an aggregate of 177,125 options to purchase common stock to a number of employees and consultants with a strike price of $15, which was higher than the quoted market value of our stock at the date of grants. The options vest over five years and expire ten years from the date of grant. Also on February 28, 2013, the Company granted an aggregate of 82,500 non-qualified options to purchase common stock to two executive employees with a strike price of $20, which was set to match the exercise price of the warrants issued in the reverse merger and was higher than the quoted market value of our stock at the date of grant. The aggregate fair value of the options granted was $2,590. The options vest over five years and expire ten years from the date of grant.
On January 26, 2012, the Company issued 30,000 shares of common stock to the six non-employee directors with an aggregate fair value of $405.
On March 18, 2012, the Company granted an aggregate of 509,000 options to purchase common stock to a number of employees and consultants with a strike price of $14, which was higher than the quoted market value of our stock at the date of grants. The options vest over five years and expire ten years from the date of grant. Also on March 18, 2012, the Company granted an aggregate of 230,000 non-qualified options to purchase common stock to two executive employees with a strike price of $20, which was set to match the exercise price of the warrants issued in the reverse merger and was higher than the quoted market value of our stock at the date of grant. The aggregate fair value of the options granted was $6,652. The options vest over five years and expire ten years from the date of grant.
Total stock-based compensation expense was as $4,936, $4,985 and $6,197 forrecognized during the years ended December 31, 2014, 20132017 and 2012.
2016, as part of the discontinuing operation in total amount of $69 and $1,969, respectively. In addition, during the years ended December 31, 2017, an amount of $2,364 was recorded as general and administrative expenses as part of continuing operation.

At December 31, 2014,2017, there was $7,644$35 of total unrecognized compensation cost related to non-vested stock awards that isbased on their original vesting terms was expected to be recognized over a weighted-average period of 3.14.17 years.

Common Stock Warrants
As a result Following the completion of the cash raisetransaction described in Note 17, such compensation will be accelerated.

F-39 

Note 15

Income Taxes:

On December 22, 2017, the U.S. government enacted comprehensive tax legislation commonly referred to as the Tax Cuts and Jobs Act of 2017 (the “Tax Act”). The Tax Act makes broad and complex changes to the U.S. tax code, including, but not limited to, reducing the U.S. federal corporate tax rate from 35 percent to 21 percent; eliminating the corporate alternative minimum tax (AMT) and changing how existing AMT credits can be realized; creating a new limitation on deductible interest expense; changing rules related to uses and limitations of net operating loss carryforwards created in tax years beginning after December 12, 2014,31, 2017; limitations on the deductibility of certain executive compensation.

In December 2017, the SEC issued Staff Accounting Bulletin No. 118 (“SAB 118”), which addresses situations where the accounting is incomplete for the income tax effects of the Act. SAB 118 directs taxpayers to consider the impact of the Act as “provisional” when the Company issued separately detachable warrants to the shareholders participating in the raise at 0.50 per share acquired. The warrantsdoes not have the following principal terms: (i)necessary information available, prepared or analyzed (including computations) to finalize the accounting for the change in tax law. Companies are provided a warrant exercise price of $2.25 per share of common stock, (ii) an exercisemeasurement period of December 12, 2015 through December 12, 2017. The underlying warrants were registered via registration statement.

Followingup to one year to obtain, prepare, and analyze information necessary to finalize the closing of the reverse merger, the Company had warrants outstanding, a majority of which were issued in conjunction with the reverse merger on December 13, 2011. As a result of the reverse merger, Pre-merged PhotoMedex shareholders were issued warrants at a ratio of 0.305836 per each outstanding share heldaccounting for provisional amounts or a total of 1,026,435 warrants. The warrants have the following principal terms: (i) a warrant exercise price of $20 per share of common stock, (ii) an exercise period of five years, and (iii) the right of the Company to notify the holders of the warrants of an earlier expiration of the warrants, at any time following such time as the Company's common stock will have had a closing trading price in excess of $30 per share for a period of 20 consecutive trading days, providedamounts that such earlier expiration date shall notcannot be earlier than that date which is 20 trading days following the delivery of such notification by the Company.
F-33


A summary of warrant transactions for the years ended December 31, 2014, 2013 and 2012 follows:
 
 
 
Number of Warrants
Weighted Average
Exercise Price
Outstanding at January 1, 20121,067,240$ 19.98
      Issued25,00020.00
      Exercised(17,756)7.50
      Expired/cancelled(11,216)47.04
Outstanding at December 31, 20121,063,268 19.91
      Issued--
      Exercised--
      Expired/cancelled(4,589)18.48
Outstanding at December 31, 20131,058,679 19.91
      Issued322,5002.25
      Exercised--
      Expired/cancelled--
Outstanding at December 31, 20141,381,179$ 15.79
At December 31, 2014, all outstanding warrants were exercisable. As the share priceestimated as of December 31, 2014 was $1.53,2017.

With regards to the aggregate intrinsic value for warrants outstanding and exercisable was immaterial.

If not previously exercised, the outstanding warrants will expire as follows:
 
 
Year Ending December 31,
 
 
Number of Warrants
Weighted Average
Exercise Price
   
201532,250$ 17.19
20161,026,42920.00
2017322,5002.25
 1,381,179$15.79
As all of the then outstanding warrants were fully vested at the date of the consummation of the reverse merger, the fair value of the warrants at that date was included as part of the calculation of the consideration transferred, as the consideration was determined basedTax Act impact on the equity interests Radiancy would have had to issuetax provision as it relates to the stockholdersCompany for the year-ending December 31, 2017, we have recognized the provisional impact of Pre-merged PhotoMedextax reform related to provide them the same equity interestsrevaluation of deferred tax assets and liabilities from 35% to 21% of $17.2 million tax expense, which is offset by a reduction in the combined company.
F-34


Note 13
Income Taxes:
valuation allowance.

Income taxes are accounted for under the asset and liability method. Deferred tax assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating loss and tax credit carryforwards. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is recognized in operations in the period that includes the enactment date.

A valuation allowance is provided when it is more likely than not that some portion or all of a deferred tax asset will not be realized. The ultimate realization of deferred tax assets is dependent upon the generation of future taxable income and the reversal of deferred tax liabilities during the period in which the related temporary difference becomes deductible. The benefit of tax positions taken or expected to be taken in the Company'sCompany’s income tax returns are recognized in the consolidated financial statements if such positions are more likely than not of being sustained.

For the years ended December 31, 2014, 2013,2016, and 2012,2015, the following table summarizes the components of income before income taxes from continuing operations and the provision for income taxes:

  
Year Ended December 31,
 
  2014  2013  2012 
Income (loss) before income tax:      
U.S. (25,398) $7,700  $3,152 
Israel  1,780   14,279   20,410 
Other Foreign  (1,813)  768   3,365 
Income (loss) before income taxes (25,431) $22,747  $26,927 
             
             
Income tax expense (benefit):            
United States -  Federal tax:            
Current (1,030) (1,253) $2,752 
Deferred  34,117   1,795   (1,572)
             
United States - State tax:            
Current  195   180   315 
Deferred:  245   850   (2,074)
             
Israel:            
Current  1,431   2,781   4,034 
Deferred  (190)  (237)  (50)
             
Other foreign:            
Current  81   54   1371 
Deferred:  1,463   200   (338)
             
Income tax expense $36,312  $4,370  $4,438 
             

  Year Ended December 31, 
  2017  2016 
Loss from continuing operations before income tax:        
U.S. $(15,684) $ 
Israel  (453)   
UK  (219)   

Loss from continuing operations before income taxes

 $(16,356) $ 
         
Income tax expense (benefit):        
United States -  Federal tax:        
Current $  $ 
Deferred      
         
United States - State tax:        
Current      
Deferred:      
         
Israel:        
Current      
Deferred       
         
UK:        
Current      
Deferred      
         
Other foreign:        
Current      
Deferred:      
         
Income tax expense (benefit) $  $ 


F-35


For the years ended December 31, 2014, 20132017 and 2012,2016, the following table reconciles the federal statutory income tax rate to the effective income tax rate:

  Year Ended December 31, 
  2017  2016 
Federal Tax rate  34%  34%
         
Federal tax expense (benefit) at 34% $(5,562) $ 
State and local income tax, net of Federal benefit  (271)   
Foreign rate differential  519    
Increase in taxes from permanent differences in stock-based compensation  333    
Increase in taxes from permanent difference in Intangible asset impairment      
US taxation of foreign earnings – Subpart F      
Return to provision and other adjustments  289    
Impact of deferred tax adjustments      
Federal Tax reform  17,192    
Change in valuation allowance  (12,500)   
         
Income tax expense (benefit) $  $            


  
Year Ended December 31,
 
  2014  2013  2012 
Federal Tax rate  34%  34%  34%
             
             
Federal tax expense (benefit) at 34% (9,349) $7,733  $9,157 
State and local income tax, net of Federal benefit  373   958   286 
Foreign rate differential  (483)  (2,404)  (3,962)
Increase in taxes from permanent differences in stock-based compensation  330   420   618 
US taxation of foreign earnings – Subpart F  11,571   357   403 
Increase (decrease) in uncertain tax positions  -   269   (2,325)
Return to provision and other adjustments  301   (1,963)  - 
Impact of tax rate change on deferred taxes  724   (942)  - 
Foreign tax credits  (7,041)  (341)  - 
Tax on foreign exchange  1,578   -   - 
Tax on undistributed earnings  3,333   -   - 
Change in valuation allowance  34,695   116   - 
Other, net  280   167   261 
             
Income tax expense $36,312  $4,370  $4,438 

As of December 31, 2014,2017, the Company had approximately $48$125 million of Federal net operating loss carryforwards in the United States. Other tax attributes in the United States and their approximate amounts include: State NOLs - $3.2 million; foreign tax credits -$7.1 million; and, AMT tax credits – $0.1 million. A 100% valuation allowance has been recorded against these tax attributes and the net deferred tax assets of the U.S. group of companies. The net deferred tax assets – liabilities of the U.S. companies is reduced to zero (0). Based on current operating conditions and the availability of projected future sources of taxable income, the Company determined that it was not more likely than not that the net deferred tax assets of the U.S. companies would be realized in the future. The StateFederal NOLs expire generally from 20172022 to 2034.

2037.

After conversion to U.S. dollars, Photo Therapeutics Limited had approximately $11$12.8 million of net operating loss carryforwards in the U.K. A 100% valuation allowance of approximately $7 million has been applied against these losses. Additionally, NOLs have been recorded in Brazil, Colombia, India, and Korea. The Brazilian NOL is approximately $1.7 million. The individual NOLs of the other companies are less than $0. 1 million. All these NOLs have a 100% valuation allowance recorded.

F-36

loss carryforwards.


The following table summarizes the components of deferred income tax assets and (liabilities):

  December 31, 
  2014  2013 
     
Loss carryforwards $39,217  $21,092 
AMT credits  112   112 
Foreign tax credits  7,066   - 
Accrued employment expenses  1,785   1,256 
Amortization and write-offs  9,480   8,883 
Capitalized R&D costs  2,663   2,933 
Deferred revenues  -   84 
Depreciation  2,022   4,360 
Doubtful accounts  4,177   3,499 
Inventory reserves  1,030   822 
Tax on undistributed earnings  (3,333)  - 
Other accruals and reserves  324   228 
Return allowances  2,787   5,660 
Translation adjustments  (44)   61 
         
Gross deferred tax asset  67,286   48,990 
         
Less: valuation allowance  (65,957)  (11,910)
         
Net deferred tax asset $1,329  $37,080 
         
Among current assets $762  $13,041 
Among other non-current assets  567   24,039 

  December 31, 
  2017  2016 
       
Loss carryforwards $29,693  $30,770 
AMT credits  112   112 
Foreign tax credits  12,308   12,308 
Accrued employment expenses  11   2,652 
Amortization and write-offs  875   1,299 
Capitalized R&D costs  1,013   1,342 
Deferred revenues     6,263 
Depreciation  635   1,224 
Doubtful accounts     225 
Inventory reserves     459 
Tax on undistributed earnings  (517)  (517)
Other accruals and reserves  1,571   602 
Return allowances     456 
         
Gross deferred tax asset  45,701   57,195 
         
Less: valuation allowance  (45,701)  (57,195)
         
Net deferred tax asset $  $ 
         
Among other non-current liabilities      

Taxes, which may apply in the event of a disposal of investments in subsidiaries, have not been included in computing the deferred taxes, as the Company anticipates it would liquidate those subsidiaries that can be closed on a tax free basis

FC Global Realty Inc. (formerly PhotoMedex, Inc.) files corporate income tax returns in the United States, both in the Federal jurisdiction and in various State jurisdictions. The Company is subject to Federal income tax examination for calendar years 20112014 through 20132017 and is also generally subject to various State income tax examinations for calendar years 20062014 through 2013.2017. Photo Therapeutics Limited files in the United Kingdom. Radiancy (Israel) Limited files in Israel. The Israeli subsidiary is subject to tax examination for calendar years 20112013 through 2013.

2017.

The Israeli subsidiary is entitled to reduced tax rates regarding income that is subject to tax pursuant to the "approved enterprise"“approved enterprise” until end of year 2012 and "preferred enterprise"“preferred enterprise” from year 2013. Other income is subject to the regular corporate income tax rate. For the year 20142015 and thereafter, all income isin Israel was taxed at the regular corporate income tax rate.

Change in Israel rates. Effective for tax periods beginning 1 January 2014, the standard corporate income tax rate was increased from 25% to 26.5% and preferred income tax rate (for preferred enterprise located in an area which is not development zone A) was increased to 16%.

Income derived from On January 4, 2016, the approved enterprise was tax-exemptplenary Knesset passed the Law for the first two years. In the succeeding five to eight years (depending on the classificationAmendment of the Company asIncome Tax Ordinance No. 216 which provides, inter alia, for a foreign-invested company) the income was taxed at a reduced rate. In the event of cash dividends from income which was tax-exempt as above, the Israeli subsidiary would have to pay 15% tax in respectreduction of the amount distributed. The Israeli subsidiary intends to reinvest the amount of such tax-exempt incomeCompanies Tax rate commencing from 2016 and not to distribute it as dividends.
The entitlement to the above benefits is contingent upon fulfillment of the conditions stipulatedthereafter by the law,rate of 1.5% such that the regulations published thereunder (and the letters of approval for the specific investments in the approved enterprise) in the preferred enterprise. Management of the Israeli subsidiary believes that as of December 31, 2014 the subsidiary was in compliance with the above-mentioned conditions. 
F-37


rate will be 25%.

Change in U.K. rates.In addition, effective for tax periods beginning on April 1, 2013,2014, the United Kingdom tax rate was reduced from 24% to 23%. A reduction from 23% to 21% was effective on April 1, 2014.. A further enacted decrease in the tax rate to 21% and 20% will taketook effect on April 1, 2015. The rate further reduced to 19% effective April 1, 2017. These changes in rate will affect the tax provision with regard to the tax attributes of Photo Therapeutics Limited, the United Kingdom subsidiary.

Unrecognized Tax Benefits.The Company is subject to income taxation in the U.S., Israel, the U.K., Brazil, Colombia, Hong Kong, India and The Republic of Korea. Colombia. Unrecognized tax benefits reflect the difference between positions taken or expected to be taken on income tax returns and the amounts recognized in the financial statements. Resolution of the related tax positions through negotiations with the relevant tax authorities or through litigation could take years to complete. It is difficult predict the timing of resolution for tax positions since such timing is not entirely within the control of the Company. It is reasonably possible that the total amount of unrecognized tax benefits could both increase and decrease in the next 12 months, with no material impact on earnings.


The Company and its subsidiaries file income tax returns in all of the countries listed above.

In 2012,

Management conducted an analysis of the facts and law surrounding the then existing income tax uncertainties, and found that such liability as may have arisen was of a much lesser magnitude and is able to be extinguished by loss carryforwards and carrybacks,

Reconciliation of the beginning and ending amount of unrecognized tax benefits is as follows:

   
Balance at January 1, 2012 $2,700 
Additions / Settlements during 2012  (2,325)
Balance December 31, 2012  375 
Additions/ Settlements due 2013  269 
Balance at December 31, 2013  644 
Additions / Settlements due 2014  - 
Balance at December 31, 2014 $644 

Balance at December 31, 2015 $1,921 
Additions / Settlements due 2016   
Balance at December 31, 2016 $1,921 
Additions / Settlements due 2017   
Balance at December 31, 2017 $1,921 

Note 14

16 

Significant Customer Concentration:

No single customer accounted for more than 10% of total company revenues of discontinued operations for the years ended December 31, 2014, 20132017 and 2012.

Note 15
Business Segment and Geographic Data:
Effective December 13, 2011, the Company reorganized its business into three operating segments to better align its organization based upon the Company's management structure, products and services offered, markets served and types of customers, as follows: The Consumer segment derives its revenues from the design, development, manufacturing and selling of long-term hair reduction and acne consumer products. The Physician Recurring segment derives its revenues from the XTRAC procedures performed by dermatologists, the sales of skincare products, the sales of surgical disposables and accessories to hospitals and surgery centers and on the repair, maintenance and replacement parts on our various products. The Professional segment generates revenues from the sale of equipment, such as lasers, medical and esthetic light and heat based products and LED products. Management reviews financial information presented on an operating segment basis for the purposes of making certain operating decisions and assessing financial performance. For a period during 2014 the Company had a fourth operating segment, Clinics segment. This represented our LCA business which is classified as discontinued operations as of December 31, 2014. See also Note 2, Discontinued Operations.
F-38

2016.


Unallocated operating expenses include costs that are not specific to a particular segment but are general to the group; included are expenses incurred for administrative and accounting staff, general liability and other insurance, professional fees and other similar corporate expenses. Interest and other financing income (expense), net is also not allocated to the operating segments. Unallocated assets include cash and cash equivalents, prepaid expenses and deposits.
The following tables reflect results of operations from our business segments for the periods indicated below:
Year ended December 31, 2014
  CONSUMER  PHYSICIAN RECURRING  PROFESSIONAL  
TOTAL
 
Revenues $120,931  $34,240  $8,370  $163,541 
Costs of revenues  20,307   12,718   5,594   38,619 
Gross profit  100,624   21,522   2,776   124,922 
Gross profit %  83.2%  62.9%  33.2%  76.4%
                 
Allocated operating expenses:                
Engineering and product development  1,105   1,177   804   3,086 
Selling and marketing expenses  89,637   16,347   1,185   107,169 
                 
Unallocated operating expenses  -   -   -   35,711 
   90,742   17,524   1,989   145,966 
Income (loss) from continuing operations  9,882   3,998   787   (21,044)
                 
Interest  and other financing expense, net  -   -   -   (4,387)
                 
Income (loss) from continuing operations before taxes $9,882  $3,998  $787  (25,431)




Year ended December 31, 2013
  CONSUMER  PHYSICIAN RECURRING  PROFESSIONAL  
TOTAL
 
Revenues $188,259  $28,548  $7,857  $224,664 
Costs of revenues  26,794   13,022   5,219   45,035 
Gross profit  161,465   15,526   2,638   179,629 
Gross profit %  85.8%  54.4%  33.6%  80.0%
                 
Allocated operating expenses:                
Engineering and product development  1,100   1,371   835   3,306 
Selling and marketing expenses  112,898   12,681   1,949   127,528 
                 
Unallocated operating expenses  -   -   -   26,750 
   113,998   14,052   2,784   157,584 
Income (loss) from operations  47,467   1,474   (146)  22,045 
                 
Interest  and other financing income, net  -   -   -   702 
                 
Net income (loss) before taxes $47,467  $1,474  (146) $22,747 
                 


F-39



Year ended December 31, 2012
  CONSUMER  PHYSICIAN RECURRING  PROFESSIONAL  
TOTAL
 
Revenues $188,425  $21,284  $10,942  $220,651 
Costs of revenues  28,965   11,512   6,165   46,642 
Gross profit  159,460   9,772   4,777   174,009 
Gross profit %  84.6%  45.9%  43.7%  78.9%
                 
Allocated operating expenses:                
Engineering and product development  876   1,201   837   2,914 
Selling and marketing expenses  102,736   10,203   3,548   116,487 
                 
Unallocated operating expenses  -   -   -   27,330 
   103,612   11,404   4,385   146,731 
Income (loss) from operations  55,848   (1,632)  392   27,278 
                 
Interest  and other financing expense, net  -   -   -   (351)
                 
Net income (loss) before taxes $55,848  (1,632) $392  $26,927 
                 

For the years ended December 31, 2014, 2013 and 2012, net revenues by geographic area (determined by ship to locations) were as follows:
  Year Ended December 31, 
  2014  2013  2012 
North America 1
 $123,161  $174,850  $163,973 
Asia Pacific 2
  9,870   19,081   28,031 
Europe (including Israel)  29,227   27,849   25,521 
South America  1,283   2,884   3,126 
  $163,541  $224,664  $220,651 
             
1 United States
 $109,203  $149,713  $135,950 
1 Canada
 $13,953  $25,137  $28,023 
Japan
 $1,750  $12,226  $21,134 
For the years ended December 31, 2014, 2013 and 2012, long-lived assets by geographic area were as follows:
  Year Ended December 31, 
  2014  2013  2012 
North America $12,385  $9,119  $5,772 
Asia Pacific  286   -   - 
Europe (including Israel)  1,127   1,370   987 
South America  4   -   - 
  $13,802  $10,489  $6,759 

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Note 16
Quarterly Financial Data (Unaudited):
  For the Quarter Ended 
2014 Mar. 31  Jun. 30*  Sep. 30*  Dec. 31 
Revenues $50,075  $38,977  $35,611  $38,878 
Gross profit  39,730   30,208   26,896   28,088 
Net loss  (345)  (7,480)  (14,943)  (98,726)
Net loss per share:                
Basic (0.02) (0.40) (0.80) (5.20)
Diluted (0.02) (0.40) (0.80) (5.20)
Shares used in computing net loss per share:                
Basic  18,719,419   18,723,484   18,724,419   19,041,451 
Diluted  18,719,419   18,723,484   18,724,419   19,041,451 
                 
2013 Mar. 31  Jun. 30  Sep. 30  Dec. 31 
Revenues $57,216  $58,065  $45,893  $63,490 
Gross profit  45,350   46,675   36,827   50,777 
Net income  7,212   7,094   886   3,185 
Net income per share:                
Basic $0.35  $0.34  $0.04  $0.16 
Diluted $0.34  $0.34  $0.04  $0.16 
Shares used in computing net income per share:                
Basic  20,678,023   20,573,048   19,982,967   19,400,341 
Diluted  21,147,583   21,033,349   20,441,262   19,602,611 
                 
2012 Mar. 31  Jun. 30  Sep. 30  Dec. 31 
Revenues $50,273  $58,906  $56,681  $54,791 
Gross profit  39,039   46,551   45,400   43,019 
Net income  4,857   4,213   7,525   5,894 
Net income per share:                
Basic $0.26  $0.20  $0.35  $0.28 
Diluted $0.26  $0.20  $0.35  $0.27 
Shares used in computing net income per share:                
Basic  18,339,977   20,547,244   21,205,675   20,947,985 
Diluted  18,876,163   21,034,814   21,752,845   21,356,819 
*The information has been retroactively adjusted to account for the LCA business which is classified as held for sale as of December 31, 2014, as a discontinued operations.
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Note 17

Valuation and Qualifying Accounts:
    Additions Charged to     
 
 
Description
 Balance at Beginning of Period  
Cost and Expenses
  
Other Accounts
  
Deductions (1)
  
Balance at End of Period
 
 
For The Year Ended December 31, 2014:
          
Allowance for Doubtful Accounts $10,734  $7,661  $-  (4,836) $13,559 
Allowance for Sales Returns $16,046  $35,771  $-  (44,166) $7,651 
 
For The Year Ended December 31, 2013:
                    
Allowance for Doubtful Accounts $6,917  $5,958  $-  (2,141) $10,734 
Allowance for Sales Returns $11,901  $47,916  $-  (43,771) $16,046 
 
For The Year Ended December 31, 2012:
                    
Allowance for Doubtful Accounts $3,196  $4,629  $-  (908) $6,917 
Allowance for Sales Returns $6,143  $43,284  $-  (37,526) $11,901 

(1)Represents write-offs of specific accounts receivable or actual returns, as applicable.
Note 18

Subsequent Events:

EffectiveEvents:

Second Closing under Securities Purchase Agreement

On January 31, 2015,24, 2018, the Company and its subsidiary LCA-Vision Inc. ("LCA")the Investor, as discussed in Note 13, completed a second closing under the Purchase Agreement, pursuant to which the Investor provided $2,225 to the Company in exchange for 2,225,000 shares of the Company’s Series B Preferred Stock. The issuance of these securities was made in reliance upon an exemption from the registration requirements of Section 5 of the Securities Act of 1933, as amended. The proceeds from this closing shall be used to perform due diligence and invest in Income Generating Properties (as defined in the Purchase Agreement) that have been approved by the Company’s Board of Directors.

Amended and Restated Separation Agreement

On February 12, 2018, the Company entered into a Stock Purchasean Amended and Restated Separation Agreement (the "Stock Purchase Agreement") with Vision Acquisition, LLC ("Vision"“Restated Agreement”), pursuant to which the Company has agreed to pay Mr. Stephen Johnson, its former Chief Financial officer, an amount of $123 in 11 installments as follows: the first 6 installments of $10 each, and the following five installments of $12.5 each. The first payment was made on February 15, 2018, and subsequent payments are to be made on or before the 15th day of each succeeding month, with the final installment to be paid on or before December 15, 2018. The Company will also provide a health (medical, dental and/or vision) insurance reimbursement payment for Mr. Johnson and his family, for a period of 11 months, in the agreed upon amount of $3 per month.

In addition, the Company has agreed to issue to Mr. Johnson 271,000 shares of the Company’s common stock, subject to appropriate adjustment for any stock splits, stock or business combinations, recapitalizations or similar events occurring after the date of the Restated Agreement. Those shares will be issued on any business day during the period commencing on the date that is six months after the date of the Restated Agreement and ending on the date that is three business days after such six-month anniversary.

Notice of Delisting or Failure to Satisfy a Continued Listing Rule or Standard; Transfer of Listing

On February 20, 2018, the Company received written notification (the “Notice”) from Nasdaq that the closing bid price of its common stock had been below the minimum $1.00 per share for the previous 30 consecutive business days, and that the Company is therefore not in compliance with the requirements for continued listing on Nasdaq under which Vision acquired LCA andNasdaq Marketplace Rule 5550(a)(2). The Notice provides the Company with an initial period of 180 calendar days, or until August 19, 2018, to regain compliance with the listing rules. The Company will regain compliance if the closing bid price of its subsidiariescommon stock is $1.00 per share or higher for a minimum period of ten consecutive business days during this compliance period, as confirmed by written notification from Nasdaq. 


If the Company does not achieve compliance by August 19, 2018, the Company expects that Nasdaq would provide notice that its securities are subject to delisting from the Company for a total purchase priceCapital Market. 

Departure and Election of $40 million in cash (the "Purchase Price"). After giving effect to working capital and indebtedness adjustments andcertain Directors

Effective March 4, 2018, Suneet Singal, the paymentCompany’s former Chief Executive Officer, has resigned from the Company’s Board of professional fees,Directors. In addition, effective March 5, 2018, Darrel Menthe has also resigned from the Company realized net proceedsCompany’s Board of approximately $36.5 million from this sale, of which $2 million was placed in escrow. The Company had originally purchased LCA in a stock-for- cash transaction which closed on May 12, 2014. Pursuant to the Termination of Joinder, dated as of January 31, 2015, LCA has been released from all of its obligations, including its guarantee and collateral obligations,Directors. Their resignations were not in connection with the Company's Credit Agreement, dated as of May 12, 2014 (as amended, restated, supplemented or otherwise modified from time to time, the "Credit Agreement"), by and betweenany known disagreement with the Company JPMorgan Chase Bank, N.A., as Administrative Agent, First Niagara Bank, N.A. and PNC Bank, National Association, each as Co-Syndication Agents, J.P. Morgan Securities LLC, as Lead Arranger and Bookrunner, and the other Lenders party thereto. The Company has used the proceeds from this transaction to pay down portions of its outstanding revolving line of credit and term loan under the Credit Agreement.

The Purchase Price was subject to working capital and indebtedness adjustments at closing, in the amount of approximately $2.1 million. The closing working capital adjustment was based upon the difference between the target net working capital and an estimated computation of LCA's net working capital as of December 31, 2014. There will also be post-closing working capital and indebtedness adjustments. Pursuant to the post-closing working capital adjustment, the purchase price paid to the Company at closing will be adjusted up or down by an amount equal to the difference between LCA's net working capital as of December 31, 2014 and LCA's net working capital as of January 31, 2015, subject to a $250,000 collar (if applicable).
F-42


The Stock Purchase Agreement contains customary representations, warranties and covenants by each of the Company, LCA and Vision, as well customary indemnification provisions among the parties.
The parties entered into several ancillary agreements as part of this transaction.
Under a Contingency Escrow Agreement among the parties, $2 million of the Purchase Price (the "Escrow Amount") has been placed into an escrow account held by Fifth Third Bank, Cincinnati, Ohio, as Escrow Agent. on any matter.

Under the termsprovisions of the Stock Purchase Agreement LCA anddated December 22, 2017 (see also Note 14), Opportunity Fund I-SS, LLC has notified the Company must obtain consentsthat it may exercise its right to appoint two replacement directors to the transactionCompany’s Board of Directors. 

Letter Agreement with OFI

Under the Purchase Agreement, the proceeds from certainthe first closing were to be used for working capital and general corporate purposes, the proceeds from the second closing were to be used to perform due diligence and invest in Income Generating Properties (as defined in the Purchase Agreement) that have been approved by the Board of LCA's vendors; a designated portionDirectors of the Escrow Amount will be released to the Company upon the receipt of each consent. If a consent is not obtained, a designated portion of the Escrow Amount may be released to Vision.

The parties have also entered into an XTRAC Exclusivity Agreement, under which LCA has granted to the Company sole and exclusive rights to provide certain excimer light source products, systems and equipment to LCA's Lasik Plus centers for the next seven years.  The terms of each placement, if any, will be determined on a center-by-center basis.
Finally, the Company, and LCAproceeds from subsequent closings were to be used to invest in Income Generating Properties (as defined in the Purchase Agreement) that have entered into a Transition Services Agreement, under which LCA will continue to provide certain accounting, human resources and call center services tobeen approved by the Board of Directors of the Company for an initial period of 60 days. During that period, the Company will arrangeor as otherwise agreed to transition those services back to the Company's own personnel and offices.
On March 10, 2015, each of the two executives, Dr. Dolev Rafaeli and Mr. Dennis McGrath, entered into Amended and Restated Employment Agreements (the "Amended Agreements") with the Company which supersede their respective Amended and Restated Employment Agreements previously entered into on August 5, 2014. 
The March 2015 Amended Agreements were required by certain provisions contained in the Second Amended and Restated Forbearance Agreement between the Company and its Lenders. Under the Amended Agreements, all cash bonusesOFI in writing prior to Dr. Rafaeli and Mr. McGrath will be deferred until the Company's repayment of the outstanding Facilities under the Credit Agreement in accordance with the provisions of the Forbearance Agreement.
Under the cash bonus provisions of the Amended Agreements (and subject to the deferral described in the preceding praagraph), Dr. Rafaeli will receive quarterly cash bonuses equal to the greater of $300,000 per calendar quarter and 1% of the Company's U.S. GAAP sales per calendar quarter in excess of targets set by the Compensation Committee, and Mr. McGrath will receive an annual cash bonus of not less than $316,000 per year. All or a portion of such bonuses may be paid in shares of Company stock to the extent mutually agreed by the Board and the executive.
The Amended Agreements also clarify the executives' rights to resign due to "Good Reason" in the event of a breach of the Amended Agreements by the Company or for any reason during the 30-day period immediately following a Change of Control ofsubsequent closings.

On March 16, 2018, the Company and OFI entered into a letter agreement, pursuant to payment of deferred bonuseswhich OFI agreed that the Company may use all proceeds for the purposes and uses described in a budget agreed to between the Company and OFI at the time the letter agreement was signed. In connection with such letter agreement, the terminationCompany agreed to provide OFI, on a quarterly basis, on or prior to 15 days after the end of their employment.each quarter, a report that describes, in reasonable detail, the actual expenses incurred, and payments made during such period compared to the expenses and payments specified in the budget for such period, certified by the Chief Financial Officer of the Company.


SIGNATURES

Pursuant to the requirements of section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized. 

Date: April 2, 2018FC GLOBAL REALTY INCORPORATED 
/s/ Vineet P. Bedi
Name: Vineet P. Bedi
Title: Chief Executive Officer

Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following persons on behalf of the registrant and in the capacities and on the dates indicated.

SignatureTitleDate
/s/ Vineet P. BediChief Executive Officer (Principal Executive Officer)April 2, 2018
Vineet P. Bedi
/s/ Matthew StolzarChief Financial Officer (Principal Financial and Accounting Officer)April 2, 2018
Matthew Stolzar
/s/ Dr. Bob FroehlichChairman of the Board of DirectorsApril 2, 2018
Dr. Bob Froehlich
/s/ Richard J. LeiderDirectorApril 2, 2018
Richard J. Leider
/s/ Dennis M. McGrathDirectorApril 2, 2018
Dennis M. McGrath
/s/ Dr. Dolev RafaeliDirectorApril 2, 2018
Dr. Dolev Rafaeli
/s/ Michael R. StewartDirectorApril 2, 2018
Michael R. Stewart

F-47

F-43