UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 10-Q

 

(Mark One)

 

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

 

For the quarterly period ended September 30, 20172019

 

or

 

[  ]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: 001-36763

 

MEDOVEX CORP.H-CYTE, INC

(Exact Namename of Registrantregistrant as Specifiedspecified in Its Charter)its charter)

 

Nevada46-3312262
(State or Other Jurisdictionother jurisdiction of(IRS Employer
of Incorporationincorporation or Organization)organization)Identification Number)No.)

201 East Kennedy Blvd, Suite 700  
3060 Royal Boulevard S Ste 150Tampa, Florida 
Alpharetta, Georgia3002233602
(Address of Principal Executive Offices)principal executive offices)(Zip Code)
(844) 633-6839

(844) 633-6839

(Registrant’s Telephone Number, Including Area Code)

Securities registered pursuant to Section 12(b) of the Act:

Title of each classTicker symbol(s)Name of each exchange on which registered
Common Stock, par value $0.001 per shareHCYTOTC Capital Markets

 

Indicate by check mark whether the registrant (1) 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 (2) has been subject to such filing requirements for the past 90 days.

[X] Yes [  ] 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 (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files.)

[X] 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 an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act.

 

Large accelerated filer [  ]Accelerated filer [  ]
Non-accelerated filer [  ]Smaller Reporting Company [X]
 (Do not check if smaller reporting company)Emerging growthGrowth Company [X]

 

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. [X]

 

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

[  ] Yes [X] No

 

As of November 14, 2017, 21,113,0232019, 99,236,413 shares of the registrant’s common stock were outstanding.

 

 

   

 

MEDOVEX CORP.H-CYTE, INC AND SUBSIDIARIES

 

TABLE OF CONTENTS

 

  Page
PART I – FINANCIAL INFORMATION2
   
Item 1.Financial Statements
Condensed Consolidated Balance Sheets as of September 30, 2017 (unaudited) and December 31, 20162
Condensed Consolidated Statements of Operations for the three and nine months ended September 30, 2017 and 2016 (unaudited)3
Condensed Consolidated Statement of Stockholders’ Equity for the nine months ended September 30, 2017 (unaudited)4
 Condensed Consolidated Balance Sheets4
Consolidated Statements of Cash Flows for the nine months ended September 30, 2017 and 2016 (unaudited)Operations5
 Consolidated Statements of Stockholders’ Equity (Deficit)6
Consolidated Statements of Cash Flows7
Notes to Condensed Consolidated Financial Statements (unaudited)68
Item 2.Management’s Discussion and Analysis of Financial Condition and Results of Operations.Operations1625
Item 3.Quantitative and Qualitative Disclosures About Market Risk.Risks2234
Item 4.Controls and Procedures.Procedures2234
   
PART II – OTHER INFORMATION 
   
Item 1.Legal Proceedings.Proceedings2235
Item 1A.Risk Factors.Factors2235
Item 2.Unregistered Sales of Equity Securities and Use of Proceeds.Proceeds2235
Item 3.Defaults Upon Senior Securities.Securities2235
Item 4.Mine Safety Disclosures.Disclosures2235
Item 5.Other Information.Information2235
Item 6.Exhibits.Exhibits2235
   
SIGNATURES2336

 

SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS

 

This Quarterly Report on Form 10-Q contains “forward-looking statements”, as defined under United States federal securities laws. These statements involve known and unknown risks, uncertainties, and other factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Forward-looking statements include, but are not limited to, statements about:

 

 our ability to market, commercialize and achieve broader market acceptance for our products;
   
 

our ability to successfully expand, and achieve full productivity from, our sales, clinical support, and marketing capabilities;
  
 our ability to successfully complete the development of, and obtain regulatory clearance or approval for, our products; and
   
 the estimates regarding the sufficiency of our cash resources, our ability to obtain additional capital or our ability to maintain or grow sources of revenue.

 

In some cases, you can identify forward-looking statements by terms such as “anticipates,” “believes,” “could,” “estimates,” “expects,” “intends,” “may,” “plans,” “potential,” “predicts,” “projects,” “should,” “will,” “would,” and similar expressions intended to identify forward-looking statements, although not all forward-looking statements contain these words. Although we believe that we have a reasonable basis for each forward-looking statement contained in this Quarterly Report, we caution you that these statements are based on a combination of facts and factors currently known by us and our projections of the future, about which we cannot be certain. You should also refer to the section of our Annual report on Form 10-K entitled “Risk Factors” for a discussion of important factors that may cause our actual results to differ materially from those expressed or implied by our forward-looking statements. As a result of these factors, we cannot assure you that the forward-looking statements in this Quarterly Report will prove to be accurate. Furthermore, if our forward-looking statements prove to be inaccurate, the inaccuracy may be material. In light of the significant uncertainties in these forward-looking statements, you should not regard these statements as a representation or warranty by us, or any other person, that we will achieve our objectives and plans in any specified time frame, or at all. We do not undertake to update any of the forward-looking statements after the date of this Quarterly Report, except to the extent required by applicable securities laws.

 

The “Risk Factors” included in the Company’s Annual Report on Form 10-K reflect the “Risk Factors” of H-CYTE (formerly MedoveX) business and do not include information relative to Regenerative Medicine Solutions, LLC, RMS Shareholder, LLC (“Shareholder”), Lung Institute LLC (“LI”), RMS Lung Institute Management LLC (“RMS LI Management”) and Cognitive Health Institute Tampa, LLC (“CHIT”), (collectively “RMS”).

PART I – FINANCIAL INFORMATION

 

Item 1. Financial Statements

H-CYTE, INC AND SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

 

  September 30, 2019 (Unaudited)  December 31, 2018 
       
Assets        
         
Current Assets        
Cash $367,877  $69,628 
Accounts receivable  37,180   15,242��
Other receivables  33,868   5,144 
Inventory  126,250    
Prepaid expenses  198,927   59,678 
Total Current Assets  764,102   149,692 
         
Right-of-use asset  859,134    
Property and equipment, net  235,225   266,916 
Intangibles, net  3,128,000    
Goodwill  12,564,401    
Other assets  29,239   38,288 
Total Assets $17,580,101  $454,896 
         
Liabilities and Stockholders’ Equity (Deficit)        
         
Current Liabilities        
Interest payable $78,328  $158,371 
Accounts payable  1,952,500   851,604 
Accrued liabilities  543,137   183,183 
Other current liabilities  532,396   462,856 
Short-term note, related party  1,250,000   180,000 
Short-term financing payable  114,123   30,852 
Short-term convertible notes payable  774,615    
Notes payable, current portion  71,653    
Dividend payable  105,389    
Deferred revenue  1,364,658   326,064 
Lease liability, current portion  481,295    
Total Current Liabilities  7,268,094   2,192,930 
         
Long-Term Liabilities        
Lease liability, net of current portion  396,424    
Notes payable, net of current portion  22,920    
Convertible debt to related parties     4,306,300 
Derivative liability - warrants  332,150    
Deferred rent     22,206 
Total Long-Term Liabilities  751,494   4,328,506 
         
Total Liabilities  8,019,588   6,521,436 
         
Commitments and Contingencies (Note 10)        
         
Stockholders’ Equity (Deficit)        
Series A Convertible Preferred Stock - $.001 par value: 500,000 shares authorized, no shares issued and outstanding at September 30, 2019 and December 31, 2018      
Series B Convertible Preferred Stock - $.001 par value: 10,000 shares authorized, 7,000 and 0 shares issued and outstanding at September 30, 2019 and December 31, 2018, respectively  7    
Series C Convertible Preferred Stock - $.001 par value: 45,000 shares authorized, no shares issued and outstanding at September 30, 2019 and December 31, 2018      
Common stock - $.001 par value: 199,000,000 and 49,500,000 shares authorized. 99,236,360 and 33,661,388 shares issued and outstanding at September 30, 2019 and December 31, 2018, respectively  99,237   33,661 
Additional paid-in capital  25,818,913   3,566,339 
Accumulated deficit  (15,987,512)  (9,296,408)
Non-controlling interest  (370,132)  (370,132)
Total Stockholders’ Equity (Deficit)  9,560,513   (6,066,540)
         
Total Liabilities and Stockholders’ Equity (Deficit) $17,580,101  $454,896 

See accompanying notes to the unaudited consolidated financial statements

MEDOVEX CORP.H-CYTE, INC AND SUBSIDIARYSUBSIDIARIES

CONDENSED CONSOLIDATED BALANCE SHEETSSTATEMENTS OF OPERATIONS

(Unaudited)

 

  September 30, 2017  December 31, 2016 
 (unaudited)    
Assets      
Current Assets        
Cash $1,930,780  $892,814 
Accounts receivable  94,779    
Other receivables  23,369    
Inventory  164,867    
Prepaid expenses  140,406   364,822 
Short-term receivable  150,000    
Total Current Assets  2,504,201   1,257,636 
Long Term Receivable     150,000 
Property and Equipment, net of accumulated depreciation  92,398   97,590 
Deposits  2,751   2,751 
Total Assets $2,599,350  $1,507,977 
Liabilities and Stockholders’ Equity (Deficit)        
Current Liabilities        
Interest payable $69,222  $69,222 
Accounts payable  268,831   225,725 
Accounts payable to related parties  671    
Accrued liabilities  135,000   459,800 
Notes payable, current portion  62,147   126,086 
Short-term note payable, net of debt discount     970,240 
Total Current Liabilities  535,871   1,851,073 
Long-Term Liabilities        
Notes payable, net of current portion  55,336   103,742 
Deferred rent  983   1,179 
Total Long-Term Liabilities  56,319   104,921 
Total Liabilities  592,190   1,955,994 
Stockholders’ Equity (Deficit)        
Preferred stock - $.001 par value: 500,000 shares authorized, 12,740 shares issued and outstanding at September 30, 2017 (unaudited), no shares issued and outstanding at December 31, 2016  13    
Common stock - $.001 par value: 49,500,000 shares authorized, 20,922,634 and 14,855,181 shares issued and outstanding at September 30, 2017  (unaudited) and December 31, 2016, respectively  20,923   14,855 
Additional paid-in capital  33,188,741   25,898,054 
Accumulated deficit  (31,202,517)  (26,360,926)
Total Stockholders’ Equity (Deficit)  2,007,160   (448,017)
Total Liabilities and Stockholders’ Equity (Deficit) $2,599,350  $1,507,977 
  

Three Months Ended

September 30,

  

Nine Months Ended

September 30,

 
  2019  2018  2019  2018 
Revenues $2,742,442  $1,536,990  $6,498,404  $6,880,794 
Cost of Sales  (550,139)  (503,755)  (1,539,104)  (1,979,128)
Gross Profit  2,192,303   1,033,235   4,959,300   4,901,666 
                 
Operating Expenses                
Salaries and related costs  1,913,845   894,773   7,078,531   3,072,807 
Other general and administrative  2,025,980   809,119   5,309,791   2,482,789 
Advertising  1,467,691   278,942   4,188,087   1,435,784 
Depreciation & amortization  211,885   35,371   631,722   84,259 
Total Operating Expenses  5,619,401   2,018,205   17,208,131   7,075,639 
                 
Operating Loss  (3,427,098)  (984,970)  (12,248,831)  (2,173,973)
                 
Other Income (Expense)                
Other income  --   --   2,153   -- 
Foreign currency transaction gain  --   --   6,837   -- 
Change in fair value of derivative liability - warrants  883,527   --   883,527   -- 
Interest expense  (80,092)  (50,281)  (259,436)  (121,200)
Total Other Income (Expenses)  803,435   (50,281)  633,081   (121,200)
                 
Net Loss $(2,623,663) $(1,035,251) $(11,615,750) $(2,295,173)
                 
Dividend on outstanding Series B Preferred Stock  21,000   --   66,639   -- 
Deemed dividend on adjustment to exercise price on convertible debt and certain warrants  --   --   404,384   -- 
Deemed dividend on beneficial conversion features  --   --   32,592   -- 
Net loss attributable to common stockholders $  (2,644,663) $(1,035,251) $(12,119,365) $(2,295,173)
                 
Loss per share – Basic and Diluted $(0.03) $(0.03) $(0.13) $(0.07)
Weighted average outstanding shares used to compute basic and diluted net loss per share  98,991,805   33,661,388   96,150,811   33,661,388 

 

See accompanying notes to condensedthe unaudited consolidated financial statements

 

5 -2-
 

 

MEDOVEX CORP.H-CYTE, INC AND SUBSIDIARYSUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(UNAUDITED)

  Three Months Ended
September 30,
  

Nine Months Ended

September 30,

 
  2017  2016  2017  2016 
Revenues $117,277  $  $117,277  $ 
Cost of Goods Sold  (96,683)     (96,683)   
Gross Profit  20,594      20,594    
                 
Operating Expenses                
General and administrative 1,092,084  1,230,833  3,540,500  3,384,322 
Sales and marketing  216,950   107,001   444,708   166,240 
Research and development  70,151   395,752   461,924   772,238 
Depreciation  7,109   2,033   20,000   6,042 
Impairment of goodwill           6,455,645 
Total Operating Expenses  1,386,294   1,735,619   4,467,132   10,784,487 
                 
Operating Loss  (1,365,700)  (1,735,619)  (4,446,538)  (10,784,487)
                 
Other Expenses                
Interest expense  1,654   15,887   393,890   359,981 
Total Other Expenses  1,654   15,887   393,890   359,981 
                 
Total Loss from Continuing Operations  (1,367,354)  (1,751,506)  (4,840,428)  (11,144,468)
                 
Discontinued Operations                
Loss from discontinued operations     57,023   1,163   456,083 
Impairment loss           1,584,048 
Total Loss from Discontinued Operations     (57,023)  (1,163)  (2,040,131)
                 
Net Loss $(1,367,354) $(1,808,529) $(4,841,591) $(13,184,599)
Loss per share – Basic and Diluted:                
Continuing Operations $(0.07) $(0.13) $(0.26) $(0.87)
Discontinued Operations           (0.16)
Net Loss per share $(0.07) $(0.13) $(0.26) $(1.03)
                 
Weighted average outstanding shares used to compute basic and diluted net loss per share  20,504,932   13,847,346   18,332,398   12,843,008 

See notes to condensed consolidated financial statements

 -3-

MEDOVEX CORP. AND SUBSIDIARY

CONDENSEDCONSOLIDATED STATEMENT OF STOCKHOLDERS’ EQUITY (DEFICIT)

For the three and nine months ended September 30, 20172019

(Unaudited)

 

  Common Stock  Preferred Stock  Additional  Accumulated  Total  Stockholders’ 
  Shares  Amount  Shares  Amount  Paid-in Capital  Deficit  Equity 
Balance – December 31, 2016  14,855,181  $14,855     $  $

25,898,054

  $(26,360,926) $(448,017)
Issuance of common stock in exchange for BOD fees in January 2017  173,912   174         239,826      240,000 
Issuance of common stock pursuant to a private placement complete in February 2017  1,631,730   1,632         794,602      796,234 
Issuance of preferred stock pursuant to a private placement completed in February 2017        12,740   13   1,019,798      1,019,811 
Issuance of warrants pursuant to a private placement completed in February 2017              802,014      802,014 
Issuance of common stock pursuant to the conversion of a short term note in February 2017  165,865   166         126,554      126,720 
Issuance of preferred stock pursuant to the conversion of a short term note in February 2017        

9,399

   

9

   718,070      718,079 
Issuance of warrants pursuant to the conversion of a short term note in February 2017              305,201      305,201 
Issuance of common stock pursuant to warrant cancellations in February 2017  200,000   200         207,800      208,000 
Issuance of common stock pursuant to preferred stock conversion in March 2017  414,663   415   (4,147)  (4)  (411)      
Issuance of common stock pursuant to preferred stock conversion in April 2017  525,240   525   (5,252)  (5)  (520)      
Issuance of common stock pursuant to a private placement completed in July 2017  2,956,043   2,956         2,019,670      2,022,626 
Issuance of warrants pursuant to a private placement completed in July 2017              446,561      446,561 
Stock based compensation              611,522      611,522 
Net loss                 

(4,841,591

)  

(4,841,591

)
Balance – September 30, 2017  20,922,634  $20,923   12,740  $13  $

33,188,741

  $(31,202,517) $

 2,007,160

 
For the Three Months Ended Preferred Stock  Common Stock  Additional Paid-in  Accumulated  Non-controlling  Total Stockholders’
(Deficit)
 
September 30, 2019 Shares  Amount  Shares  Amount  Capital  Deficit  Interest  Equity 
Balances – June 30, 2019  7,000  $7   98,886,360  $98,887  $25,705,975  $(13,480,691) $(370,132) $11,954,046 
Issuance of common stock in connection with private placement offering        200,000   200   77,164         77,364 
Issuance of warrants in connection with private placement offering              22,636         22,636 
Issuance of common stock in exchange for consulting services        150,000   150   43,349         43,499 
Derivative liability adjustment (Note12)              (116,842)  116,842      

 

— 

Issuance of warrants pursuant to extension of maturity date on convertible debt              106,158         106,158 
Stock based compensation              1,473         1,473 
Dividends payable              (21,000)        (21,000)
Net loss                 (2,623,663)     (2,623,663)
Balances - September 30, 2019  7,000  $7     99,236,360  $  99,237  $  25,818,913  $(15,987,512) $(370,132) $9,560,513 

For the Nine Months Ended Preferred Stock  Common Stock  Additional Paid-in  Accumulated  Non-controlling  Total Stockholders’
(Deficit)
 
September 30, 2019 Shares  Amount  Shares  Amount  Capital  Deficit  Interest  Equity 
Balances - December 31, 2018    $   33,661,388  $33,661  $3,566,339  $(9,296,408) $(370,132) $(6,066,540)
Purchase accounting entries due to the purchase transaction  9,250   9   24,717,217   24,717   12,657,182         12,681,908 
Adjustment for assets and liabilities not included in purchase transaction                 5,244,780      5,244,780 
Issuance of common stock in connection with private placement offering        17,700,000   17,700   4,402,087         4,419,787 
Issuance of warrants in connection with private placement offering              2,663,797         2,663,797 
Issuance of common stock pursuant to conversion of short-term debt        500,000   500   125,437         125,937 
Issuance of warrants pursuant for repayment of short-term debt              74,063         74,063 
Issuance of additional exchange shares (Note 3)        17,263,889   17,264   (17,264)         
Issuance of common stock pursuant to conversion of convertible short-term debt        250,000   250   99,750         100,000 
Conversion of Preferred Series B Stock and accrued dividends  (2,250)  (2)  604,167   605   (603)         
Issuance of common stock to pay accrued interest on convertible short-term debt        1,667   2   665         667 
Issuance of common stock in exchange for consulting fees incurred        280,085   280   95,253         95,533 

Adjustment of exercise price on convertible debt 

              287,542   (287,542)      
Issuance of common stock to pay accrued dividends on Preferred Series B stock        32,313   32   12,894         12,926 
Beneficial conversion on Preferred Series B Stock              32,592   (32,592)      
Issuance of common stock per restricted stock award to executive (Note 9)        4,225,634   4,226   1,686,028         1,690,254 
Issuance of warrants pursuant to extension of maturity date on convertible debt              106,158         106,158 
Stock based compensation              93,632         93,632 
Dividends payable              (66,639)        (66,639)
Net loss                 (11,615,750)     (11,615,750)
Balances - September 30, 2019  7,000  $7     99,236,360  $99,237  $  25,818,913  $(15,987,512) $(370,132) $9,560,513 

 

See accompanying notes to condensedthe unaudited consolidated financial statements

 -4-

MEDOVEX CORP.H-CYTE, INC AND SUBSIDIARYSUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(UNAUDITED)(Unaudited)

 

  Nine Months Ended September 30, 
  2017  2016 
Cash Flows from Operating Activities        
Net loss $(4,841,591) $(13,184,599)
Adjustments to reconcile net loss to net cash used in operating activities:        
Depreciation  20,000   6,171 
Amortization of intangible assets     189,522 
Amortization of debt discount  31,772   261,973 
Debt conversion expense  355,985   68,694 
Impairment loss     1,584,048 
Goodwill impairment loss     6,455,645 
Stock based compensation  611,522   562,209 
Straight-line rent adjustment  (196)  688 
Non-cash consulting services     249,300 
Non-cash directors fees     15,000 
Adjustment of fair value of warrant modification     25,720 
Changes in operating assets and liabilities, net of effects of acquisition:        
Accounts receivable  (94,779)  33,045 
Other receivables  (23,369)   
Prepaid expenses  224,416   (368,165)
Inventory  (164,867)   
Accounts payable  43,106   (80,152)
Accounts payable to related parties  671    
Interest payable     (2,061)
Accrued liabilities  (84,800)  173,427 
Net Cash Used in Operating Activities  (3,922,130)  (4,009,535)
         
Cash Flows from Investing Activities        
Expenditures for property and equipment  (14,808)  (6,221)
Net Cash Used in Investing Activities  (14,808)  (6,221)
Cash Flows from Financing Activities        
Principal payments under note payable obligations  (112,342)  (111,530)
Proceeds from issuance of common and preferred stock, net of offering costs  3,838,671   1,934,622 
Proceeds from issuance of warrants, net of offering costs  1,248,575   541,648 
Proceeds from issuance of short term loan     995,000 
Net Cash Provided by Financing Activities  4,974,904   3,359,740 
Net Increase/(Decrease) in Cash  1,037,966   (656,016) 
Cash - Beginning of period  892,814   1,570,167 
Cash - End of period $1,930,780  $914,151 
Supplementary Cash Flow Information        
Cash paid for interest $

6,130

  $6,168 
Non-cash investing and financing activities        
Financing agreement for insurance policy $66,895  $ 
Conversion of note and accrued interest to common stock  718,079   1,072,513 
Conversion of short-term loan to common stock  126,720    
Issuance of warrants for conversion of notes  305,201    
Issuance of common stock for consulting services     249,300 
Common stock issued for board fees  240,000    
Issuance of common stock for preferred stock conversion  931    
Issuance of common stock warrants for placement agent fees  304,183    
Repayment of due from stockholder through foregone director fees     15,000 
Issuance of common stock for consideration of cancellation of warrants  

208,000

    

  Nine Months Ended 
  September 30, 2019  September 30, 2018 
Cash Flows from Operating Activities        
Net loss $(11,615,750) $(2,295,173)
Adjustments to reconcile net loss to net cash used in operating activities:        
Depreciation and amortization  631,722   84,259 
Amortization of debt discount  151,881   -- 
Interest and penalties on extension of short-term convertible notes  124,615   -- 
Stock-based compensation  1,783,886   -- 
Loss on write-off of inventory  5,205   -- 
Common stock issued for consulting services  95,533   -- 
Income from change in fair value adjustment of derivative liability - warrants  (883,527)  -- 
Issuance of warrants to extend short-term debt  106,158   -- 
Bad debt expense  60,112   -- 
Changes in operating assets and liabilities, net of purchase transaction:        
Accounts receivable  63,707   (6,903)
Other receivables  (28,724)  -- 
Accounts receivable from related parties  --   (8,824)
Prepaid expenses and other assets  (140,304)  89,078 
Interest payable  (25,381)  98,286 
Accounts payable  486,196   207,265 
Accrued liabilities  (102,099)  (96,667)
Other current liabilities  354,340   (57,801)
Dividend payable  (12,928)  -- 
Deferred revenue  1,038,594   (391,938)
         
Net Cash Used in Operating Activities  (7,906,764)  (2,378,418)
         
Cash Flows from Investing Activities        
Purchases of property and equipment  (17,238)  (207,895)
Purchase of business, net of cash acquired  (302,710)  -- 
assets not included in purchase transaction  (69,629)  -- 
Net Cash Used in Investing Activities  (389,577)  (207,895)
         
Cash Flows from Financing Activities        
Payments on short-term related party notes  (180,000)  (4,944)
Proceeds from short-term related party notes  1,250,000   -- 
Payment of dividends  (6,136)  -- 
Proceeds from debt obligations  277,519   50,020 
Payment on debt obligations  (130,377)  -- 
Proceeds from common stock  4,419,787   -- 
Proceeds from warrants  2,663,797   -- 
Proceeds from shareholder contributions  300,000   -- 
Proceeds from convertible debt to a related party  --   2,367,724 
Net Cash Provided by Financing Activities  8,594,590   2,412,800 
         
Net Increase (Decrease) in Cash  298,249   (173,513)
         
Cash - Beginning of period  69,628   251,330 
         
Cash - End of period $367,877  $77,817 
         
Supplementary Cash Flow Information        
Cash paid for interest $132,937  $20,900 
         
Non-cash investing and financing activities        
Common stock issued to pay accrued dividends $12,928  $-- 
Deemed dividends $436,976  $-- 
Conversion of debt obligations to common stock $225,937  $-- 
Conversion of debt obligations to warrants $74,063  $-- 
Issuance of warrants to extend short-term debt $106,158  $-- 
Conversion of short-term related party notes payable to common stock $114,000  $-- 
Conversion of note and accrued interest to common stock and warrants $607  $-- 
Interest and penalties on extension of short-term convertible notes $253,607  $-- 
Dividends accrued $66,639  $-- 
Repurchase of non-controlling interest $--  $33,805 

 

See accompanying notes to condensedthe unaudited consolidated financial statements

 -5-

 

MEDOVEX CORP.H-CYTE, INC

NOTES TO THE UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

 

Note 1 - Description of the Company

MedoveX Corp. (the “Company” or “MedoveX”) was incorporated in Nevada onOn July 30, 2013 as SpineZ11, 2019, Medovex Corp. (“SpineZ”MedoveX”) and changed its namenamed to MedoveX Corp. on March 20, 2014. MedoveX isH-CYTE, Inc. (“H-CYTE” or the parent company“Company”) by filing a Certificate of Debride Inc. (“Debride”Amendment (the “Amendment”), which was incorporated under to the lawsCompany’s Amended and Restated Certificate of Incorporation (the “Certificate of Incorporation”) with the Secretary of the State of Nevada. The name change and the Company’s new symbol, HCYT, became effective with FINRA on July 15, 2019.

On October 18, 2018, H-CYTE (formerly named MedoveX) entered into an Asset Purchase Agreement (“APA”) with Regenerative Medicine Solutions, LLC, RMS Shareholder, LLC (“Shareholder”), Lung Institute LLC (“LI”), RMS Lung Institute Management LLC (“RMS LI Management”) and Cognitive Health Institute Tampa, LLC (“CHIT”), (collectively “RMS”). On January 8, 2019, the APA was amended, and the Company acquired certain assets and assumed certain liabilities of RMS as reported in the 8-K/A filed in March of 2019. Based on the terms of the APA and its amendment (collectively the “APA”), the former RMS members had voting control of the combined company as of the closing of the RMS acquisition. For accounting purposes, the acquisition transaction has been treated as a reverse acquisition whereby the Company is deemed to have been acquired by RMS and the historical financial statements prior to the acquisition date of January 8, 2019 now reflect the historical financial statements of RMS.

Prior to the merger of H-CYTE and RMS on January 8, 2019 (the “Merger”), the consolidated results for H-CYTE include the financial activities of Regenerative Medicine Solutions, LLC, LI, RMS Nashville, LLC (“Nashville”), RMS Pittsburgh, LLC (“Pittsburgh”), RMS Scottsdale, LLC (“Scottsdale”), RMS Dallas, LLC (“Dallas”), State, LLC (“State”), Cognitive Health Institute of Tampa (“CHIT”), RMS LI Management, and Shareholder, H-CYTE included Lung Institute Dallas, PLLC (“LI Dallas”), Lung Institute Nashville, PLLC (“LI Nashville”), Lung Institute Pittsburgh, PLLC (“LI Pittsburgh”), and Lung Institute Scottsdale, LLC (“LI Scottsdale”), as Variable Interest Entities (“VIEs”).

As of the merger, the consolidated results for H-CYTE include the following wholly-owned subsidiaries: H-CYTE Management, LLC (formerly Blue Zone Health Management, LLC), Cognitive Health Institute, LLC, and Lung Institute Tampa, LLC (formerly Blue Zone Lung Tampa, LLC). Additionally, H-CYTE has consolidated LI Dallas, LI Nashville, LI Pittsburgh, and LI Scottsdale, as VIEs.

The Company’s RMS division is a healthcare medical biosciences company that develops and implements advanced innovative treatment options in regenerative medicine to treat an array of debilitating medical conditions. In addition, the company is the operator and manager of the various Lung Health Institute clinics. Committed to an individualized patient-centric approach, RMS consistently provides oversight and management of the highest quality care while producing positive outcomes. RMS offices are located in Tampa, Florida. The Lung Health Institute located in Tampa, Florida is a wholly owned subsidiary of RMS. RMS also provides oversight and management to the Lung Health Institutes located in Nashville, TN, Scottsdale AZ, Pittsburgh, PA, and Dallas, TX.

On June 21, 2019, H-CYTE entered into an agreement with Rion, LLC (“Rion”) to develop a disruptive cytotherapy technology for chronic obstructive pulmonary disease (“COPD”), the fourth leading cause of death in the U.S. This agreement provides for a 10-year exclusive and extendable supply agreement with Rion to enable H-CYTE to develop proprietary biologics. This will be managed through a new Rion division of H-CYTE.

Rion has established a novel technology to harness the healing power of the body. Rion’s novel exosome technology, based on October 1, 2012. science developed at Mayo Clinic, provides an off-the-shelf platform to enhance healing in soft tissue, musculoskeletal, cardiovascular and neurological organ systems.

With this agreement, Rion will serve as the product supplier and co-develop a proprietary cellular platform with H-CYTE for the treatment of COPD, and H-CYTE will control the commercial development and facilitate clinical trial investigation. After conducting joint research and development of these biologics, H-CYTE intends to pursue submission of an investigational new drug (IND) application for review by the U.S. Food and Drug Administration (“FDA”) for treatment of COPD.

The Company is also in the business of designing and marketing proprietary medical devices for commercial use in the United States and Europe. The Company received CE marking in June 2017 for the DenerveX System, and it is now commercially available throughout the European Union and several other countries that accept CE marking. The Company’s first sale of the DenerveX System occurred in July 2017. The Company plansis presently reevaluating its approaches to revenue generation including the continuing use of its distribution channels, source of manufacturing, and evaluating joint venture opportunities. In July 2019, the Company signed a new engineering feasibility proposal that would confirm a new sterilization process which would be a slightly less expensive option and expand the shelf life of DenerveX from six months to a minimum of one year and potentially up to three years. The longer shelf life will help the distributors reach more end-users as many hospital systems and medical practitioners will not purchase medical products with less than a one-year shelf life. The Company still considers the United States to be a target market and it remains the Company’s goal to seek approval for the DenerveX System from the Food & Drug Administration (“FDA”)FDA approval. The Company anticipates that it will do so once it is back in the United States.production and generating revenue through sales in Europe and other approved countries.

8

 

Note 2 – Basis of presentation and Summary of Significant Accounting Policies

Based on the terms of the APA, the former RMS members had voting control of the combined company as of the closing of the Merger. RMS is deemed to be the acquiring company for accounting purposes and the transaction is accounted for as a reverse acquisition under the acquisition method of accounting for business combinations in accordance with accounting principles generally accepted in the United States (“U.S. GAAP”). The assets acquired and the liabilities assumed of RMS included as part of the purchase transaction are recorded at historical cost. Accordingly, the assets and liabilities of H-CYTE are recorded as of the merger closing date at their estimated fair values (see Note 3).

The unaudited consolidated balance sheets, consolidated statements of operations, consolidated statements of stockholders’ equity (deficit), and the consolidated statements of cash flows do not reflect the historical financial information related to H-CYTE prior to the Merger as they only reflect the historical financial information related to RMS. For the unaudited consolidated statements of stockholders’ equity (deficit), the common stock, preferred stock, and additional paid in capital reflect the accounting for the stock received by the RMS members as of the Merger as if it was received at the beginning of the periods presented. The unaudited consolidated statements of stockholders’ equity (deficit) reflect the activity from June 30, 2019 to September 30, 2019 and December 31, 2018 to September 30, 2019. For the comparable period from December 31, 2017 to September 30, 2018, the only activity in the unaudited consolidated statement of stockholders’ equity (deficit) were the losses totaling approximately $1,035,251 and $2,295,173 for the three and nine months ended September 30, 2018, respectively.

 

The accompanying unaudited condensed consolidated financial statements have been prepared in accordance with United States (“U.S.”) generally accepted accounting principles (“GAAP”) GAAP and with the rules and regulations of the Securities and Exchange Commission (“SEC”) that permit reduced disclosure for interim periods. The unaudited interim condensed consolidated financial statements have been prepared on the same basis as the annual consolidated financial statements and, in the opinion of management, reflect all adjustments which included only normal recurring adjustments, necessary to present fairly the Company’s financial position as of September 30, 20172019 and December 31, 2016,2018 and the results of operations for the three and nine months ended September 30, 20172019 and 2016,2018 and statements of cash flows for the nine months ended September 30, 20172019 and 2016. 2018.

These unaudited condensed consolidated financial statements should be read in conjunction with the consolidated financial statements, and notes thereto for the fiscal year ended December 31, 2016,2018, included in the Company’s Annual Report on Form 10-K. The December 31, 2018 financial information included in the Company’s Annual Report on Form 10-K reflect the historical financial information of the H-CYTE business and do not include the RMS financial information. With the reverse merger, historical financial information for periods prior to the merger on January 8, 2019, presented in the comparative financial information included in the 2019 Form 10-Q, will only reflect the historical financial information related to RMS prior to the merger (see Note 3).

The results for the three and nine months ended September 30, 20172019 are not necessarily indicative of the results to be expected for the year ending December 31, 20172019 or for any other interim period or for any future year.

principlesPrinciples of consolidationConsolidation

 

TheseU.S. GAAP requires that a related entity be consolidated with a company when certain conditions exist. An entity is considered to be a VIE when it has equity investors who lack the characteristics of having a controlling financial interest, or its capital is insufficient to permit it to finance its activities without additional subordinated financial support. Consolidation of a VIE by the Parent would be required if it is determined that the Parent will absorb a majority of the VIE’s expected losses or residual returns if they occur, retain the power to direct or control the VIE’s activities, or both.

The accompanying unaudited condensed consolidated financial statements that presentinclude the Company’s resultsaccounts of operationsthe parent, its wholly-owned subsidiaries, and its VIEs.

Accounts Receivable

Accounts receivable represent amounts due from customers for which revenue has been recognized. Generally, the Company does not require collateral or any other security to support its receivables. Trade accounts receivable are stated net of an estimate made for doubtful accounts, if any. Management evaluates the adequacy of the allowance for doubtful accounts regularly to determine if any account balances will potentially be uncollectible. Customer account balances are considered past due or delinquent based on the contractual agreement with each customer. Accounts are written off when, in management’s judgment, they are considered uncollectible. At September 30, 2019 and December 31, 2018, management believes no allowance is necessary. For the three and nine monthsmonth periods ended September 30, 20172019, the Company recorded bad debt expense of approximately $0 and 2016,$60,000, respectively.

Goodwill And Intangibles

Goodwill is recorded at fair value and cash flowsnot amortized but is reviewed for impairment at least annually or more frequently if impairment indicators arise. Goodwill is evaluated for impairment by first performing a qualitative assessment to determine whether a quantitative goodwill test is necessary. If it is determined, based on qualitative factors, that the fair value is “more likely than not” less than the carrying amount or if significant changes related to the business have occurred that could materially impact fair value, a quantitative goodwill impairment test would be required. The Company can elect to forego the qualitative assessment and perform the quantitative test.

If the carrying amount exceeds its fair value, “Step 1” is performed to determine if goodwill is impaired and to measure the amount of impairment loss to recognize, if any. This step compares the implied fair value of goodwill with the carrying amount of goodwill. If the carrying amount of goodwill exceeds the implied fair value, an impairment loss is recognized in an amount equal to that excess.

The implied fair value of goodwill is determined by assigning the fair value to all the assets and liabilities of that unit (including any unrecognized intangible assets) as if the reporting unit had been acquired in a business combination. The Company has elected to perform the annual impairment assessment for goodwill in the fourth quarter.

Intangibles acquired in a business combination are recorded at fair value using generally accepted valuation methods appropriate for the nine months endedtype of intangible asset. Intangible assets with definite lives are amortized over the estimated useful lives and are reviewed for impairment whenever events or changes in circumstances indicate that the carrying value may be greater than fair value. The Company’s intangible assets are patents and related proprietary technology for the DenerveX System.

Leases

In February 2016, the Financial Accounting Standard Board (“FASB”) established Topic 842, Leases, by issuing Accounting Standards Update (ASU) No. 2016-02 (as amended), which requires lessees to recognize leases on the balance sheet and disclose key information about leasing arrangements. The new standard establishes a right-of-use (“ROU”) model that requires a lessee to recognize a ROU asset and lease liability on the balance sheet for all leases with a term longer than twelve months. Leases will be classified as finance or operating, with classification affecting the pattern and classification of expense recognition in the statement of operations.

The Company has not entered into significant lease agreements in which it is the lessor. For the lease agreements in which the Company is lessee, under Topic 842, lessees are required to recognize a lease liability and right-of-use asset for all leases (with the exception of short-term leases) at the lease commencement date. Effective January 1, 2019, the Company adopted this guidance, applied the modified retrospective transition method and elected the transition option to use the effective date as the date of initial application. The Company recognized the cumulative effect of the transition adjustment on the consolidated balance sheet as of the effective date and did not provide any new lease disclosures for periods before the effective date. With respect to the practical expedients, the Company elected the package of transitional-related practical expedients and the practical expedient not to separate lease and non-lease components.

Other Receivables

Other receivables totaling approximately $34,000 at September 30, 20172019 include receivables from the non-acquired Lung Institute, LLC due to Lung Institute Tampa, LLC for approximately $19,000, and 2016, include Debride and the accountsapproximately $9,000 reimbursement receivable for reimbursement of expenses from a joint study. The $19,000 receivable was a result of the Lung Institute, LLC being a transitory entity for Lung Institute Tampa, LLC while the merchant services accounts are being transferred.

Revenue Recognition

The Company recognizes revenue in accordance with U.S. GAAP as welloutlined in the FASB ASC 606,Revenue From Contracts with Customers, which requires that five steps be completed to determine when revenue can be recognized: (i) identify the contract with the customer; (ii) identity the performance obligations in the contract; (iii) determine the transaction price; (iv) allocate the transaction price; and (v) recognize revenue when or as the entity satisfies a performance obligation. The Company records revenue under ASC 606 when control is transferred to the customer, which is consistent with past practice. The adoption of this standard did not have a material impact on the consolidated financial statements.

Biomedical Services

H-CYTE wholly owns the Tampa, Florida Lung Health Institute (LHI) location and manages the other Lung Health Institute locations. The Lung Health Institute uses a standard pricing model for the types of cellular therapy treatments that is offered to its formerly wholly-owned subsidiary, Streamline Inc. (“Streamline”). All intercompanypatients. The transaction price accounts for medical, surgical, facility, and transactions have been eliminatedoffice services rendered by LHI for consented procedures and is recorded as revenue. The company recognizes revenue when the terms of a contract with a patient are satisfied.

The Lung Health Institute locations offer two types of cellular therapy treatments to their patients. The first type of treatment includes medical services rendered typically over a two-day period in consolidation.which the patient receives cellular therapy. For this treatment type, revenue is recognized in full at time of service. LHI also offers a four-day treatment in which medical services are rendered typically over a two-day period and then again, approximately three months later, medical services are rendered for an additional two days of treatment. Payment is collected in full for both service periods at the time the first treatment is rendered. Revenue is recognized when services are performed based on the related professional, facility, and diagnostic services for each session of treatment. The Company has deferred recognition of revenue amounting to approximately $1,365,000 and $326,000 at September 30, 2019 and December 31, 2018, respectively.

 

Use of Estimates

 

In preparing the unaudited consolidated financial statements, U.S. GAAP requires disclosure regarding estimates and assumptions used by management that affect the amounts reported in financial statements and accompanying notes. The Company’s significant estimates include deferred revenue, the deferred income tax asset and the related valuation allowance, andbusiness acquisition accounting, the fair value of its share basedwarrant issuances and share-based payment arrangements.

 

For those estimates that are sensitive to the outcome of future events, actual results could differ from those estimates.

 

Recently Issued Accounting PronouncementsStock-Based Compensation

The Company considers the applicability and impact of all ASUs issued, both effective and not yet effective.

In May 2014, the FASB issued ASU 2014-09, “Revenue Recognition - Revenue from Contracts with Customers” (ASU 2014-09) that requires companies to recognize revenue when a customer obtains control rather than when companies have transferred substantially all risks and rewards of a good or service. This update is effective for annual reporting periods beginning on or after December 15, 2017 and interim periods therein and requires expanded disclosures. We have decided to adopt the guidance of Topic 606 now, commensurate with our first reported revenues from our primary product, so we will not have to make any changes in our revenue recognition process going forward.

In August 2014, FASB issued ASU 2014-15,Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern, or ASU 2014-15. ASU 2014-15 explicitly requires a company’s management to assess an entity’s ability to continue as a going concern, and to provide related footnote disclosures in certain circumstances. The new standard is effective in the first annual period ending after December 15, 2016. The adoption of this standard did not have a material impact on our condensed consolidated financial statements.

 

In April 2015, FASB issued ASU No. 2015-03, Interest – ImputationThe Company maintains a stock option incentive plan and accounts for stock-based compensation in accordance with ASC 718,Compensation - Stock Compensation. The Company recognizes share-based compensation expense, net of Interest (Subtopic 835-30): Simplifyingan estimated forfeiture rate, over the presentationrequisite service period of Debt Issuance Costs,the award to reduceemployees and directors. As required by fair value provisions of share-based compensation, employee and non-employee share-based compensation expense recognized is calculated over the complexityrequisite service period of having different balance sheet presentation requirementsthe awards and reduced for debt issuance costsestimated forfeitures.

Income Taxes

From inception to September 30, 2019, the Company has incurred net losses and, debt discountstherefore, has no current income tax liability. The net deferred tax asset generated by these losses is fully reserved as of September 30, 2019 and premiums.December 31, 2018, respectively, since it is currently likely that the benefit will not be realized in future periods.

As a result of the acquisition, the Company is required to file federal income tax returns and state income tax returns in the states of Arizona, Florida, Georgia, Minnesota, Pennsylvania, Tennessee, and Texas. There are no uncertain tax positions at September 30, 2019 or December 31, 2018. The guidance requires debt issuance costs related to a recognized debt liability be reportedCompany has not undergone any tax examinations since inception.

Net Loss Per Share

Basic loss per share is computed on the balance sheetbasis of the weighted average number of shares outstanding for the reporting period. Diluted loss per share is computed on the basis of the weighted average number of common shares plus dilutive potential common shares outstanding using the treasury stock method. Any potentially dilutive securities are antidilutive due to the Company’s net losses.

For the periods presented, there is no difference between the basic and diluted net loss per share: 32,756,181 warrants and 517,509 common stock options outstanding were considered anti-dilutive and excluded for the three and nine month periods ended September 30, 2019. For the nine month period ended September 30, 2018, there were no dilutive securities as a direct deduction from the carrying amount of that debt liability. ASU 2015-03 is effective for public companies for annual reporting periods beginning after December 15, 2015, and interim periods within those fiscal years.The Company adopted the amendments of ASU 2015-03 effective January 1, 2016. The adoption of this standardaccounting acquirer did not historically have a material impact on our condensed consolidated financial statements.

 -6-

In July 2015, the FASB issued ASU 2015-11, “Inventory (Topic 330),” which requires inventory measured using any method other than last-in, first-out or the retail inventory method to be subsequently measured at the lower of cost or net realizable value, rather than the lower of cost or market. ASU No. 2015-11 is effective for fiscal years beginning after December 15, 2016, including interim periods within those years. The Company adopted the amendments of ASU 2015-11 effective January 1, 2017. The adoption of this standard did not have a material impact on our condensed consolidated financial statements.

In November 2015, FASB issued ASU No. 2015-17, Balance Sheet Classification of Deferred Taxes. ASU 2015-17 simplifies the presentation of deferred taxes by requiring deferred tax assets and liabilities be classified as noncurrent on the balance sheet. ASU 2015-17 is effective for public companies for annual reporting periods beginning after December 15, 2016, and interim periods within those fiscal years. The adoption of this standard did not have a material impact on our condensed consolidated financial statements.

In February 2016, FASB issued ASU No. 2016-02, Leases (Topic 842). The core principle of Topic 842 is that a lessee should recognize the assets and liabilities that arise from leases. ASU 2016-02 is effective for public companies for annual reporting periods beginning after December 15, 2018, and interim periods within those fiscal years. The guidance may be adopted prospectively or retrospectively and early adoption is permitted. The Company is currently assessing the impact the adoption of ASU 2016-02 will have on its consolidated financial statements.stock compensation programs.

 

Note 3 – Accounts ReceivableBusiness Acquisition

 

Accounts receivable primarilyOn January 8, 2019, MedoveX completed its business combination with RMS under which MedoveX purchased certain assets and assumed certain liabilities of RMS, otherwise referred to as the Merger. Pursuant to the terms of the APA, MedoveX issued to the shareholders of RMS 33,661 shares plus 6,111 additional Exchange Shares (based on closing the sale of $2 million of new securities) for a total of 39,772 shares of Series C Preferred Stock where each share of Series C Preferred stock which automatically converted into 1,000 shares of common stock and represent amounts due from customersapproximately fifty-five percent (55%) of the outstanding voting shares of the Company.

Under the terms of the APA, the Company issued additional “Exchange Shares” to the shareholders of RMS to maintain the 55% ownership and not be diluted by the sale of convertible securities (“New Shares Sold”) until MedoveX raised an additional $5.65 million via the issuance of new securities. On the date of closing the Company issued 6,111 additional Exchange Shares to RMS Shareholders as a result of the issuance of additional securities, which are included in the 39,772 shares above. Subsequent to the closing of the purchase transaction, an incremental 11,153 additional Exchange Shares were issued, for which revenuea total of 17,264 additional Exchange Shares. All additional Exchange Shares have been issued to the shareholders of RMS and these Series C Preferred shares converted to 17,263,889 shares of common stock; no additional equity will be issued to RMS.

Because RMS shareholders owned approximately 55% of the voting stock of MedoveX after the transaction, RMS was deemed to be the acquiring company for accounting purposes (the “Acquirer”) and the transaction is accounted for as a reverse acquisition under the acquisition method of accounting for business combinations in accordance with U.S. GAAP. The assets acquired and the liabilities assumed of RMS included as part of the purchase transaction are recorded at historical cost. Accordingly, the assets and liabilities of MedoveX (the “Acquiree”) are recorded as of the Merger closing date at their estimated fair values.

Under the terms of the APA, MedoveX purchased certain assets and assumed certain liabilities of RMS. The assets of RMS reported on the MedoveX consolidated balance sheet as of December 31, 2018 that were excluded in the Merger on January 8, 2019 was cash of approximately $70,000. The Merger included the following: convertible debt to a related party of approximately $4,300,000, interest payable of approximately $158,000, accounts payable of approximately $224,000 and other current liabilities of approximately $285,000. Additionally, there were certain on-going litigation matters that were not assumed as part of the January 8, 2019 RMS reverse acquisition.

Purchase Price Allocation

The purchase price for the acquisition of the Acquiree has been recognized. Generally,allocated to the assets acquired and liabilities assumed based on their estimated fair values. The purchase price allocation herein is preliminary. The final purchase price allocation will be determined after completion of a thorough analysis to determine the fair value of all assets acquired and liabilities assumed but in no event later than one year following completion of the acquisition. Accordingly, the final acquisition accounting adjustments could differ materially from the allocation reflected as of September 30, 2019 presented herein. Any increase or decrease in the fair value of the assets acquired and liabilities assumed, as compared to the information shown herein, could also materially change the portion of purchase price allocated to goodwill and could materially impact the operating results of the Company doesfollowing the acquisition due to differences in purchase price allocation and depreciation and amortization related to some of these assets and liabilities.

The acquisition-date fair value of the consideration transferred is as follows:

Common shares issued and outstanding  24,717,271 
Common shares reserved for issuance upon conversion of the outstanding Series B Preferred Stock  2,312,500 
Total Common shares  27,029,771 
Closing price per share of MedoveX Common stock on January 8, 2019 $0.40 
   10,811,908 
Fair value of outstanding warrants and options  2,220,000 
Cash consideration to RMS  (350,000)
Total consideration $12,681,908 

Just prior to the transaction, MedoveX had 24.5 million shares of common stock outstanding at a market capitalization of $9.8 million. The estimated fair value of the net assets of MedoveX was $8.4 million as of January 8, 2019. Measuring the fair value of the net assets to be received by RMS was readily determinable based upon the underlying nature of the net assets. The fair value of the MedoveX common stock is above the fair value of its net assets. The MedoveX net asset value is primarily comprised of definite-lived intangibles as of the closing and the RMS interest in the merger is significantly related to obtaining access to the public market. Therefore, the fair value of the MedoveX stock price and market capitalization as of the closing date is considered to be the best indicator of the fair value and, therefore, the estimated purchase price consideration. During the three months ended September 30, 2019 the Company revised its purchase price allocation for the acquisition. As a result, the Company recorded a measurement period adjustment of $1,215,677 as an increase to goodwill adjusting the amount recorded as of January 8, 2019. The adjustment resulted in a corresponding increase to a derivative liability (see Note 12).

The following table summarizes the fair values of the assets acquired and liabilities assumed at the date of acquisition on January 8, 2019:

Cash $(302,710)
Accounts receivable  145,757 
Inventory  131,455 
Prepaid expenses  46,153 
Property and equipment  30,393 
Other  2,751 
Intangibles  3,680,000 
Goodwill  12,564,401 
Total assets acquired $16,298,200 
Accounts payable and other accrued liabilities  1,645,399 
Derivative liability  

1,215,677

 
Interest-bearing liabilities and other  755,216 
Net assets acquired $12,681,908 

Intangible assets are recorded as definite-lived assets and amortized over the estimated period of economic benefit. Goodwill is calculated as the difference between the acquisition-date fair value of the consideration transferred and the fair values of the assets acquired and liabilities assumed. Goodwill is not require collateralexpected to be deductible for income tax purposes. Goodwill is recorded as an indefinite-lived asset and is not amortized but tested for impairment on an annual basis or when indications of impairment exist.

Total interest bearing and other liabilities assumed are as follows:

Notes payable $99,017 
Short-term convertible notes payable  598,119 
Dividend payable  57,813 
Deferred rent  267 
Total interest-bearing and other liabilities $755,216 

Notes payable relate to promissory notes assumed by Acquiree in a 2015 acquisition, which was later divested in 2016, with the assumed promissory notes being retained by Acquiree. The Company finalized an eighteen-month extension on the notes extending the maturity date to March 1, 2021. Payments on both of the notes are due in aggregate monthly installments of approximately $5,800 and carry an interest rate of 5%. The promissory notes had outstanding balances of $95,000 as of September 30, 2019. The promissory notes had outstanding balances of approximately $99,000 plus accrued interest of approximately $3,000 at January 8, 2019 (see Note 11).

In the third quarter of 2018, convertible notes were issued pursuant to a securities purchase agreement with select accredited investors, whereby the Acquiree offered up to 1,000,000 units (the “Units”) at a purchase price of $50,000 per Unit. Each Unit consisted of (i) a 12% senior secured convertible note, initially convertible into shares of the Company’s common stock, par value $0.001 per share, at a conversion price equal to the lesser of $0.40 or ninety percent (90%) of the per share purchase price of any other securityshares of common stock or common stock equivalents issued in future private placements of equity and/or debt securities completed by the Company following this offering of Units, and (ii) a three-year warrant to supportpurchase such number of shares of the Company’s common stock equal to one hundred percent (100%) of the number of shares of common stock issuable upon conversion of the notes at $0.40. The warrants are exercisable at a price equal to the lesser of $0.75 or ninety percent (90%) of the per share purchase price of any shares of common stock or common stock equivalents issued in future private placements of the debt and/or equity securities completed by the Company following the issuance of warrants. As a result of the price adjustment feature, the conversion price of the convertible notes was adjusted to $0.36 per share.

In the offering, the Acquiree sold an aggregate of 15 Units and issued to investors an aggregate of $750,000 in principal amount of convertible notes and 1,875,000 warrants to purchase common stock, resulting in total gross proceeds of $750,000 to the Company. If converted at $0.40 the convertible notes sold in the offering are convertible into an aggregate of 1,875,000 shares of common stock. Due to the notes maturing during the third quarter of 2019, the warrants have fully accreted as of September 30, 2019. The Acquiree recorded the proceeds from the notes and the accompanying warrants, which accrete over the period the notes are outstanding, on a relative fair value basis of approximately $505,000 and $245,000, respectively. At acquisition date, the value of the notes was approximately $598,000.

The convertible notes had maturity dates between August and September 2019 and were renegotiated during the third quarter of 2019 (see Note 11).

The following schedule represents the amounts of revenue and net loss attributable to the MedoveX acquisition which have been included in the consolidated statements of operations for the periods subsequent to the acquisition date:

  Three Months Ended  Nine Months Ended 
  September 30, 2019  September 30, 2019 
Revenues $28,405  $63,910 
Net loss attributable to MedoveX  (7,203)  (1,956,705)

The following unaudited pro forma financial information represents the consolidated financial information as if the acquisition had been included in the consolidated results beginning on the first day of the fiscal year prior to its receivables.acquisition date. The pro forma results have been calculated after adjusting the results of the acquired entity to remove any intercompany transactions and transaction costs incurred and to reflect any additional depreciation and amortization that would have been charged assuming the fair value adjustments to property and equipment and intangible assets had been applied on the first day of the fiscal year prior to its acquisition date, together with the consequential tax effects. The pro forma results do not reflect any cost savings, operating synergies or revenue enhancements that the combined entities may achieve as a result of the acquisition; the costs to combine the companies’ operations; or the costs necessary to achieve these cost savings, operating synergies or revenue enhancements. The pro forma results do not necessarily reflect the actual results of operations of the combined companies under the current ownership and operation.

  For the Three Months Ended September 30, 2018 
  RMS  MedoveX  Pro Forma 
Revenues $1,536,990  $206,159  $1,743,149 
Net loss  (1,035,251)  (1,382,275)  (2,417,526)
Net loss attributable to common shareholders  (1,035,251)  (1,512,326)  (2,547,577)
             
Loss per share- basic and diluted $(0.03) $(0.06) $(0.04)

  For the Nine Months Ended September 30, 2018 
  RMS  MedoveX  Pro Forma 
Revenues $6,880,794  $598,773  $7,479,567 
Net loss  (2,295,173)  (3,721,958)  (6,017,131)
Net loss attributable to common shareholders  (2,295,173)  (4,119,068)  (6,414,241)
             
Loss per share- basic and diluted $(0.07) $(0.18) $(0.11)

 

Note 4 – Other Receivables

Other receivables include input and importation value added tax (VAT) paid by the Company for conducting business in the European Union (“EU”) and for importing goods from outside the EU.

Note 5 - Inventory

 

Inventories consistInventory consists only of finished goods and areis valued at the lower of cost or net realizable value, using the first-in, first-out (FIFO) method. Inventories were acquired in the Merger and therefore there were no inventories prior to January 8, 2019.

 

InventoriesInventory consisted solely of the following items asPro-40 Generators totaling approximately $126,000 and $0 at September 30, 2019 and December 31, 2018, respectively.

Note 5 – Right-of-use Asset And Lease Liability

Upon adoption of ASU No. 2016-02 (as amended) (See Note 2), additional current liabilities of approximately $475,000 and long-term liabilities of approximately $713,000 with corresponding ROU assets of approximately $1,167,000 were recognized, based on the present value of the remaining minimum rental payments under the new leasing standards for existing operating leases.

The unaudited consolidated balance sheet at September 30, 2019 reflects current lease liabilities of approximately $481,000 and long-term liabilities of $396,000, with corresponding ROU assets of $859,000.

Operating lease expense and cash flows from operating leases for the three and nine months ending September 30, 2019 totaled approximately $140,000 and $389,000, respectively, and are included in the “Other general and administrative” section of the unaudited consolidated statement of operations.

The Company leases corporate office space in Tampa, FL and Atlanta, GA. The Company also leases medical clinic space in Tampa, FL, Nashville, TN, Scottsdale, AZ, Pittsburgh, PA, and Dallas, TX. The leasing arrangements contain various renewal options that are adjusted for increases in the consumer price index or agreed upon rates. Each location has its own expiration date ranging from April 30, 2020 to August 31, 2023. The Company expects to renew each lease upon expiration in order to continue operations.

As of September 30, 2017, and December 31, 2016:2019, the undiscounted minimum future maturities of lease liabilities are as follows:

 

  September 30, 2017  December 31, 2016 
Split Return Electrodes $334  $ 
Denervex device  29,533    
Pro-40 generator  

135,000

    
Total $

164,867

  $ 
Remainder of 2019 $138,000 
2020  482,000 
2021  155,000 
2022  103,000 
2023  69,000 
  $947,000 

 

Note 6 - Property andAnd Equipment

 

Property and equipment, net, consists of the following:

 

 Useful Life September 30, 2017 December 31, 2016  Useful Life September 30, 2019 December 31, 2018 
Furniture and fixtures 5 years $67,777  $65,987  5-7 years $147,870  $149,285 
Computers and software 3 years  29,866   19,928  3-7 years  361,986   278,234 
Leasehold improvements 5 years  35,673   32,593  15 years  157,107   156,133 
    133,316   118,508     666,963   583,652 
Less accumulated depreciation    (40,918)  (20,918)    (431,738)  (316,736)
                    
Total   $92,398  $97,590    $235,225  $266,916 

 

Depreciation expense amounted to $7,109was approximately $28,000 and $20,000,$80,000, respectively, for the three and nine months ended September 30, 2017.2019. Depreciation expense was approximately $35,000 and amortization expense, excluding depreciation and amortization from Streamline, amounted to $2,033 and $6,042,$84,000, respectively, for the three and nine months ended September 30, 2016.2018.

 

Note 7 - Intangible Assets

As of September 30, 2019, intangible assets acquired as part of the Merger, net of accumulated amortization of $552,000, totaled approximately $3,128,000. Amortization expense was $184,000 and $552,000 for the three and nine months ended September 30, 2019.

The following is a schedule of expected future amortization of intangible assets as of September 30, 2019:

Remainder of 2019 $184,000 
2020  736,000 
2021  736,000 
2022  736,000 
2023  736,000 
Total $3,128,000 

Note 8 – Related Party Transactions

Consulting Expense

The Company entered into an oral consulting agreement with Mr. Raymond Monteleone, Board Member and Chairman of the Audit Committee, in which Mr. Monteleone receives $10,000 per month for advisory services and $5,000 per quarter as Audit Committee Chair in addition to regular quarterly board meeting fees. This arrangement has no specified termination date. For the three and nine months ended September 30, 2019, the Company has expensed approximately $35,000 and $90,000 in compensation to Mr. Monteleone, respectively.

Board Member Expenses

For the three and nine months ended September 30, 2019, the Company paid $0 and $5,000 each for Board of Director fees to Michael Yurkowsky and to Raymond Monteleone for a total of $0 and $10,000, respectively.

Debt and Other Obligations

The Company had various related party transactions in 2018. For the period of January 1, 2018 to March 13, 2018, the Company received $528,175 from one of its shareholders (RMS members) and $228,175 from its CEO (RMS CEO) as part of a line of credit that was established in 2017. On March 13, 2018, the entire $1,856,350 line of credit received from the Member and the CEO, including contributions from 2017, was transferred to the BioCell Capital, LLC debt instrument, (“BioCell Capital Line of Credit”).

The BioCell Capital Line of Credit also consisted of capital contributions from related parties totaling approximately $4,306,000, inclusive of the aforementioned $1,856,300, to RMS in 2018. The BioCell Capital Line of Credit was converted to RMS members’ equity and was excluded from the APA on January 8, 2019.

The Company also received a short-term advance from one of its shareholders (RMS members), who was also the CEO of H-CYTE, in the amount of $180,000 in December 2018 for working capital needs. Approximately $66,000 of the advance was repaid in January 2019 and approximately $114,000 was converted to equity as part of the APA on January 8, 2019.

Horne Management, LLC, controlled by Chief Executive Officer, William E. Horne, advanced funds for operations totaling $900,000 on July 25, 2019. These loans accrue interest at 5.5% and are due and payable upon demand of the creditor.

In addition, Horne Management, LLC loaned H-CYTE $350,000 on September 26, 2019, for working capital purposes. The terms of the loan as follows:

  -7-12% interest rate with a maturity date of March 26, 2020.
 If the Company does not pay back the principal and interest by November 26, 2019, the Company shall issue to Lender a three-year warrant to purchase 400,000 shares of the Company’s common stock with a purchase price of $0.75 per share.
If the Company is unable to pay the loan as of March 26, 2020, the interest rate increases to 15%.

 

Note 79 - Equity Transactions

 

For the consolidated statements of stockholders’ equity (deficit) as of December 31, 2018, the common stock, preferred stock and additional paid in capital reflect the accounting for the stock received by the RMS members as of the Merger as if it was received as of the beginning of the periods presented and the historical accumulated deficit of RMS. As of the closing of the Merger, before the contingent additional exchange shares impact from the sale of new securities, the stock received by RMS was 33,661 shares of Series C Preferred Stock, which was later converted into approximately 33,661,000 shares of common stock, with common stock par value of approximately $33,700 and additional paid-in capital of approximately $3,566,000. The historical accumulated deficit of RMS as of the closing was approximately $9,296,000.

Common stock issuanceStock Issuance

 

In November 2016,On January 8, 2019, the Company entered into a securities purchase agreement (the “SPA”) with four purchasers (the “Purchasers”) pursuant to which the four Purchasers invested in the Company an aggregate amount of $2,000,000, with $1,800,000 in cash and $200,000 by cancellation of debt as explained below, in exchange for forty (40) units (the “Units”), each consisting of a convertible note (the “Convertible Note”) with the principal amount of $50,000 and a warrant (the “Warrant”) to purchase common stock (the “common stock”) of the Company at a purchase price of $.075 per share. Pursuant to this SPA, the Company initially offered a minimum of $1,000,000 and a maximum of $6,000,000 Units, and subsequently increased the maximum amount to $8,000,000 (the “Maximum Amount”) of Units at a price of $50,000 per Unit until the earlier of i) the closing of the subscription of the Maximum Amount and ii) March 31, 2019 (the “Termination Date”), subject to the Company’s earlier termination at its discretion. The SPA includes the customary representations and warranties from the Company and purchasers. Steve Gorlin, the Company’s former Chairman of the Board, authorizedconverted a $200,000 promissory note owed to him by the issuanceCompany in exchange for four (4) Units on the same terms as all other Purchasers. Mr. Gorlin subsequently converted the promissory note underlying the Units into an aggregate of 500,000 shares of common stock, eliminating the Company’s debt obligation.

Each Convertible Note had an interest rate of 12% per annum, a principal amount of $50,000 maturity date of January 8, 2020, and will be convertible into shares of common stock at a price of $0.40 subject to adjustment as provided for in the Convertible Note. Pursuant to the terms of the Convertible Note, each holder of the Convertible Note shall not own more than 4.99% of the number of shares of common stock outstanding immediately after giving effect to the issuance of common stock issuable upon exercise of such Convertible Note. If defaulted, the penalty interest rate of the Convertible Note shall rise to 18% per annum. In addition, each Warrant is exercisable at a price of $0.75 per share (the “Exercise Price”), subject to adjustments stated therein. The holder of each Warrant may purchase the number of shares of common stock equal to the number of shares of common stock issuable upon conversion of each Convertible Note while the Warrant is exercisable. The Warrants have a term of three years and shall be exercised in cash or on a cashless basis as described in the Warrant agreement. All Convertible Notes have been converted into an aggregate of 18,000,000 shares of common stock.

As reported on Form 8-K filings on January 25, 2019, February 8, 2019, March 15, 2019 and April 5, 2019, the Company entered into other SPA’s with additional purchasers, which brought the aggregate amount of capital raised in all Board members, both current and former, in an amount equivalentthese offerings to $240,000, representing their accrued but unpaid directors’ fees$7,200,000, as of December 31, 2016. that latest date.

As a result of the sales of new securities of at least $5,650,000, the Company issued an additional 17,264 Series C Preferred Stock which automatically converted to 17,263,889 shares of common stock.

All the Convertible Notes from the SPA, as well as the shares of Series C Preferred Stock issued to RMS members, were automatically converted into shares of common stock.

The foregoing description of the SPA, Convertible Note, and Warrant is qualified in its entirety by reference to the respective agreements.

In January 2017,February 2019, 250,000 shares of common stock were issued pursuant to conversion of short-term debt and accrued interest.

In March 2019, the Company issued an aggregate of 173,911130,085 shares of common stock at $1.38$0.40 per share for consulting fees in an amount equivalent to $52,034.

On April 25, 2019, the Company issued 4,225,634 shares of common stock valued at $0.40 per share to Mr. William E. Horne, the Company’s CEO, in a restricted stock award which was 100% vested when issued. The Company recognized approximately $1,690,000 of compensation expense in the average closing pricequarter ended June 30, 2019 related to the restricted stock award. This restricted stock award was issued pursuant to his employment agreement with the Company, which stated that this restricted stock award  (as well as the incentive stock options issued in the quarter ended March 31, 2019) would be fully vested if not issued within fifteen days of the Merger. Neither award was issued within that time frame and both awards became fully vested when issued. The aggregate number of shares of common stock from these two awards is 4,475,634 and was calculated based on 7% of the Company’s issued and outstanding common stock during 2016, to fulfill this obligation. Theas of the closing of the Merger.

During the third quarter of 2019, the Company raised $100,000 by selling 200,000 shares of common stock at $0.50 per share. They also issued the investors 100,000 warrants with an exercise price of the Company’s stock on January 17, 2017, the day the shares were issued, was $1.16$1.00 per share.

 

In August 2017, the Board authorizedthird quarter of 2019, the issuance ofCompany issued 150,000 shares of common stock to all Board members, both currenta consultant in consideration of consulting services rendered to the Company. At the time of issuance, the fair market value of the shares was $0.29, and, former,as a result, $43,500 was expensed in an amount equivalent to $135,000, representing their accrued but unpaid directors’ fees as ofthe three and nine months ended September 30, 2017. In October 2017, the Company issued an aggregate of 115,389 shares at $1.17 per share, which was the average closing price of the Company’s stock through September 30, 2017, to fulfill this obligation. The closing price of the Company’s stock on October 30, 2017, the day the shares were issued, was $1.09 per share. See Note 17.2019.

 

Stock-Based Compensation Plan

2013 Stock Option Incentive Plan

During the nine months ended September 30, 2017,2019, 636,480 shares were issued pursuant to conversions of some of our Series B Convertible Preferred Stock (“Stock B Preferred”) and accrued dividends thereunder.

Series B Preferred Stock Preferences

Voting Rights

Holders of our Series B Preferred Stock (“Series B Holders”) have the Boardright to receive notice of Directors authorizedany meeting of holders of common stock or Series B Preferred Stock and to vote upon any matter submitted to a vote of the holders of common stock or Series B Preferred Stock. Each Series B Holder shall vote on each matter submitted to them with the holders of common stock.

Liquidation

Upon the liquidation, dissolution or winding up of the business of the Company, whether voluntary or involuntary, each Series B Holder shall be entitled to issue optionsreceive, for each share thereof, out of assets of the Company legally available therefore, a preferential amount in cash equal to purchasethe stated value plus all accrued and unpaid dividends. All preferential amounts to be paid to the Series B Holders in connection with such liquidation, dissolution or winding up shall be paid before the payment or setting apart for payment of any amount for, or the distribution of any assets of the Company’s to the holders of the Company’s common stock. The Company accrues these dividends as they are earned each period.

On January 8, 2019, the Company completed the issuance of Convertible Notes with a conversion price of $0.40. As a result, the exercise price on all of the warrants issued with the Series B Preferred Stock was adjusted downward to 90% of that conversion price, or $0.36.

The Company recognized a beneficial conversion feature related to the Series B Preferred Stock of approximately $33,000, which was credited to additional paid-in capital, and reduced the income available to common shareholders. Because the Series B Preferred Stock can immediately be converted by the holder, the beneficial conversion feature was immediately accreted and recognized as a deemed dividend to the preferred shareholders.

Series B preferred Stock Conversions

During the nine months ended September 30, 2019, 9,250 shares of Series B Preferred Stock, par value $0.001, and accrued dividends were assumed with the Merger and an aggregate of 189,1592,250 shares of Series B Preferred Stock, and accrued dividends, were subsequently converted into an aggregate of 604,167 shares of the Company’s common stock.

Debt Conversion

Convertible Notes

The $750,000 convertible notes payable assumed in the Merger had a fair value of approximately $598,000 on the acquisition date. Subsequently, on February 6, 2019, $100,000 of the outstanding Convertible Notes was converted into an aggregate of 250,000 shares of common stock, to certain employees. The stock options vest as follows: 25% on date of grant and 25% on eacheliminating $100,000 of the next three years afterCompany’s debt obligation. The debt was converted into shares of common stock at $0.40 per share, in accordance with the grant date. The options granted were atSPA.

In connection with the market valueAPA, on January 8, 2019, Steve Gorlin, the Company’s former Chairman of the Board, converted a $200,000 promissory note owed to him by the Company pursuant to the same terms of the SPA entered into by other investors to consummate the acquisition on January 8, 2019. The promissory note was converted into an aggregate of 500,000 shares of common stock, oneliminating the date of the grant.Company’s debt obligation.

Stock-Based Compensation Plan

 

We utilize2013Stock Option Incentive Plan

The Company utilizes the Black-Scholes valuation method to recognize stock-based compensation expense over the vesting period. The expected life represents the period that ourthe stock-based compensation awards are expected to be outstanding.

 

We use a simplified method provided in SecuritiesIncluding the expense of approximately $1,690,000 related to the restricted stock award to the Company’s CEO, total stock-based compensation expense for the three and Exchange Commission release,Staff Accounting Bulletin No. 110,nine months ended September 30, 2019 was approximately $1,473 and $1,786,500, respectively. The nine months ended September 30, 2019 includes $1,690,000 of compensation expense related to the Company’s CEO restricted stock award which averages an award’s weighted average vesting period and contractual term for “plain vanilla” share options. The expected volatility was estimated by analyzing100% vested when issued. This restricted stock award was issued pursuant to his employment agreement with the historic volatility of similar public biotech companies in an early stage of development. No dividend payouts were assumed as we haveCompany, which stated that this option grant would be fully vested if not historically paid, and do not anticipate paying, dividends in the foreseeable future. The risk-free rate of return reflects the weighted average interest rate offered for US treasury rates over the expected termissued within fifteen days of the options.reverse merger transaction. The restricted stock award was not issued within that time frame and was fully vested when issued.

 

The significant assumptions used to estimate the fair value of the equity awards granted are:Stock Option Activity

Grant date  February 3   March 28 
Fair value of options granted $0.7992  $0.9114 
Expected term (years)  6   6 
Risk-free interest rate  2.10%  2.11%
Volatility  82.53%  76.86%
Dividend yield  None   None 

 

For the three and nine months ended September 30, 2017,2019, the Company recognized approximately $111,000$1,500 and $612,000,$94,000, respectively, as compensation expense with respect to vested stock options. ForNo compensation expense was recorded prior to the three andMerger. Since these stock options were assumed on January 8, 2019 as part of the Merger, there were no historical costs related to this prior to January 8, 2019. The expense for the nine months ended September 30, 2016,2019 is primarily related to a fully-vested option to purchase 250,000 shares of the Company recognized approximately $230,000Company’s common stock that was issued to the Company’s CEO pursuant to his employment agreement, which stated that this option grant would be fully vested if it was not issued within fifteen days of the Merger. The option was not granted within that time frame and $562,000, respectively, as compensation expense with respect to stock options.was fully vested when issued.

 

Stock Option Activity

As of September 30, 2017,2019, there were 374,3199,501 shares of time-based, non-vestedunvested stock options outstanding. As of September 30, 2017, there wasand unrecognized compensation expense totaled approximately $298,000 of total unrecognized stock-based compensation related to these non-vested stock options. That$2,400. The remaining expense is expected towill be recognized as an expense on a straight-line basis over a remaining weighted average period of 1.84 years.service period.

 

The following is a summary of stock option activity atfor the nine months ending September 30, 2017:2019:

 

  Shares  Weighted
Average
Exercise
Price
  Weighted
Average
Remaining Term
(Years)
 
Outstanding at 12/31/2016  1,124,900  $2.15   9.0 
             
Granted  189,159  $1.15   9.37 
Outstanding at 9/30/2017  1,314,059  $2.01   8.45 
Exercisable at 9/30/2017  939,740  $2.09   8.37 
  Shares  Weighted
Average
Exercise
Price
  Weighted
Average
Remaining
Term
(Years)
 
Outstanding at December 31, 2018    $    
             
Assumed with the RMS merger transaction  557,282  $2.78   6.06 
Other activity since January 8, 2019:            
Granted  250,000  $0.40   9.27 
Cancelled  (289,774) $2.46    
Outstanding at September 30, 2019  517,508  $1.81   7.62 
Exercisable at September 30, 2019  508,007  $1.81   7.62 

 

 -8-

Note 10 – Commitments & Contingencies

 

Private PlacementBiotechnology Agreement

 

On February 9, 2017,June 21, 2019, the Company entered into a Unit Purchase Agreement10-year exclusive and extendable product supply agreement with selected accredited investors wherebyRion that will enhance its existing cytotherapy product line, developing a disruptive technology for COPD, the Company hadfourth leading cause of death in the rightU.S. Rion has established a unique exosome technology to sell in a private placement a minimum of $3,000,000 and up to a maximum of $5,000,000 of units. Each Unit had a purchase price of $100,000 and consisted of (i) 96,154 sharesharness the healing power of the Company’s common stock, par value $0.001 per sharebody. Rion’s novel exosome technology, based on science developed at Mayo Clinic, provides an off-the-shelf platform to enhance healing in soft tissue, musculoskeletal, cardiovascular and neurological organ systems. With this agreement, Rion will serve as the product supplier and will co-develop a purchase priceproprietary cellular platform with H-CYTE for the treatment of $1.04 per share,COPD. H-CYTE will control the commercial development and (ii) a warrantfacilitate clinical trial investigation. After conducting joint research and development of these biologics, H-CYTE intends to purchase 48,077 sharespursue submission of common stock. Each warrant has an initial exercise priceinvestigational new drug (IND) application for review by the FDA for treatment of $1.50 per share and is exercisable for a period of five (5) years from the date of issuance. Investors had the option to request shares of the Company’s Series A Convertible Preferred Stock (the “Series A Preferred Stock”) in lieu of common stock, on a basis of one share of preferred stock for every one hundred shares of common stock.COPD.

Sublease Agreement

 

The offering resulted in gross proceeds of $3,022,000 and resulted in the issuance of an aggregate of 1,631,730 shares of common stock, 12,740 shares of Series A Preferred Stock and warrants to purchase 2,005,761 shares of common stock. The placement agent collected an aggregate of approximately $350,000 in total fees related to the offering and warrants to purchase an aggregate of 405,577 shares of common stock at a price of $1.50 per share.

Each share of Series A Preferred Stock may be converted into shares of fully paid and non-assessable shares of common stock at a rate of one hundred shares of the Company’s common stock for every share of Series A Preferred Stock.

On July 14, 2017, the Company entered into a Securities Purchase Agreement with selected accredited investors wherebysub-lease agreement for the lease in Alpharetta, Georgia. The period of the lease is from July 1, 2019 to December 31, 2020 and sublessee shall pay to sublessor a minimum rent, of $2,000 per month recognized by the Company sold an aggregate of 2,956,043 shares of common stock and 1,478,022 warrants to purchase common stock. The Offering resulted in $2,469,000 in net proceeds to the Company. The common stock shares were sold at $0.91 per share which was the closing price of the Company’s common stock on July 13, 2017, the day prior to the agreement. Each warrant has an exercise price of $1.15 and is exercisable for a period of five years commencing six months from the date of issuance.as rental income.

 

Debt ConversionConsulting Agreements

 

On February 9, 2017, the Company’s $1,150,000 short-term note payable was converted into an aggregate of 165,865 shares of common stockThe Company has reached a new agreement with Jesse Crowne, a former Director and 9,399 shares of Series A Preferred Stock, eliminating the Company’s debt obligation. The debt was converted into shares at $1.04 per share, which was the offering priceCo-Chairman of the Company’s stock in the February private placement. Each share of Series A Preferred Stock may be converted into shares of fully paid and non-assessable shares of common stock at a rate of one hundred sharesBoard of the Company’s common stockCompany, to provide business development consulting services for every sharea fee of Series A Preferred Stock.

As consideration for converting the debt, the noteholders’ agreed to receive common stock in lieu of the 200,000 warrants to purchase common stock that were issued in conjunction with the short-term loan. See Note 10.

As a result, the 200,000 warrants were cancelled, and the Company issued to the noteholders’ an aggregate of 200,000 shares of common stock. The closing price of the Company’s stock on February 9, 2017, the day the shares were issued, was $1.04$5,000 per share. The fair value of the common stock issued was approximately $208,000.

preferred Stock Conversion

On March 31, 2017, 4,147 shares of Series A Preferred Stock were converted into an aggregate of 414,663 restricted shares of authorized common stock, par value $0.001 per share.

On April 21, 2017, 5,252 shares of Series A Preferred Stock were converted into an aggregate of 525,240 restricted shares of authorized common stock, par value $0.001 per share.

Note 8 - Commitments

Operating Leases

Office Space

month. The Company pays TAG Aviation, a company owned by its Chief Executive Officer, Jarrett Gorlin (“Mr. Gorlin”) for office space that is currently being used as the Company’s principal business location plus utilities cost (see “Related Party Transactions”) on a monthly basis. Base annual rent is $2,147 per month. Rentincurred expense of approximately $10,000 and utilities cost paid to TAG Aviation amounted to approximately $9,500 and $25,000$50,000, for the three and nine months ended September 30, 2017, respectively. Rent expense2019, respectively, related to this consulting agreement. Since this agreement was assumed on January 8, 2019 as part of the Merger, there were no historical costs related to this prior to January 8, 2019.

The Company entered into a consulting agreement with LilyCon Investments, LLC effective February 1, 2019 for services related to evaluation and utilities costnegotiation of future acquisitions, joint ventures, and site evaluations/lease considerations. The duration of the consulting agreement is for a period of twelve months in the amount of $12,500 per month with a $15,000 signing bonus which was paid in full during the quarter ending March 31, 2019. The agreement also provides LilyCon Investments with $35,000 in stock (to be calculated using an annual Variable Weighted Average Price from February 2019 through January 2020) to TAG Aviation amountedbe granted on the one-year anniversary of this agreement, if the agreement has not been terminated prior to approximately $7,000 and $21,000 forthat date. Either party may terminate this agreement with or without cause upon 30 days written notice. For the three and nine months ended September 30, 2016,2019, the Company expensed a total of $37,500 and $115,000 in compensation to LilyCon Investments, respectively.

 

On July 8, 2015, theThe Company entered into a 3-year leasean oral consulting arrangement with St. Louis Family Office, LLC, controlled by Jimmy St. Louis, former CEO of RMS, in January 2019 in the amount of $10,000 per month plus benefits reimbursement for advisory services. The Company terminated this agreement for a commercial building which commenced on August 1, 2015. Base rent foreffective June 30, 2019. For the three and nine months ended September 30, 2017 was $2,849 per month. Total lease expense2019, the Company expensed $0 and $71,000 in consulting fees to St. Louis Family Office, respectively.

The Company entered into a consulting agreement with Strategos Public Affairs, LLC (Strategos) on February 15, 2019 for a period of twelve months, unless otherwise terminated by giving thirty days prior written notice. Strategos will provide information to key policymakers in the legislature and executive branches of government on the benefits of the cellular therapies offered by the Lung Health Institute, advocate for legislation that supports policies beneficial to patient access and oppose any legislation that negatively impacts the Company’s ability to expand treatment opportunities, and position the Company and its related entities as the expert for information and testimony. For the three and nine months ended September 30, 2017 was approximately $8,6002019, the Company expensed $22,500 and $26,000, respectively,$48,500, respectively.

The Company entered into a consulting agreement with Goldin Solutions, effective August 4, 2019, for media engagement and related to this lease. Total lease expense forefforts, including both proactive public relations and crisis management services. The agreement has a minimum term of six months, with a $33,000 monthly fee payable each month, with the exception of a first month discount of $12,000. For the three and nine months ended September 30, 2016 was approximately $8,300 and $25,000, respectively, related to this lease.

 -9-

Future minimum lease payments under this rental agreement are approximately as follows:

For the year ending:

December 31, 2017 $8,900 
December 31, 2018  21,000 
  $29,900 

Equipment

The Company entered into a non-cancelable 36-month operating lease agreement for equipment on April 22, 2015. The agreement is renewable at the end of the term and requires2019, the Company to maintain comprehensive liability insurance. Total lease expense was approximately $900 and $2,900, respectively, for the three and nine months ended September 30, 2017. Total lease expense was approximately $900 and $2,500, respectively, for the three and nine months ended September 30, 2016.expensed $54,000.

 

Future minimum lease payments under this operating lease agreement are approximately as follows:

For the year ending:

December 31, 2017 $700 
December 31, 2018  800 
  $1,500 

Consulting Agreements

In January 2017, the consulting agreement with one of the Company’s founding stockholders to provide business development consulting services was modified from $5,000 per month to $10,000 per month and extended through January 2018. The Company paid $30,000 and $85,000, respectively, for the three and nine months ended September 30, 2017 under this new arrangement. The Company paid $15,000 and $40,000, respectively, for the three and nine months ended September 30, 2016 under the previous arrangement.

On August 23, 2017, the Company retained a consulting firm to provide advisory services specific on matters with respect to potential mergers and acquisitions over a nine-month period at a fee of $75,000. The fee is payable in quarterly installments of $25,000 beginning at the start of the advisory period and every three months thereafter. The engagement terminates on May 10, 2018. No amounts were due or paid at September 30, 2017 per the terms of the agreement.

In July 2017, the Company modified the consulting agreement with the sales, marketing, and distribution consultant in Latin America. The agreement to provide consulting services was modified from $5,000 per month to $7,000 per month and extended through December 31, 2017. The Company paid $21,000 and $45,000, respectively, for the three and nine months ended September 30, 2017.

The Company has consulting agreements with three sales, marketing, and distribution consultants in Europe who provide consulting services for aggregate compensation amounting to approximately €27,500 per month. The consulting agreements, while subject to modifications, commenced at separate dates and will also terminate at separate dates through April 30, 2019. The Company paid approximately $58,000 and $131,000, respectively, for the three and nine months ended September 30, 2017. The Company paid approximately $25,000 and $46,000, respectively, for the three and nine months ended September 30, 2016.

Employment Agreements

The Company has Employment Agreements with each of its six executive officers for aggregate compensation amounting to approximately $1,064,000 per annum, plus customary benefits. These employment agreements, having commenced at separate dates, are for terms of three years which began in October 2013 and end in January 2018.

Generator development agreement

The Company is obligated to reimburse Bovie up to $295,000 for the development of the Pro-40 electrocautery generator. The Company paid approximately $3,000 and $33,000, respectively, for the three and nine months ended September 30, 2017 under this agreement. The Company paid approximately $1,000 and $24,000, respectively, for the three and nine months ended September 30, 2016 under this agreement. Through September 30, 2017, we have paid approximately $422,000 to Bovie related to this agreement.

 -10-

Distribution center and logistic services agreement

 

The Company has a non-exclusive distribution center agreement with a logistics service provider in Berlin, Germany pursuant to which they shall manage and coordinate the DenerveX System products which the Company exports to the EU through June 2019.2020 The Company payspaid a fixed monthly fee of €2,900€4,500 (approximately $5,000) for all accounting, customs declarations and office support, and a variable monthly fee ranging from €1,900 to €6,900 (approximately $2,300 to $8,300), based off volume of shipments, for logistics, warehousing and customer support services.

Total expenses paidincurred for the distribution center and logistics agreement waswere approximately $37,900$10,080 and $37,900,$40,080, respectively, for the three and nine months ended September 30, 2017.2019. Since this agreement was assumed on January 8, 2019 as part of the reverse merger transaction, there were no historical costs related to this prior to January 8, 2019.

Patent Assignment and Contribution Agreements

The terms of a Contribution and Royalty Agreement dated January 31, 2013 with Dr. Scott Haufe, M.D was assumed in the Merger as of January 8, 2019. This agreement provides for the Company to pay Dr. Haufe royalties equal to 1% of revenues earned from sales of any and all products derived from the use of the DenerveX technology. Royalties are payable to Dr. Haufe within 30 days after the close of each calendar quarter based on actual cash collected from sales of applicable products. The royalty period expires on September 6, 2030.

The Company incurred approximately $0 and $1,100 respectively, in royalty expense under the Contribution and Royalty agreement for the three months and nine months ended September 30, 2019, all of which was included in accounts payable at September 30, 2019. Since this agreement was assumed on January 8, 2019 as part of the Merger, there were no historical costs related to this prior to January 8, 2019.

Litigation

From time to time, the Company may be involved in routine legal proceedings, as well as demands, claims and threatened litigation that arise in the normal course of our business. The ultimate amount of liability, if any, for any claims of any type (either alone or in the aggregate) may materially and adversely affect the Company’s financial condition, results of operations and liquidity. In addition, the ultimate outcome of any litigation is uncertain. Any outcome, whether favorable or unfavorable, may materially and adversely affect the Company due to legal costs and expenses, diversion of management attention and other factors. The Company expenses legal costs in the period incurred. The Company cannot assure that additional contingencies of a legal nature or contingencies having legal aspects will not be asserted against the Company in the future, and these matters could relate to prior, current or future transactions or events.

Guarantee

The Company has guaranteed payments based upon the terms found in the management services agreements to two affiliated physicians related to LI Nashville, LI Scottsdale, LI Pittsburgh, and LI Dallas. For the three and nine months ending September 30, 2019, payments totaling approximately $42,000 and $105,000 respectively were made to these affiliates.

 

Note 911Short Term LiabilitiesShort-term Debt

 

Finance Agreement

The Company entered into a commercial insurance premium finance and security agreement in December 2016. The agreement finances the Company’s annual D&O insurance premium. Payments are due in quarterly installments of approximately $23,000 and carry an annual percentage interest rate of 4.9%.

The Company had paid the yearly premium in full and had no outstanding balance at September 30, 2017 related to the agreement.

Promissory Notes Payable

 

In conjunction with the consummation of the Streamline acquisition on March 25, 2015, the Company assumedShort-term financing payable relates to financing arrangements for Directors and Officers and general liability insurance premiums that were financed at various points throughout 2018 and 2019 and two promissory notes assumed in the merger transaction.

These financing arrangements require aggregate monthly payments of approximately $18,000, with interest rates ranging from 7% to 12.8% and are to be paid in full by July 2020. The financing arrangements had balances of approximately $114,000 at September 30, 2019 and $31,000 at December 31, 2018. Interest expense related to these arrangements was approximately $2,000 and $4,300 for approximately $135,000the three and $125,000 tonine months ended September 30, 2019, respectively, and was $0 for the Bank of North Dakota New Venture Capital Programthree and North Dakota Development Fund, both outside non-related parties. Payments on bothnine months ended September 30, 2018 respectively.

Two promissory notes payable assumed in the Merger are due in aggregate monthly installments of approximately $5,700 and carry an interest rate of 5%. Both notes haveEach note originally had a maturity date of August 1, 2019. During the third quarter, the Company finalized an eighteen-month extension that extended the maturity date to March 1, 2021. The promissory notes including interest, hadhave an aggregate outstanding balancesbalance of approximately $130,000 and $181,000$95,000 at September 30, 2017 and December 31, 2016, respectively.

Expected future payments related to the promissory notes as of September 30, 2017, are approximately as follows:

For the year ending:

December 31, 2017 $17,000 
December 31, 2018  68,000 
December 31, 2019  45,000 
  $130,000 

2019. The Company paidincurred interest expense related to the promissory notes for the three and nine months ended September 30, 20172019 in the amount of approximately $1,700$400 and $5,500,$2,500, respectively; no interest expense was incurred during 2018 as these notes were assumed on January 8, 2019.

The Company’s interest expense of approximately $50,000 and $121,000 for the three and nine months ended September 30, 2018, respectively, was related to convertible debt not assumed in the Merger as of January 8, 2019.

Convertible Notes

The Convertible Notes payable represents a securities purchase agreement with select accredited investors, which was assumed in the Merger. The debt assumed by the Company consisted of $750,000 of units (the “Units”) with a purchase price of $50,000 per Unit. Each Unit consists of (i) a 12% senior secured convertible note, initially convertible into shares of the Company’s common stock, par value $0.001 per share, at a conversion price equal to the lesser of $0.40 or ninety percent (90%) of the per share purchase price of any shares of common stock or common stock equivalents issued in future private placements of equity and/or debt securities completed by the Company following this offering, and (ii) a three-year warrant to purchase such number of shares of the Company’s common stock equal to one hundred percent (100%) of the number of shares of common stock issuable upon conversion of the notes at $0.40. The Warrants were initially exercisable at a price equal to the lesser of $0.75 or ninety percent (90%) of the per share purchase price of any shares of common stock or common stock equivalents issued in future private placements of the debt and/or equity securities completed by the Company following the issuance of warrants. The Convertible Notes are secured by all of the assets of the Company.

The Company recorded the proceeds from the notes and the accompanying warrants, which accrete over the period the notes are outstanding, on a relative fair value basis of $505,424 and $244,576, respectively. Interest expense related to the discount on these convertible notes for the three and nine month period ending September 30, 2019 was approximately $24,000 and $151,900, respectively. The Company paidrecognized approximately $19,300 and $60,500, respectively, in unpaid accrued interest expense related to the promissory notes for the three and nine months ended September 30, 20162019.

The Convertible Notes sold in the amountoffering were initially convertible into an aggregate of 1,875,000 shares of common stock. The down round feature was triggered on January 8, 2019, and the conversion price of the Convertible Notes was adjusted to $0.36. The Company recognized the down round as a deemed dividend of approximately $800$288,000 which reduced the income available to common stockholders.

On February 6, 2019, $100,000 of the Company’s $750,000 outstanding Convertible Notes plus accrued interest was converted into an aggregate of 251,667 shares of common stock, eliminating $100,000 of the Company’s debt obligation. The debt was converted into shares at $0.36 per share, which was the conversion price per the SPA subsequent to the trigger of the down round feature. The convertible notes had maturity dates between August and $6,100, respectively. September 2019.

The Company had unpaidnegotiated a short-term extension with two of the three noteholders through the expected closing of the Series D Security Purchase Agreement (the “Short-term Extension Notes”). As of September 30, 2019, approximately $479,000, which includes the principal balance of $350,000, fees and penalties of approximately $80,000 and accrued interest of approximately $49,000 is due to the two Short-term Extension Notes noteholders.

The Company also reached an extension with the third noteholder which extended the maturity date of the loan for one year, until September 30, 2020. This note has a principal balance of $300,000 plus penalties of approximately $85,000 and accrued interest of approximately $40,000 for a total amount due of approximately $425,000 (the “New Principal”) as of September 30, 2019. This amount has been rolled into a new note effective September 30, 2019 (the “One Year Extended Note”). Additionally, approximately 424,000 warrants were issued in connection with the One Year Extended Note. The fair market value of the warrants on September 18, 2019, the day the warrants were issued, was approximately $106,000, which the Company recognized as an expense in the amount of approximately $69,000 atthree months ended September 30, 20172019.

In the aggregate, the new principal balance on these convertible notes as of September 30, 2019 is approximately $775,000 which is comprised of the original principal balance of $350,000 on the Short-term Extension Notes plus $425,000 for the New Principal on the One Year Extended Note.

Note 12 – Derivative Liability Warrants

In connection with the securities purchase agreements executed in May 2018 the Company issued 108,250 shares of the Company’s Series B Convertible Preferred Stock (the “Series B Shares”) and December 31, 2016 relatedwarrants to purchase 2,312,500 shares of the Company’s common stock. The warrants had a three-year term at an exercise price of $0.75. The warrants contain two features such that in the event of a downward price adjustment the Company is required to reduce the strike price of the existing warrants (first feature or “down round”) and issue additional warrants to the promissory notes.award holders such that the aggregate exercise price after taking into account the adjustment, will equal the aggregate exercise price prior to such adjustment (second feature or “additional issuance”).

 

 -11-

On January 8, 2019 the Company issued equity securities which triggered the down round and additional issuance warrant features. As a result, the exercise price of the warrants was lowered from $0.75 to $0.40 and 2,023,438 additional warrants were issued. The inclusion of the additional issuance feature caused the warrants to be accounted for as liabilities in accordance with ASC Topic 815.

 

The fair market value of the warrants, approximately $1,200,000, has been recorded as a derivative liability in the purchase price allocation as a measurement period adjustment during the period ended September 30, 2019 (see Note 3). The derivative liability has been remeasured to fair value at the end of each reporting period and the cumulative change in fair value, approximately $884,000, has been recorded as a component of other income (expense) in the Company’s consolidated statement of operations for the three and nine month period ended September 30, 2019. The fair value of the derivative liability included on the consolidated balance sheet was approximately $332,000 as of September 30, 2019.

Note 10 –13 - Common Stock Warrants

 

Fair value measurement valuation techniques, to the extent possible, should maximize the use of observable inputs and minimize the use of unobservable inputs. The Company’s fair value measurements of all warrants are designated as Level 21 since all of the significant inputs are observable and quoted prices used for volatility were available for the four comparative companies in an active market.

 

A summary of the Company’s warrant issuance activity and related information for the nine months ended September 30, 20172019 is as follows:

 

  Shares  Weighted Average
Exercise
Price
  Weighted
Average
Remaining Contractual Life
 
Outstanding at 12/31/2016  3,504,847  $

2.14

   3.24 
             
Issued  3,889,368  $1.37   4.48 
Cancelled  (200,000) $1.625    
Outstanding and exercisable at 9/30/2017 $7,194,215  $1.74   3.61 
  Shares  Weighted
Average
Exercise
Price
  Weighted
Average
Remaining
Contractual
Life
 
Assumed as of the January 8, 2019 merger  12,108,743  $1.38   1.78 
             
Issued  20,647,437  $0.72   2.36 
Outstanding and exercisable at September 30, 2019  32,756,180  $.96(1)(2)  2.15 

 

As described in Note 7, 200,000 warrants were cancelled and 200,000 shares of common stock were issued to the Noteholders’ as consideration for converting the Company’s short-term debt.

 

The fair value of all warrants issued are determined by using the Black-Scholes-MertonBlack-Scholes valuation technique and were assigned based on the relative fair value of both the common stock and the warrants issued.

The inputs used in the Black-Scholes-MertonBlack-Scholes valuation technique to value each of the warrants issued at September 30, 20172019 as of their respective issue dates are as follows:

 

Event
Description
 Date  MDVX
Stock Price
  Exercise Price of Warrant  Grant Date Fair Value  Life
of Warrant
  Risk Free Rate of Return (%)  Annualized Volatility Rate (%) 
Private Placement  2/8/17  $1.04  $1.50  $0.75   5 years   1.81   104.49 
Private Placement  7/14/17  $0.91  $1.15  $0.36   5 years   1.87   51.79 
Event
Description
 Date H-CYTE
Stock Price
  Exercise Price of Warrant  Grant Date Fair Value  Life
of Warrant
 Risk Free Rate of Return (%)  Annualized Volatility Rate (%) 
Private placement 1/8/2019 $0.40  $0.75  $0.24  3 years  2.57   115.08 
Antidilution provision(3) 1/8/2019 $0.40  $0.40  $0.28  3 years  2.57   115.08 
Private placement 1/18/2019 $0.40  $0.75  $0.23  3 years  2.60   114.07 
Private placement 1/25/2019 $0.59  $0.75  $0.38  3 years  2.43   113.72 
Private placement 1/31/2019 $0.54  $0.75  $0.34  3 years  2.43   113.47 
Private placement 2/7/2019 $0.57  $0.75  $0.36  3 years  2.46   113.23 
Private placement 2/22/2019 $0.49  $0.75  $0.30  3 years  2.46   113.34 
Private placement 3/1/2019 $0.52  $0.75  $0.33  3 years  2.54   113.42 
Private placement 3/8/2019 $0.59  $0.75  $0.38  3 years  2.43   113.53 
Private placement 3/11/2019 $0.61  $0.75  $0.40  3 years  2.45   113.62 
Private placement 3/26/2019 $0.51  $0.75  $0.32  3 years  2.18   113.12 
Private placement 3/28/2019 $0.51  $0.75  $0.31  3 years  2.18   112.79 
Private placement 3/29/2019 $0.51  $0.75  $0.31  3 years  2.21   112.79 
Private placement 4/4/2019 $0.48  $0.75  $0.29  3 years  2.29   112.77 
Private placement 7/15/2019 $0.53  $1.00  $0.31  3 years  1.80   115.50 
Convertible debt extension 9/18/2019 $0.40  $0.75  $0.25  3 years  1.72   122.04 

(1)Warrants issued with the May 2018 private placement and debt conversion had an initial exercise price of $0.75 and contain a contingent feature which would adjust the exercise price of the warrant in the event the Company issues any shares of common stock or common stock equivalents in a private placement of equity or debt securities at a price less than $0.75 per share. On August 8, 2018, the Company completed the issuance of convertible debt at an initial conversion price of $0.40. Accordingly, the exercise price on these warrants was adjusted downward to $0.40.

(2)Warrants issued with the August 8, 2018 and September 28, 2018 convertible notes had an initial exercise price of $0.75 and contain a contingent feature which would adjust the exercise price of the warrants in the event the Company issued any shares of common stock or common stock equivalents in a private placement of equity or debt securities to 90% of the issuance price if it is less than $0.75.

(3)The Company had warrants that triggered the required issuance of an additional 2,023,438 warrants as a result of the Company’s capital raise that gave those new investors a $0.40 per share investment price which required the old warrant holders to receive additional warrants since their price was $0.75 per share.

 

The methods described above may produce a fair value calculation that may not be indicative of net realizable value or reflective of future fair values. Furthermore, while the Company believes its valuation methods are appropriate and consistent with other market participants, the use of different methodologies or assumptions to determine the fair value of certain financial instruments could result in a different fair value measurement at the reporting date.

Note 11 – Revenue

The Company’s first sale of the DenerveX System occurred in July 2017. The Company recorded revenue for the three and nine months ended September 30, 2017 of $117,277.

The Company sells the DenerveX System through a combination of direct sales and independent distributors in international markets. The Company recognizes revenue when title to the goods and risk of loss transfers to customers, provided there are no material remaining performance obligations required of the Company or any matters of customer acceptance. We only record revenue when collectability is reasonably assured.

Revenue recognition occurs at the time product is shipped to customers from the third-party distribution warehouse located in Berlin, Germany. Our stocking distributors, who sell the products to their customers or sub-distributors, contractually take title to the products and assume all risks of ownership at the time of shipment. Our stocking distributors are obligated to pay us the contractually agreed upon invoice price within specified terms regardless of when, if ever, they sell the products. Our direct customers do not have any contractual rights of return or exchange other than for defective product or shipping error.

 -12-

Note 12 – Discontinued operations

Effective December 7, 2016, the Company sold all Streamline related assets after the Board authorized management to seek buyers for Streamline in May 2016. The Company sought additional funds to complete the development and launch of the Company’s primary product, the DenerveX System, and the decision to sell the Streamline assets helped raise part of the necessary funds required for continuing operations of the Company in a non-dilutive manner to existing shareholders.

The results of the discontinued operations, which represents Streamline’s IV Suspension System (“ISS”), for the three and nine months ended September 30, 2017 and 2016 are as follows:

  Three Months Ended September 30,  

Nine Months Ended

September 30,

 
  2017  2016  2017  2016 
Revenues $  $  $  $ 
Operating Expenses                
General and administrative     54,606   1,163   199,237 
Research and development           59,418 
Depreciation and amortization           189,652 
Impairment loss           1,584,048 
Total Operating Expenses     54,606   1,163   2,032,355 
Operating Loss     (54,606)  (1,163)  (2,032,355)
Other Expenses                
Interest expense     2,417      7,776 
Total Other Expenses     2,417      7,776 
Net Loss $  $(57,023) $(1,163) $(2,040,131)

Cash flows from discontinued operations are as follows:

  Nine Months Ended September 30, 
  2017  2016 
Cash Flows used in Operating Activities $(1,163) $(425,011)
Cash Flows used in Investing Activities      
Cash Flows used in Financing Activities     (39,630)
Net Cash Used in Discontinued Operations $(1,163) $(464,641)

No amortization expense was recognized related to the discontinued intangible assets for the three and nine months ended September 30, 2017. Amortization expense related to the discontinued intangible assets for the three and nine months ended September 30, 2016 was approximately $0 and $190,000, respectively.

No depreciation expense was recognized for the three and nine months ended September 30, 2017. Depreciation expense amounted to $21 and $129, respectively, for the three and nine months ended September 30, 2016.

Note 13 - Income Taxes

For the period from February 1, 2013 (inception) to September 30, 2017, the Company has incurred net losses and, therefore, has no current income tax liability. The net deferred tax asset generated by these losses, which principally consist of start-up costs deferred for income tax purposes, is fully reserved as of September 30, 2017 and December 31, 2016, since it is currently more likely than not that the benefit will not be realized in future periods.

The Company is required to file federal income tax returns and state income tax returns in the states of Florida, Georgia and Minnesota. There are no uncertain tax positions at September 30, 2017 or December 31, 2016. The Company has not undergone any tax examinations since inception.

 -13-

Note 14 - Related-Party Transactions

Royalty Agreement

The Company has a Contribution and Royalty Agreement with Dr. Haufe. The agreement provides for the Company to pay Dr. Haufe royalties equal to 1% of revenues received by the Company from sales of all products derived from the use of the DenerveX technology. No royalties have been paid as of September 30, 2017. Approximately $225 is payable to Dr. Haufe as of September 30, 2017.

Co-Development Agreement

The Company entered into a Co-Development Agreement with Dr. Andrews in September 2013. The agreement provides for the Company to pay Dr. Andrews a royalty of 2% of the Company’s net sales earned from applicable product sales for at least 5 years from the effective date of the agreement. No royalties have been paid as of September 30, 2017. Approximately $446 is payable to Dr. Andrews as of September 30, 2017.

Aviation Expense

Periodically the Company may charter general aviation aircraft from TAG Aviation LLC (“TAG”), a company owned by Mr. Jarrett Gorlin. The Company believes that such aircraft charter is on terms no less favorable then it would receive from a third party. No general aviation expenses were paid to TAG for the three and nine months ended September 30, 2017. General aviation expenses paid to TAG for the three and nine months ended September 30, 2016, were approximately $9,500 and $18,500, respectively

Operating Lease

As described in Note 8, the Company pays TAG Aviation LLC, (“TAG”), a company owned by Mr. Gorlin, for month to month rental of office space at Dekalb-Peachtree Airport in Atlanta Georgia plus cost of utilities. Rent payments under this arrangement were $1,800 per month through August 31, 2016. Effective September 1, 2016, rent payments under this arrangement increased to $2,147 per month.

Rent expense and utilities cost paid to TAG Aviation amounted to approximately $9,500 and $25,000 for the three and nine months ended September 30, 2017, respectively. Rent expense and utilities cost paid to TAG Aviation amounted to approximately $7,300 and $22,000 for the three and nine months ended September 30, 2016, respectively.

Consulting Expense

As described in Note 8, the Company paid $30,000 and $85,000, respectively, for the three and nine months ended September 30, 2017 to a founding stockholder for business advisory services. The Company paid $15,000 and $40,000, respectively, for the three and nine months ended September 30, 2016.

Note 15 - Research and Development

Devicix Prototype Manufacturing Agreement

In November 2013, the Company accepted a proposal from Devicix, a Minneapolis, Minnesota based FDA registered contract designer and developer, to develop a commercially viable prototype of its product that could be used to receive regulatory approval from the FDA and other international agencies for use on humans to relieve pain associated with Facet Joint Syndrome. Through September 30, 2017, we have paid approximately $1,820,000 to Devicix, of which approximately $12,000 was included in accounts payable as of September 30, 2017.

The development work commenced in December 2013. The total estimated cost of this work at contract signing was $960,000; however, the terms of the proposal allow either the Company or the designer and developer to cancel the development work with 10-days’ notice.

The Company incurred expenses of approximately $34,000 and $273,000, respectively, for the three and nine months ended September 30, 2017. The Company incurred expenses of approximately $103,000 and $340,000, respectively, for the three and nine months ended September 30, 2016.

Denervex Generator Manufacturing Agreement

The DenerveX device requires a custom electrocautery generator for power. As described in Note 8, in November 2014, the Company contracted with Bovie to customize one of their existing electrocautery generators for use with DenerveX Device, and then manufacture that unit on a commercial basis once regulatory approval for the DenerveX is obtained. The Bovie agreement requires a base $295,000 development fee to customize the unit, plus additional amounts if further customization is necessary beyond predetermined estimates.

 -14-

The Company paid approximately $3,000 and $33,000, respectively, for the three and nine months ended September 30, 2017 to Bovie. The Company paid approximately $1,000 and $24,000, respectively, for the three and nine months ended September 30, 2016 to Bovie.

Through September 30, 2017, we have paid approximately $422,000 to Bovie related to this agreement.

Nortech Manufacturing Agreement

In November 2014, the Company selected Nortech Systems Inc. (“Nortech”), a Minneapolis, Minnesota based FDA registered contract manufacturer, to produce 315 DenerveX devices from the prototype supplied by Devicix for use in final development and clinical trials. The agreement with Nortech includes agreed upon per unit prices for delivery of the devices.

Actual work on development of the final units began in November 2014. The Company paid approximately $7,400 and $147,000, respectively, to Nortech for the three and nine months ended September 30, 2017. The Company paid approximately $250,000 and $362,000, respectively, to Nortech for the three and nine months ended September 30, 2016.

Through September 30, 2017, we have incurred expenses of approximately $891,000 to Nortech, of which approximately $41,000 was included in accounts payable as of September 30, 2017.

 

Note 16–14 - Liquidity, Going Concern and Management’s Plans

 

The Company incurred a net losslosses of approximately $4,842,000$11,616,000 and $13,185,000$2,295,000 for the nine months ended September 30, 20172019 and 2016,2018, respectively.

The Biomedical products and services division will incur losses until sufficient revenue volume and geographical coverage is attained utilizing the infusion of capital resources to expand marketing and sales initiatives.

In April 2019, the Company determined that their contract manufacturer was not able to meet the quality and quantity requirements for producing the DenerveX product. As a result, the manufacture of the DenerveX product has been temporarily suspended while the Company sources alternative manufacturing options. Additionally, in the Company’s review and evaluation of its current distribution channels, the Company has determined that many of these channels were not cost effective. As a result of the above evaluations, certain European distributor agreements were terminated, and all other representatives have been notified that the Company is temporarily suspending the manufacture and sale of the DenerveX product while the Company sources alternative manufacturing and distributor options as well as considers other product monetizing strategies, including strategic partnerships. The H-CYTE operations will continue to incur losses until the plan for the DenerveX System monetization is determined and executed.

The Company’s independent registered public accounting firm has included an explanatory paragraph with respect to our ability to continue as a going concern in its report on the Company’s consolidated financial statements for the year ended December 31, 2018. The presence of the going concern explanatory paragraph suggests that the Company may not have sufficient liquidity or minimum cash levels to operate the business. Since inception, the Company has incurred losses and anticipates that the Company will continue to incur losses until itits products can sellgenerate enough revenue to offset its operating expenses. The Company, through September 2019, raised $7,100,000 (excluding $200,000 of debt conversions) year to date.

The Company pursued raising additional funds from the sale of equity securities. On June 7, 2019 the Board of Directors approved a sufficient enough volumenew private placements securities offering up to $8,500,000 of common stock at a price of $0.50 per share, and a three-year warrant to purchase such number of shares of common stock equal to fifty percent (50%) of the DenerveX System with margins sufficient to offset expenses.  number of shares of common stock issuable as part of this offering (the “Warrants”), at an exercise price of $1.00 per share. The Company raised $100,000 from these new private placement securities since June 30, 2019. The aforementioned security offering has been terminated.

 

To date,On October 26, 2019, the Company’s primary sourceBoard of funds has been fromDirectors approved a new private placement securities offering up to $9,750,000 of Series D Preferred Stock (“Series D Preferred”). The terms of this offering are up to $9,750,000 to be raised at $.41 per share with 100% warrant coverage at $.75 per share for a term of ten years. The Series D Preferred will carry an annual 8% cumulative dividend payable upon a liquidation or redemption. For any other dividends, the issuance of debt and equity.Series D Preferred will participate with common stock on an as-converted basis.

 

As discussed in Note 7, in FebruaryOn July 25 and July 2017,26, 2019, the Company obtained approximately $2,618,000issued two promissory notes (the “Notes”) in the aggregate principal amount of $900,000 to Horne Management, LLC, and $2,469,000, respectively, netcontrolled by Mr. William E. Horne, the Chief Executive Officer of fees, in private equity financings.the Company. The Notes bear an interest rate of 5.5% per annum and are due on demand. The Company will require additional cashhas received the funds represented by the Notes. On September 26, 2019, the Company issued a promissory note to Horne Management, LLC, for $350,000. The Terms of the Note are:

12% interest rate with a maturity date of March 26, 2020.
If the Company is unable to pay the loan as of March 26, 2020, the interest rate increases to 15%.
If the Company does not pay back the principal and interest by November 26, 2019, the Company shall issue to Lender a three-year warrant to purchase 400,000 shares of the Company’s common stock at a purchase price of $0.75 per share.

The Company has certain convertible promissory notes in 2017the aggregate principal amount of approximately $650,000 that originally matured in August and September 2019. The convertible notes are secured by all of the assets of the Company. The Company negotiated an extension with two of the three noteholders through the expected closing of the Series D Preferred .There were certain fees and penalties that were negotiated along with these extensions in the aggregate amount of approximately $80,000. The Company also reached an extension with the third noteholder which extended the maturity date of the loan for one year, until September 30, 2020, plus interest and penalties. The penalties associated with the extension of this loan were approximately $125,000 as outlined in the terms of the original agreement. The total liability on these notes including principal, accrued interest, and penalties is exploring other fundraising options for 2017. No assurancesapproximately $904,000.

There can be provided regardingno assurances that the success of such efforts. Furthermore,Company will be able to obtain additional financing on commercially reasonable terms, if at all. If the Company is unable to raise sufficient financing in 2017, it could be required to undertake initiatives to conserve its capital resources, including delaying or suspending the launch of its product outside the United States and seeking FDA approval to sell its product in the United States. Delaying or suspending these initiativescurtail operations, there would raisebe substantial doubt about the Company’s ability to continue as a going concern. Cash as of September 30, 2019 was approximately $368,000. The present level of cash and the fourth quarter raise to date may not be sufficient to satisfy the Company’s current operating requirements, as such, the additional raising of funds is required.

 

The unaudited consolidated financial statements do not include any adjustments to the carrying value of amounts of its assets or liabilities that might be necessary should the Company be unable to continue as a going concern.

 

Note 1715 - Subsequent Events

 

As discussed in Note 7,Horne Management, LLC loaned H-CYTE $150,000 on October 28, 2019, for working capital purposes. The terms of the Board authorized the issuance of shares of common stock to all Board members, both current and former, in an amount equivalent to $135,000, representing their accrued but unpaid directors’ feesloan are as of September 30, 2017. In October 2017,follows:

12% interest rate with a maturity date of April 28, 2020.
If the Company does not pay back the principal and interest by December 28, 2019, the Company shall issue to Lender a three-year warrant to purchase 171,429 shares of the Company’s common stock at a purchase price of $0.75 per share.
If the Company is unable to pay the loan as of April 28, 2020, the interest rate increases to 15%.

On November 13, 2019 the Company issued a promissory note (the “Note”) with a principal amount of $235,000 to Horne Management, LLC. The Note bears an aggregateinterest rate of 115,389 shares at $1.1712% per share, which was the average closing priceannum and is due on demand. The terms of the Company’s stock this year through September 30, 2017, to fulfill this obligation. The closing price of the Company’s stock on October 30, 2017, the day the shares were issued, was $1.09 per share.note are:

 

In August 2017, the Board authorized the issuance of an aggregate of 300,000 shares of common stock to be issued to a certain member of the board of directors and a certain consultant in recognition of services performed for the Company. The common stock is to be issued as follows: 25% on the date of grant, 25% in 1 year, and the remaining 50% to be issued 2 years from the date of grant. The common stock issuance was subject to shareholder approval to increase the amount of common stock shares in the Company’s 2013 Stock Option Incentive Plan. The Company held its annual meeting of shareholders on October 18, 2017 whereby the authorization to increase the number of shares of common stock in the Plan was approved. In October 2017, the Company issued an aggregate of 75,000 shares at $1.08 per share. The closing price of the Company’s stock on October 30, 2017, the day the shares were issued, was $1.09 per share. The fair value of the common stock issued was approximately $81,750.

In August 2016, the Company received a letter from Nasdaq Markets for non-compliance with their listing rule 5550(b), which requires a minimum $2,500,000 stockholders’ equity for continued listing on the Nasdaq Capital Market (the “Minimum”). In February 2017, the Company completed a private offering which resulted in stockholders’ equity in excess of the Minimum; however, in its March 31, 2017 Form 10-Q, the Company again reported less than $2,500,000 in stockholders’ equity. In May 2017, the Company received another letter from Nasdaq notifying the Company of non-compliance and its intent to delist MedoveX stock from trading on its exchange. The Company appealed this decision. The Nasdaq Appeals Panel gave the Company until November 13, 2017, to report a shareholders’ equity number of sufficient amount to not only meet the Minimum, but large enough to ensure the Company would not go below the threshold again in the coming year based on projected expenses.

At September 30, 2017, the Company’s stockholder equity was less than the Minimum. The Company was unable to secure investment at reasonable terms and at an amount sufficient to satisfy the conditions set by the Nasdaq Appeals Panel by their deadline of November 13, 2017. On November 14, 2017, the Company received notice from Nasdaq that the Company stock would no longer trade on its exchange after November 15, 2017. The Company applied to OTC Markets to trade on its OTCQB exchange, and the Company’s stock began trading on that exchange on November 16, 2017.

  -15-12% interest rate with a maturity date of May 13, 2020.
 If the Company does not pay back the principal and interest by January 13, 2020, the Company shall issue to Lender a three-year warrant to purchase 268,571 shares of the Company’s common stock at a purchase price of $0.75 per share.
If the Company is unable to pay the loan as of April 28, 2020, the interest rate increases to 15%.

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

 

ITEM 2.MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS.

The following discussion and analysis of our financial condition and results of operations should be read in conjunction with the consolidated financial statements and the notes thereto appearing in Part I, Item 1 of this Quarterly Report. Historical results and trends that might appear in this Quarterly Report should not be interpreted as being indicative of future operations.

 

Overview

 

MedoveX was incorporated in NevadaOn July 11, 2019, Medovex Corp. (“MedoveX”) changed its named to H-CYTE, Inc. (“H-CYTE” or the “Company”) by filing a Certificate of Amendment (the “Amendment”) to the Company’s Amended and Restated Certificate of Incorporation (the “Certificate of Incorporation”) with the Secretary of the State of Nevada. The name change and the Company’s new symbol, HCYT, became effective with FINRA on July 30, 201315, 2019.

On October 18, 2018, H-CYTE (formerly named MedoveX) entered into an Asset Purchase Agreement with Regenerative Medicine Solutions, LLC, RMS Shareholder, LLC (“Shareholder”), Lung Institute LLC (“LI”), RMS Lung Institute Management LLC (“RMS LI Management”) and Cognitive Health Institute Tampa, LLC (“CHIT”), (collectively “RMS”). On January 8, 2019, the Asset Purchase Agreement was amended, and the Company acquired certain assets and assumed certain liabilities of RMS as Spinez Corp. MedoveXreported in the 8-K/A filed in March of 2019. Based on the terms of the Asset Purchase Agreement and its amendment, the former RMS members had voting control of the combined company as of the closing of the RMS acquisition. For accounting purposes, the acquisition transaction has been treated as a reverse acquisition whereby the Company is deemed to have been acquired by RMS and the historical financial statements prior to the acquisition date of January 8, 2019 now reflect the historical financial statements of RMS.

The Company’s RMS division is a healthcare medical biosciences company that develops and implements advance innovative treatment options in regenerative medicine to treat an array of debilitating medical conditions. In addition, the company is the parent companyoperator and manager of Debride, which was incorporated under the lawsvarious Lung Health Institute clinics. Committed to an individualized patient-centric approach, RMS consistently provides oversight and management of the highest quality care while producing positive outcomes. RMS offices are located in Tampa, Florida. The Lung Health Institute located in Tampa, Florida is a wholly owned subsidiary of RMS. RMS also provides oversight and management to the Lung Health Institutes located in Nashville, TN, Scottsdale AZ, Pittsburgh, PA, and Dallas, TX.

On June 21, 2019, H-CYTE entered into an agreement with Rion LLC (“Rion”) to develop a disruptive cytotherapy technology for chronic obstructive pulmonary disease (“COPD”), the fourth leading cause of death in the U.S. This agreement provides for a 10-year exclusive and extendable supply agreement with Rion to enable H-CYTE to develop proprietary biologics. This will be managed through a new Rion division of H-CYTE. Rion has established a novel technology to harness the healing power of the body. Rion’s novel exosome technology, based on October 1, 2012. science developed at Mayo Clinic, provides an off-the-shelf platform to enhance healing in soft tissue, musculoskeletal, cardiovascular and neurological organ systems.

With this agreement, Rion will serve as the product supplier and will co-develop a proprietary cellular platform with H-CYTE for the treatment of COPD. H-CYTE will control the commercial development and facilitate clinical trial investigation. After conducting joint research and development of these biologics, H-CYTE intends to pursue submission of an investigational new drug (IND) application for review ty the U.S. Food and Drug Administration (“FDA”) for treatment of COPD.

The Company is also in the business of designing and marketing proprietary medical devices for commercial use in the United States and Europe. The Company received CE marking in June 2017 for the DenerveX System, and it is now commercially available throughout the European Union and several other countries that accept CE marking. The Company’s first sale of the DenerveX System occurred in July 2017. The Company is currently seekingplans to seek approval for the DenerveX System from the FDA in the US.United States. The Company is presently reevaluating its approaches to revenue generation including the continuing use of distribution channels, source of manufacturing, and evaluating joint venture opportunities.

 

In April, the Company determined that their contract manufacturer was not able to meet the quality and quantity requirements for producing the DenerveX

The DenerveX® System consists product. As a result, the manufacture of the DenerveX Kitproduct has been temporarily suspended while the Company sources alternative manufacturing options. Additionally, in the Company’s review and evaluation of its current distribution channels, the Company has determined that many of these channels were not cost effective. As a result of the above evaluations, certain European distributor agreements were terminated, and all other representatives have been notified that the Company is temporarily suspending the manufacture and sale of the DenerveX Power Pro-40 generator. We believe that the DenerveX System can be developed in the future to encompass a number of medical applications in addition to the current application for facet joint syndrome, including pain relief.

The Company acquired the DenerveX patent on January 31, 2013 from Scott Haufe, M.D. (“Dr. Haufe”), a director ofproduct while the Company in exchange for 750,108 shares of common stock in the Companysources alternative manufacturing and a 1% royalty on all sales of anydistributor options as well as considers other product sold based on the patent.monetizing strategies, including joint venture opportunities.

 

In September 2013, we entered into a Co-Development Agreement with James Andrews, M.D. (“Dr. Andrews”), a director ofJuly 2019, the Company whereby Dr. Andrews committedsigned a new engineering feasibility proposal that will confirm a new sterilization process will be a slightly less expensive option and expand the shelf life of DenerveX from six months to further evaluatea minimum of one year and potentially up to three years. The longer shelf life will help the DenerveX Systemdistributors reach more end-users as many hospital systems and medical practitioners will not purchase medical products with less than a one-year shelf life. The Company still considers the United States to be a target market and it remains the Company’s goal to seek to make modifications and improvements to such technology. In exchange for such services, theFDA approval. The Company agreed to pay Dr. Andrews a royalty equal to two (2%) percent of the DenerveX net sales during the five (5) year term of the Co-Development Agreement. Upon the termination of the term of the Co-Development Agreement, which has a minimum term of five (5) years, the royalty payable to Dr. Andrews shall be reduced to one (1%) percent of DenerveX net sales after such termination of products covered by any U.S. patent on which Dr. Andrewsanticipates that it will do so once it is listed as a co-inventor; if any such patents are obtained. Such one (1%) percent royalty shall continue during the effectiveness of such patent. Pursuant to the Co-Development Agreement, Dr. Andrews agreed to assign any modifications or improvements to the DenerveX to the Company subject to the royalty rights described above.

We are marketing the product as a disposable, single-use kit which includes all components of the DenerveX device product. In addition to the DenerveX device itself, we have developed a dedicated Electro Surgical Generator, the DenerveX Pro-40, to power the DenerveX device.

The generator is provided to customers agreeing to purchase the DenerveX device, and cannot be used for any other purpose.

We accepted a proposal from Devicix, a Minneapolis, Minnesota third party design and development firm, in November 2013, to develop a prototype device. This proposal included a 5-phase development plan, culminating in the production ready prototype that could be used for validation purposes. We have recently completed the final stages of the build and test phase of the device, culminating in receiving CE marking to market the product in Europe. The DenerveX Kit and Pro-40 generator is now in commercial production. We anticipate very minimal, if any, additional build and test related expenses, which consists of product design verification activities, in the future as we launch the DenerveX System in Europe. Through September 30, 2017, we have paid approximately $1,820,000 to Devicix.

In November 2014, we selected Nortech Systems Inc. (“Nortech”), a Minneapolis, Minnesota based FDA registered contract manufacturer, to produce test DenerveX devices from the prototype supplied by Devicix for use in final development and non-clinical testing. The agreement with Nortech includes agreed upon per unit prices for delivery of the devices. Actual work on development of the final units began in November 2014. Through September 30, 2017, we have paid approximately $891,000 to Nortech. We are now in commercial production.

Also in November 2014, we engaged Bovie Medical Corporation (“Bovie”), a Delaware Corporation, to develop the Electro Surgical Generator and provide post production support services. Per our agreement with Bovie, we are invoiced based on deliverables produced by Bovie, which was originally supposed to amount to $295,000 upon completion of all the deliverables. Through September 30, 2017, we have paid approximately $422,000 to Bovie for production services. The original $295,000 agreement was a base number along the pathway of development. Additional requirements were incurred as the research and development process progressed and as a result certain prices increased and additional costs were incurred to further customize the DenerveX System. We are alsoback in production manufacturing on the generator.

The Company has completed the final stages of the development and verification of the DenerveX Device and the DenerveX Pro-40 power generator as a system.

 -16-

Additionally, the company has tested the DenerveX System in an extensive living tissue model under very strict Good Laboratory Practice Standards to measure, verify, and establish its effectiveness for performance as a system. Other testing will include device sterilization, shelf life verification and shipping and performance testing to very specific standards.

The DenerveX System (the DenerveX Device and the DenerveX Pro-40 generator) was successfully tested as a system by SGS, a world leader in safety performance testing, and received certification of compliance in January 2017. SGS, a highly respected testing and verification firm, tested the DenerveX System using an extensive set of testing standards.

Regulatory Approval

The Company received CE marking in June 2017 for the DenerveX System. It can now be sold throughout the European Union and countries that accept CE Mark. In the future, the Company will seek marketing clearance from the FDA for commercialization of the DenerveX System in the US.

Aside from the European Union, we may seek regulatory approval for commercialization of the DenerveX System from Columbia, Peru, Argentina, Mexico, Turkey, Israel, New Zealand, Australia and other countries. The documentation required to accompany the CE Mark to obtain regulatory approval in the aforementioned countries may include copies of the ISO 13485 certification, the SGS certificate of approval and a statement of Good Manufacturing Practices (“GMP”).

First Sales of the DenerveX System

Following receipt of the CE mark certificate in June 2017, we subsequently received the first commercial orders of the DenerveX System from multiple distributorsgenerating revenue through sales in Europe and performed the DenerveX procedure on patients clinically.

other approved countries.

Critical Accounting Policies and Estimates

 

Our discussion and analysis of our financial condition and results of operations are based on our condensed consolidated financial statements, which we have prepared in accordance with United States generally accepted accounting principles. The preparation of these condensed consolidated financial statements requires us to make estimates and assumptions that affect the reported amounts of assets and liabilities and the disclosure of contingent assets and liabilities at the date of the financial statements, as well as the reported amounts of revenues and expenses during the reporting periods. On an ongoinga continual basis, we evaluate our estimates and judgments, including those described in greater detail below.

 

We base our estimates on historical experience and on various other factors that we believe are reasonable under the circumstances, the results of which form the basis for making judgments about the carrying value of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions.

 

Our significant accounting policies are described in more detail in the notes to our consolidated financial statements for the fiscal year ended December 31, 2016,2018, included in the Company’s Annual Report on Form 10K.10-K as well as in the notes to our unaudited consolidated financial statements for the nine months ended September 30, 2019 included in this Quarterly Report on Form 10-Q. The December 31, 2018 financial information included in the Company’s Annual Report on Form 10-K reflect the historical financial information of the H-CYTE (formerly MedoveX) business and do not include the RMS financial information. With the reverse merger accounting, historical financial information for periods prior to the Merger on January 8, 2019 presented in the comparative consolidated financial statements and footnotes included in the 2019 Quarterly Reports on Form 10-Q will only reflect the historical financial information related to RMS.

 

Factors Which May Influence Future Results of Operations - Three and Nine Months Ended September 30, 2019 and 2018

 

The following is a description of factors that may influence our future results of operations, and that we believe are important to an understanding of our business and results of operations.

Revenue;Revenue, Cost of RevenueSales and Gross Profit

 

The Company’s first sale of the DenerveX System occurred in July 2017. WeCompany recorded gross revenue for the three and nine months ended September 30, 20172019 of $117,277.approximately $2,742,000 and $6,498,000, respectively. The Company recorded gross revenue for the three and nine months ended September 30, 2018 of approximately $1,537,000 and $6,881,000 respectively. The decrease in revenue for the nine months ended September 30, 2019 is mainly attributable to a decrease in the number of treatments provided by the biomedical services business (RMS). The revenue for the nine months ended September 30, 2019 is derived predominantly from RMS and the revenue for the nine months ended September 30, 2018 is exclusively RMS.

 

The Company sells the DenerveX System through a combination of direct sales and independent distributors in international markets. The Company recognizes revenue at the time product is shipped to customers from the third-party distribution warehouse in Berlin, Germany. We believe this action satisfies the performance obligation as outlined in new revenue recognition standards.

The DenerveX Device is manufactured by Nortech in Minneapolis, MN and subsequently shipped to the third-party warehouse in packages of five units per one package. Our independent distributors then order the DenerveX Devices as single units at specified prices as outlined in their distribution agreements. The international distribution agreements also specify the pricing for which the independent distributor is to sell the DenerveX Device to their end-user customers.

The Pro-40 Generator is manufactured in Bulgaria and shipped to the third-party warehouse as single units. The generators are typically provided for use to customers at no cost, however, demo units can be purchased by customers for which the Company records in revenue.

 -17-

Our independent distribution customers place initial purchase orders for minimum stocking quantities of both the DenerveX Devices and Pro-40 Generators as agreed upon per their signed international distribution agreements. Subsequent stocking orders are required to be placed initially at specified dates and quantities based upon projected end-user sales volumes. Stocking orders thereafter are required to be placed quarterly based off actual end-user sales volumes.

Cost of sales as a percentage of revenue was approximately 82% resulting in a gross profit margin of approximately 18%.

Operating Expenses

We classify our operating expenses into four categories: research and development, sales and marketing, general and administrative, and depreciation and amortization.

Research and Development Expenses

Research and development costs and expenses consist primarily of fees paid to external service providers, laboratory supplies, costs for facilities and equipment, and other costs for regulatory, patent, and research and development activities. For the three and nine months ended September 30, 2017,2019 the Company incurred approximately $70,000$550,000 and $462,000, respectively,$1,539,000, in research and development expenses.cost of sales, respectively. For the three and nine months ended September 30, 2016,2018 the Company incurred approximately $396,000$504,000 and $772,000, respectively,$1,979,000, in researchcosts of sales, respectively. The cost of sales for the three and development expenses.nine months ended September 30, 2019 is derived predominantly from RMS and the cost of sales for the three and nine months ended September 30, 2018 is exclusively from the RMS business.

 

ResearchThe Company’s cost of sales is comprised of two main components: medical supplies and developmentpersonnel costs for the biomedical services business, RMS. Medical supplies are predominantly variable costs and based on the number of treatments provided; personnel expenses are recordedalso variable as these are hourly positions. The number of treatments currently being provided can be handled adequately with the Company’s present level of personnel. The Company possesses the opportunity to increase the number of treatments performed without increasing personnel costs as it can leverage the current personnel’s availability until the Company’s treatment volume reaches critical mass. However, upon an increase in operating expenses intreatment volume beyond that capacity, the period in which they are incurred. Estimates have been used in determining the liability of certain costs where services have been performed but not yet invoiced.Company will need to hire additional personnel.

 

We monitor levelsThe increase in cost of performance under each significant contractsales for external service providers, including the extentthree months ending September 30, 2019 as compared to the prior year is attributable to more treatments being completed. The decrease in cost of patient enrollmentsales for the nine months ending September 30, 2019 as compared to the prior year is attributable to reduced costs for medical supply purchases from cost control initiatives as well as reduced variable costs associated with reduced revenue volume and other activities through communications with the service providersability to reflectperform treatments using fewer staff members.

For the actual amount expended.three and nine months ended September 30, 2019 the Company generated a gross profit totaling approximately $2,192,000 (80%) and $4,959,000 (76%), respectively. For the three and nine months ended September 30, 2018, the Company generated a gross profit totaling $1,033,000 (67%) and $4,902,000 (71%), respectively. The increase in gross margin for the three months ending September 30, 2019 as compared to the prior year is attributable to increased revenue and less than proportional cost of sales increases from cost controls for medical supply purchases and the ability to perform treatments using fewer staff members. The increase in gross margin for the nine months ended September 30, 2019, is due to reduced cost of sales from cost controls for medical supply purchases and the ability to perform treatments using fewer staff members, net of revenue decline.

26

Operating Expenses

 

Salaries and Related Costs

For the three and nine months ended September 30, 2019, the Company incurred approximately, $1,914,000 and $7,079,000 in salaries and related costs, respectively. For the three and nine months ended September 30, 2018, the Company incurred approximately $895,000 and $3,073,000, in salaries and related costs, respectively. Included in salaries and related costs for the three and nine months ended September 30, 2019 was approximately $1,690,000 in compensation expense related to the 4,225,634 shares of common stock valued at $.40 per share issued to Mr. William E. Horne on April 25, 2019. These shares were fully-vested upon the issuance of a restricted stock award, pursuant to his employment agreement with the Company, which stated that this award would be fully vested if it was not issued within fifteen days of the Merger. The restricted stock award was not issued within that time frame and was fully vested when issued. The Company recognized approximately $1,690,000 of compensation expense in the quarter ended June 30, 2019. The remaining increase in salaries and related costs is primarily attributable to the three and nine months ended September 30, 2018 reflecting only the expenses of the RMS business and 2019 reflecting the consolidated costs for RMS and H-CYTE. Excluding the stock compensation expense of approximately $1,690,000, the Company anticipates that salaries and related costs will continue at a comparable or reduced level in the future. Salary-related expenses are currently under review in order to determine cost-saving measures to assist the Company in its pursuit of becoming a leading biomedical services company and the Company may or may not reduce these expenses going forward.

Other General and Administrative Expenses

 

For the three and nine months ended September 30, 2017,2019, the Company incurred approximately, $477,000$2,026,000 and $1,394,000, respectively,$5,310,000 in personnel costs.other general and administrative costs, respectively. For the three and nine months ended September 30, 2016,2018, the Company incurred approximately $392,000$809,000 and $1,189,000, respectively,$2,483,000, in personnel costs.other general and administrative costs, respectively. The increase in personnelis attributable to the three and nine months ended September 30, 2018 reflecting only the expenses of the RMS business and 2019 reflecting the consolidated business costs is the result of having hired a Senior Vice President of Regulatoryfor RMS and Clinical affairs in November 2016 and also a Manager of Quality in December 2016.H-CYTE.

 

Professional fees were approximately $381,000Of the total other general and $1,182,000, respectively,administrative costs, for the three and nine months ended September 30, 2017. Professional2019, professional fees were approximately $309,000$523,000 and $1,102,000, respectively, for$1,379,000, respectively. For the three and nine months ended September 30, 2016.

2018, professional fees were approximately $183,000 and $318,000, respectively. Professional fees consist primarily of accounting, legal, patent and public company compliance costs as well as regulatory costs incurred to obtainmaintain CE Mark in Europe. The Company has incurred additional accounting, consulting and legal fees due to the cost of being a public company and costs related to the reverse acquisition accounting in 2019 and 2018.

 

Travel expenses were approximately $86,000 and $188,000, respectively, forThe Company anticipates that the three and nine months ended September 30, 2017. Travel expenses were approximately $50,000 and $130,000, respectively, for the three and nine months ended September 30, 2016.

We anticipate that ourother general and administrative expenses will continue at a comparable rate in the future to support clinical trials, commercialization of our product candidate and include the continued costs of operating as a public company.

 

Sales and Marketing ExpensesAdvertising

 

For the three and nine months ended September 30, 2017,2019, the Company incurredhad approximately $217,000$1,468,000 and $450,000,$4,188,000 respectively, in salesadvertising costs, as compared to $279,000 and marketing expenses. For the three and nine months ended September 30, 2016, the Company incurred approximately $107,000 and $166,000, respectively, in sales and marketing expenses. Sales and marketing expense consists primarily of fees paid to vendors for tradeshows and consultants in correlation with the launch and commercialization of the DenerveX System in Europe. We expect these expenses will continue to increase as we launch the product in new markets and expand penetration in existing markets.

Depreciation and Amortization

Depreciation and amortization expense are recorded in the period in which they are incurred. The Company recognized approximately $7,000 and $20,000, respectively, in depreciation expense$1,436,000 for the three and nine months ended September 30, 2017.2018. The Company recognized approximately $2,000 and $6,000, respectively, in depreciation expense for the three and nine months ended September 30, 2016. The purchase of a trade show booth for sales and marketing conventions in Europe at the end of 2016 is largelyincreases were attributable to increased marketing efforts to promote the increaseCompany’s healthcare medical biosciences business. We expect these expenses will continue at a comparable rate as depreciation expensewe expand penetration in 2017.existing markets.

Depreciation and Amortization

 

For the three and nine months ended September 30, 2016,2019, the Company recognized approximately $0$212,000 and $190,000,$632,000 respectively, in depreciation and amortization expense. Amortization expense is a result of amortizingOf that, the intangible assets acquired in the Streamline acquisition in March 2015. Amortization expense is included in the total loss from discontinued operationsCompany recognized approximately $184,000 and $552,000 for the three and nine months ended September 30, 2016.

 -18-

Results of Continued Operations

Three and Nine Months Ended September 30, 2017 Compared2019, respectively, in amortization expense related to the Three and Nine Months Ended September 30, 2016

Total operating expenses decreased approximately $350,000, or 20%, to approximately $1,386,000 fortechnology intangibles that arose as a result of the reverse merger by RMS of H-CYTE. For the three months ended September 30, 2017, as compared to approximately $1,736,000 for the three months ended September 30, 2016.

Total operating expenses decreased approximately $6,318,000, or 59%, to approximately $4,466,000 for theand nine months ended September 30, 2017,2018, the Company recognized approximately $28,000 and $80,000 respectively, in depreciation expense.

Departure of Directors and Certain Officers, Election of Directors, Appointment of New Board Members and Officers.

On January 8, 2019, in connection with the APA, the Board of Directors of the Company (“the Board”) appointed Michael Yurkowsky and Raymond Monteleone as comparedadditional members of the Board.

Mr. Michael Yurkowsky is to approximately $10,784,000receive $5,000 per Board meeting. Besides this arrangement, there are no arrangements or understandings between the Company and Mr. Yurkowsky and any other person or persons pursuant to which Mr. Yurkowsky was appointed as a member of the Board and there is no family relationship between Mr. Yurkowsky and any other director or executive officer of the Company or any person nominated or chosen by the Company to become a director or executive officer.

Mr. Raymond Monteleone is to receive $5,000 per Board meeting. Besides this arrangement and the consulting agreement (see Note 8), there are no arrangements or understandings between the Company and Mr. Monteleone and any other person or persons pursuant to which Mr. Monteleone was appointed as a member of the Board and there is no family relationship between Mr. Monteleone and any other director or executive officer of the Company or any person nominated or chosen by the Company to become a director or executive officer.

On February 4, 2019, the Board accepted the resignation of Mr. Charles Farrahar as the Chief Financial Officer, effective immediately. Mr. Farrahar resigned as the Chief Financial Officer for personal reasons and not as a result of any disputes or disagreements between Mr. Farrahar and the Company on any matter relating to the Company’s operations, policies, accounting policies, or practices.

On February 4, 2019, the Board of the Company appointed Mr. Jeremy Daniel as the Chief Financial Officer of the Company. There are no arrangements or understandings between the Company and Mr. Daniel.

On February 15, 2019, Dennis Moon resigned from his position as the Executive Vice President of the Company, effective immediately. Mr. Moon resigned from his position at the Company for personal reasons, not as a result of or caused by any disagreements between Mr. Moon and the Company on any matter relating to the Company’s operations, policies, or practices.

On June 7, 2019, the Board appointed Briley Cienkosz as Chief Marketing Officer, Gary Mancini as Chief Relationship Officer, and Ann Miller as Chief Operating Officer of the Company. There are no arrangements or understandings between the Company and these new officers. There are no family relationships between the new officers and any other director or executive officer of the Company, or any person nominated or chosen by the Company to become a director or executive officer.

On July 29, 2019, the Board appointed Dr. Andre Terzic to the Board. Dr. Andre Terzic, 57, has served as a director at the Center for Regenerative Medicine of Mayo Clinic in Rochester, Minnesota for the nine months ended September 30, 2016. The significant decreaselast five years. Dr. Andre Terzic is the resultChair of the goodwill impairment lossPharmaceutical Science and Clinical Pharmacology Advisory Committee of approximately $6,456,000 that was recognized in June 2016 withFood and Drug Administration, the write-downPresident of the Streamline related intangible assets. Impairment charges aside, total operating expenses would have approximated $4,329,000American Society for Clinical Pharmacology & Therapeutics, and one of the co-founders of Rion. Rion is a Minnesota Bio-tech Company focused on cutting-edge regenerative technologies. Dr. Terzic received his M.D. at University of Belgrade in Paris, France in 1985 and his Ph.D. from the Department of Pharmacology of University of Illinois in 1991.

On July 30, 2019, the Board appointed Dr. Atta Behfar as a member of the Board. Dr. Atta Behfar, 42, has worked as a cardiologist at the Department of Cardiovascular Medicine of Mayo Clinic for the nine months ended September 30, 2016, resulting in an increase of approximately $138,000, or 3%, for the nine months ended September 30, 2017.

Without the impairment charges, total operating expenses for the nine-month period ending September 30, 2017 were more comparable to the prior year for the same period. The hiring of two employees at the beginning of 2017last five years. Dr. Atta Behfar is attributable to the increase as salaries and wages expense increased. Research and development expenses decreased significantly as we completed the final stagesa Director of the developmentVan Cleve Cardiac Regenerative Medicine program at Mayo Clinic and verificationone of the DenerveX Systemfounders of Rion. Dr. Behfar received a Bachelor of Science degree in Biochemistry from Marquette University in 1998 and applied for CE Mark certification. However, the reductiona M.D. and Ph.D. from Mayo Clinic College of Medicine, Mayo Graduate School in research and development costs were similarly offset with an increase in Sales & Marketing expenses as we entered commercial production of the DenerveX System. We continued to incur similar costs associated with being a public entity.

Results of Discontinued Operations

Our discontinued operations generated net losses of approximately $1,000 and $2,040,000, respectively, for the nine months ended September 30, 2017 and 2016.2006.

 

Funding Requirements

 

We anticipate our cash expenditures will remain consistentincrease as we continue to operate as a publicly traded entity, and as we move forward with increased sales and marketing initiatives for the recent commercializationBiomedical products and services and investing in the Rion division and as we incur losses associated with temporarily suspending the manufacture and sale of the DenerveX System onto clinical trial studies. We expect future cash flow expendituresproduct. In addition, the Company is pursuing the acquisition of new technologies to increase ifexpand the FDA requires a de novo regulatory path, insteadbusiness lines and with the intent of a 510(k) approval.increasing profitability.

 

To the extent our availableThe present level of cash is insufficient to satisfy our long-termcurrent operating requirements, we will need to seekrequirements. The Company is seeking additional sources of funds from the sale of equity or debt securities or through a credit facility, or we will need to modify our current business plan.facility. There can be no assurances that we will be able to obtain additional financing on commercially reasonable terms, if at all.

 

The Company is pursuing raising additional funds from the sale of additional equity or convertible debtsecurities. On June 7, 2019 the Board approved a new private placements securities would likely result in dilutionoffering up to our current stockholders.$8,500,000 of common stock at a price of $0.50 per share, and a three-year warrant to purchase such number of shares of common stock equal to fifty percent (50%) of the number of shares of common stock issuable as part of this Agreement (the “Warrants”), at an exercise price of $1.00 per share. The Company raised $100,000 from these new private placement securities since June 30, 2019. This offering was terminated on August 30, 2019.

The Company expects to close on $6,000,000 of the Series D Preferred offering replacing the $8,500,000 offering adopted by the Board on June 7, 2019, with an offering for up to $9,750,000. Such closing is expected to be completed by the end of November 2019.

 

Going Concern

 

OurThe Company incurred net losses of approximately $11,615,000 and $2,295,000 for the nine months ended September 30, 2019 and 2018, respectively.

The RMS products and services division will incur losses until sufficient revenue volume and geographical coverage is attained utilizing the infusion of capital resources to expand marketing and sales initiatives. The H-CYTE operations will continue to incur losses until the plan for the DenerveX System commercialization is determined and executed.

The Company’s independent registered public accounting firm has included an explanatory paragraph with respect to ourthe Company’s ability to continue as a going concern in its report on ourthe Company’s consolidated financial statements for the yearsyear ended December 31, 2016 and 2015.2018. The presence of the going concern explanatory paragraph suggests that wethe Company may not have sufficient liquidity or minimum cash levels to operate the business. Since ourits inception, we havethe Company has incurred losses and anticipateanticipates that wethe Company will continue to incur losses until ourits products can generate enough revenue to offset ourits operating expenses. We receivedThe Company, through September 2019, had raised $7,100,000 (excluding $200,000 of debt conversions) year to date in additional cash to sustain the Company. Cash as of September 30, 2019 was approximately $2,618,000$368,000. The present level of net proceeds in a private placementcash is insufficient to satisfy our current operating requirements.

The Company is pursuing raising additional funds from the sale of commonequity securities. In the third quarter of 2019, the Company raised $100,000 by selling 200,000 shares of commons stock in February 2017. Weat $0.50 per share. The Company also received approximately $2,469,000issued the investors 100,000 warrants with an exercise price of net proceeds from another private placement$1.00 per share. The Company expects to close on $6,000,000 of common stock in July 2017. We believe these fundsthe Series D Preferred offering replacing the $8,500,000 offering adopted by the Board on June 7, 2019, with an offering for up to $9,750,000. Such closing is expected to be completed by the end of November 2019.

There can be no assurances that the Company will be sufficientable to maintain uninterrupted operations while we pursue our near term operational plans and pursue other fund-raising initiatives that will be required in 2017. No assurances can be provided regarding the success of such efforts. Furthermore,obtain additional financing on commercially reasonable terms, if at all. If the Company is unable to raise sufficient financing in 2017, it could be required to undertake initiatives to conserve its capital resources. If we are required to conserve resources or curtail production,operations, there couldwould be substantial doubt about the Company’s ability to continue as a going concern.

 

Liquidity and Capital Resources

 

Since ourits inception, we havethe Company has incurred losses and anticipateanticipates that we will continue to incur losses infor the foreseeable future.

 

While we expect our research and development costs for the DenerveX System to dissipate, we also anticipate increased expenditures for clinical trials to obtain FDA approval of the DenerveX System as well as expenses related to the commercial launch of the DenerveX system. We will need additional cash to fully fund these activities.

 -19-

Sources of Liquidity

 

Equity

 

On February 9, 2017,January 8, 2019, the Company entered into a Unit Purchase Agreementsecurities purchase agreement (the “SPA”) with selected accredited investors wherebyfour purchasers (the “Purchasers”) pursuant to which the four Purchasers invested in the Company hadan aggregate amount of $2,000,000, with $1,800,000 in cash and $200,000 by cancellation of debt as explained below, in exchange for forty (40) units (the “Units”), each consisting of a convertible note (the “Convertible Note”) with the rightprincipal amount of $50,000 and a warrant (the “Warrant”) to sell in a private placementpurchase common stock (the “common stock”) of the Company. Pursuant to this SPA, the Company initially offered a minimum of $3,000,000$1,000,000 and upa maximum of $6,000,000, and subsequently increased to a maximum of $5,000,000$8,000,000 (the “Maximum Amount”) of units. Each Unit hadUnits at a purchase price of $100,000 and consisted$50,000 per Unit until the earlier of (i) 96,154 sharesi) the closing of the subscription of the Maximum Amount and ii) March 31, 2019 (the “Termination Date”), subject to the Company’s common stock, par value $0.001 per shareearlier termination at a purchase price of $1.04 per share,its discretion. The SPA includes the customary representations and (ii) a warrant to purchase 48,077 shares of common stock. Each warrant has an initial exercise price of $1.50 per share and is exercisable for a period of five (5) yearswarranties from the dateCompany and purchasers. Steve Gorlin, the Company’s former Chairman of issuance.the Board, converted a $200,000 promissory note owed to him by the Company in exchange for four (4) Units on the same terms as all other Purchasers.

 

The offering resultedEach Convertible Note offered by the Company as part of the Unit bears an interest rate of 12% per annum, has a principal amount of $50,000, shall mature in gross proceeds of $3,022,000one year from the original issue date on January 8, 2019, and resulted in the issuance of an aggregate of 1,631,730 shares of common stock, 12,740 shares of Series A Preferred Stock and warrants to purchase 2,005,761 shares of common stock. The placement agent collected an aggregate of approximately $350,000 in total fees related to the offering and warrants to purchase an aggregate of 405,577will be convertible into shares of common stock at a price of $1.50 per share.

Each share$0.40 subject to adjustment stated in the Convertible Note. Pursuant to the terms of Series A Preferred Stock may be converted into sharesthe Convertible Note, each holder of fully paid and non-assessablethe Convertible Notes shall not own more than 4.99% of the number of shares of common stock outstanding immediately after giving effect to the issuance of common stock issuable upon exercise of such Convertible Note. Upon default, the penalty interest rate of the Convertible Note shall rise to 18% per annum. In addition, pursuant to the SPA, the Company offers, as part of the unit, warrants to purchase the common stock at a rateprice of one hundred shares of the Company’s common stock for every$0.75 per share of Series A Preferred Stock.(the “Exercise Price”), subject to adjustments stated therein.

 

On July 14, 2017,The holder of each Warrant may purchase the Company entered into a Securities Purchase Agreement with selected accredited investors whereby the Company sold an aggregatenumber of 2,956,043 shares of common stock equal to the number of shares of common stock issuable upon conversion of each Convertible Note while the Warrant is exercisable. The Warrants have a term of three years and 1,478,022 warrants to purchaseshall be exercised in cash or on a cashless basis as described in the Warrant. All of such notes have been converted into an aggregate of 18,000,000 shares of common stock. The Offering resulted in $2,469,000 in net proceeds to the Company. The common stock shares were sold at $0.91 per share which was the closing price of the Company’s common stock on July 13, 2017, the day prior to the agreement. Each warrant has an exercise price of $1.15 and is exercisable for a period of five years commencing six months from the date of issuance.

Debt

 

On February 9, 2017,Steve Gorlin, the Company’s $1,150,000 short-termformer Chairman of the Board, converted a $200,000 promissory note payableowed to him by the Company pursuant to the same terms of the SPA entered into by other investors to consummate the acquisition in January 8, 2019. The promissory note was converted into an aggregate of 165,865500,000 shares of common stock, eliminating the Company’s debt obligation.

Debt

On July 25 and 9,399July 26, 2019, the Company issued two promissory notes (the “Notes”) in the aggregate principal amount of $900,000 to Horne Management, LLC, and controlled by Mr. William E. Horne, the Chief Executive Officer (“CEO”) of the Company. The Notes bear an interest rate of 5.5% per annum and are due on demand. The Company has received the funds represented by the Notes. On September 26, 2019, the Company issued a promissory note to Horne Management, LLC, for $350,000. The Terms of the Note are:

12% interest rate with a maturity date of April 28, 2020.
If the Company does not pay back the principal and interest by December 28, 2019, the Company shall issue to Lender a three-year warrant to purchase 171,428 shares of the Company’s common stock at a purchase price of $0.75 per share.
If the Company is unable to pay the loan as of April 28, 2020, the interest rate increases to 15%.

On October 28, 2019 the Company issued a promissory note (the “Note”) with a principal amount of $150,000 to Horne Management, LLC and controlled by Mr. William E. Horne, the CEO of the Company. The Note bears an interest rate of 12% per annum and is due on demand. The terms of the note are:

12% interest rate with a maturity date of April 28, 2019
If the Company does not pay back the principal and interest by December 28, 2019, the Company shall issue to Lender a three-year warrant to purchase 171,429 shares of the Company’s common stock at a purchase price of $0.75 per share.
If the Company is unable to pay the loan as of April 28, 2020, the interest rate increases to 15%.

On November 13, 2019 the Company issued a promissory note (the “Note”) with a principal amount of $235,000 to Horne Management, LLC and controlled by Mr. William E. Horne, the CEO of the Company. The Note bears an interest rate of 12% per annum and is due on demand. The terms of the note are:

12% interest rate with a maturity date of May 13, 2020.
If the Company does not pay back the principal and interest by January 13, 2020, the Company shall issue to Lender a three-year warrant to purchase 268,571 shares of the Company’s common stock at a purchase price of $0.75 per share.
If the Company is unable to pay the loan as of April 28, 2020, the interest rate increases to 15%.

The $750,000 convertible notes payable assumed in the Merger, had a fair value of approximately $598,000 on the acquisition date. Subsequently, on February 6, 2019, $100,000 of the outstanding Convertible Notes was converted into an aggregate of 250,000 shares of Series A Preferred Stock,common stock, eliminating $100,000 of the Company’s debt obligation. The debt was converted into shares at $1.04$0.40 per share, which was the offeringconversion price per the securities purchase agreement. The $650,000 remaining principal balance of these convertible notes mature in August and September 2019. The convertible notes are secured by all the assets of the Company.

During the third quarter, the Company negotiated extensions of for two of these convertible notes until the closing of the Series D Preferred. The third note was extended to September 2020. The total liability covered by these notes is $775,000. The extensions required certain interest adjustments and transaction fees.

The Company has certain promissory notes with outstanding balances of approximately $95,000 at September 30, 2019. The notes had a maturity date of August 1, 2019, but the Company successfully reached an agreement on August 12, 2019 for an eighteen-month extension on the notes.

In connection with the APA, on January 8, 2019, Steve Gorlin, the Company’s stockformer Chairman of the Board, converted a $200,000 promissory note owed to him by the Company pursuant to the same terms of the security purchase agreement entered into by other investors to consummate the acquisition in the February private placement.January 8, 2019. The Series A Preferred Stock is convertiblepromissory note was converted into an aggregate of 500,000 shares of common stock, at $1.04 per share.

Each share of Series A Preferred Stock may be converted into shares of fully paid and non-assessable shares of common stock at a rate of one hundred shares ofeliminating the Company’s common stock for every share of Series A Preferred Stock.debt obligation.

 

As consideration for converting the debt, the noteholders’ agreed to receive common stock in lieu of the 200,000 warrants to purchase common stock that were issued in conjunction with the short-term loan, see Note 7 of the condensed consolidated financial statements.

As a result, the 200,000 warrants were cancelled, and the Company issued to the noteholders’ an aggregate of 200,000 shares of common stock. The closing price of the Company’s stock on February 9, 2017, the day the shares were issued, was $1.04 per share. The fair value of the common stock issued was approximately $208,000.

Working Capital Surplus (Deficit) September 30, 2017  December 31, 2016 
Current Assets $2,504,000  $1,258,000 
Current Liabilities  536,000   1,851,000 
Working Capital Surplus (Deficit) $1,968,000  $(593,000) 

 -20-

Cash Flows

Cash activity for the nine months ended September 30, 20172019 and 2016the twelve months ended December 31, 2018 is summarized as follows:

 

  Nine Months Ended September 30, 
  2017  2016 
Cash used in operating activities $(3,922,000) $(4,010,000)
Cash used in investing activities  (15,000)  (6,000)
Cash provided by financing activities  4,975,000   3,360,000 
Net increase (decrease) in cash and cash equivalents $1,038,000  $(656,000)

Working Capital Deficit

  As Of 
  September 30, 2019  December 31, 2018 
Current Assets $764,000  $150,000 
Current Liabilities  7,268,000   2,193,000 
Working Capital Deficit $6,504,000  $2,043,000 

Cash Flows

Cash activity for the nine months ended September 30, 2019 and 2018 is summarized as follows:

  Nine Months Ended September 30, 
  2019  2018 
Cash used in operating activities $(7,906,764) $(2,378,418)
Cash used in investing activities  (389,577)  (207,895)
Cash provided by financing activities  8,594,590   2,412,800 
Net increase (decrease) in cash $298,249  $(173,513)

 

As of September 30, 2017,2019, the Company had approximately $1,931,000$368,000 of cash on hand.

 

Off-Balance Sheet Arrangements

 

We do not have any off-balance sheet arrangements as defined in Regulation S-K Item 303(a)(4) during the periods presented, investments in special-purpose entities or undisclosed borrowings or debt. Additionally, we are not a party to any derivative contracts or synthetic leases.

Contractual Obligations and Commercial Commitments

 

Contractual Debt Obligations

Contractual debt obligations relate to financing arrangements for D&O and general liability insurance premiums that were financed at various points throughout 2018 and the first quarter of 2019, and two promissory notes and Convertible Notes assumed in the Merger.

These insurance financing arrangements require aggregate monthly payments of approximately $18,000, reflect interest rates ranging from 7% to 12.8% and are to be paid in full by April 2020 and had balances of approximately $114,000 September 30, 2019 and $31,000 at December 31, 2018. Interest expense related to these insurance financing arrangements was approximately $2,200 and $5,200 for the three and nine months ended September 30, 2019, respectively, and was $0 for the three and nine months ended September 30, 2018 respectively.

Payments on both promissory notes assumed are due in aggregate monthly installments of approximately $5,700 and carry an interest rate of 5%. Both notes had a maturity date of August 1, 2019 and the Company was successful in reaching an agreement resulting in the extension on the notes until March 1, 2020 with no change in the interest rate and no penalties were incurred. The promissory notes had outstanding balances of approximately $103,000 at date of the Merger and approximately $95,000 at September 30, 2019.

The Convertible Notes represent a securities purchase agreement with select accredited investors, which were assumed in the Merger. The debt consisted of $750,000 of Units at a purchase price of $50,000 per Unit. Each Unit consists of (i) a 12% senior secured convertible note, initially convertible into shares of the Company’s common stock, par value $0.001 per share, at a conversion price equal to the lesser of $0.40 or ninety percent (90%) of the per share purchase price of any shares of common stock or common stock equivalents issued in future private placements of equity and/or debt securities completed by the Company following this offering, and (ii) a three-year warrant to purchase such number of shares of the Company’s common stock equal to one hundred percent (100%) of the number of shares of common stock issuable upon conversion of the notes at $0.40. The warrants were initially exercisable at a price equal to the lesser of $0.75 or ninety percent (90%) of the per share purchase price of any shares of common stock or common stock equivalents issued in future private placements of the debt and/or equity securities completed by the Company following the issuance of warrants.

The $750,000 Convertible Notes payable assumed in the acquisition transaction with RMS had a fair value of approximately $598,000 on the acquisition date. Subsequently, on February 6, 2019, $100,000 of the outstanding Convertible Notes was converted into an aggregate of 250,000 shares of common stock, eliminating $100,000 of the Company’s debt obligation. The debt was converted into shares at $0.40 per share, which was the conversion price per the securities purchase agreement. The $650,000 remaining principal balance of these convertible notes mature in August and September 2019. The Convertible Notes are secured by all the assets of the Company. The Company successfully negotiated an extension to the maturity date; for two of the three notes ($350,000) until the initial closing of the Series D Preferred and for the third note ($300,000) until September 30, 2020.

On February 6, 2019, $100,000 of the Company’s $750,000 outstanding Convertible Notes was converted into an aggregate of 277,778 shares of common stock, eliminating $100,000 of the Company’s debt obligation. The debt was converted into shares at $0.36 per share, which was the conversion price per the securities purchase agreement subsequent to the trigger of the down round feature.

On July 25, 2019 and July 26, 2019, H-CYTE, Inc. (the “Company”) issued two promissory notes (the “Notes”) in the principal amount (the “Principal Amount”) of $900,000 to Horne Management, LLC controlled by Mr. William E. Horne, the Chief Executive Officer of the Company. The Notes bear an interest rate of 5.5% per annum and are due on demand. The Company has long term contractual obligationsreceived the funds represented by the Notes.

In addition, awaiting the funding of the capital raise to be closed in the early part of the fourth quarter, the Chief Executive Officer loaned H-CYTE $350,000 on September 26, 2019, for working capital purposes. The terms of the loan as follows:

12% interest rate with a maturity date of March 26, 2020.
If the Company is unable to pay the loan as of March 26, 2020, the interest rate increases to 15%.
If the Company does not pay back the principal and interest by November 26, 2019, the Company shall issue to Lender a three-year warrant to purchase 400,000 shares of the Company’s common stock at a purchase price of $0.75 per share.

On October 28, 2019 the Company issued a promissory note (the “Note”) with a principal amount of $150,000 to Horne Management, LLC and controlled by Mr. William E. Horne, the CEO of the Company. The Note bears an interest rate of 12% per annum and is due on demand. The terms of the note are:

12% interest rate with a maturity date of April 28, 2019
If the Company does not pay back the principal and interest by December 28, 2019, the Company shall issue to Lender a three-year warrant to purchase 171,429 shares of the Company’s common stock at a purchase price of $0.75 per share.
If the Company is unable to pay the loan as of April 28, 2020, the interest rate increases to 15%.

On November 13, 2019 the Company issued a promissory note (the “Note”) with a principal amount of $235,000 to Horne Management, LLC and controlled by Mr. William E. Horne, the CEO of the Company. The Note bears an interest rate of 12% per annum and is due on demand. The terms of the note are:

12% interest rate with a maturity date of May 13, 2020.
If the Company does not pay back the principal and interest by January 13, 2020, the Company shall issue to Lender a three-year warrant to purchase 268,571 shares of the Company’s common stock at a purchase price of $0.75 per share.
If the Company is unable to pay the loan as of April 28, 2020, the interest rate increases to 15%.

Commitments

Biotechnology Agreement

The Company entered into a 10-year exclusive and extendable supply agreement with Rion that will enhance its existing cytotherapy product line, developing a disruptive technology for chronic obstructive pulmonary disease (“COPD”), the fourth leading cause of death in the U.S. Rion has established a novel technology to harness the healing power of the body. Rion’s novel exosome technology, based on science developed at Mayo Clinic, provides an off-the-shelf platform to enhance healing in soft tissue, musculoskeletal, cardiovascular and neurological organ systems.

With this agreement, Rion will serve as the product supplier and will co-develop a proprietary cellular platform with H-CYTE for the two promissory notes issuedtreatment of COPD. H-CYTE will control the commercial development and facilitate clinical trial investigation. After conducting joint research and development of these biologics, H-CYTE intends to pursue submission of an investigational new drug (IND) application for review by the BankU.S. Food and Drug Administration (“FDA”) for treatment of North Dakota New Venture Capital Program and North Dakota Development Fund. Both Notes fromCOPD.

Sublease Agreement

The Company entered into a sub-lease agreement for the Bank of North Dakota New Venture Capital Program and North Dakota Development were assumedlease in conjunction with the consummationAlpharetta, Georgia. The period of the Streamline acquisition on March 25, 2015,lease is from July 1, 2019 to December 31, 2020 and require combined monthly principalsublessee shall pay to sublessor a minimum rent, of $2,000 per month.

Consulting Agreements

The Company has reached a new agreement with Jesse Crowne, a former Director and interest paymentsCo-Chairman of $5,661 into the third quarterBoard of the Company, to provide business development consulting services for a fee of $5,000 per month. The Company incurred expense of $10,000 and $49,999, for the three and nine months ended September 30, 2019 related to this consulting agreement. Since this agreement was assumed January 8, 2019 as part of the reverse merger transaction, there were no historical costs related to this prior to January 8, 2019.

 

The Company rents commercial office spaceentered into a consulting agreement with LilyCon Investments, LLC effective February 1, 2019 for services related to evaluation and negotiation of future acquisitions, joint ventures, and site evaluations/lease considerations. The duration of the is for a period of twelve months in Alpharetta, GA. Base annual rent is currently set at $2,849the amount of $12,500 per month with a $15,000 signing bonus which was paid in full during the quarter ending March 31, 2019. The agreement also provides LilyCon Investments with $35,000 in stock (calculated using an annual Variable Weighted Average Price from February 2019 through January 2020) to be granted on the one-year anniversary of this agreement, if the agreement has not been terminated prior to that date. Either party may terminate this agreement with or without cause upon 30 days written notice. For the three and nine months ended September 30, 2019, the lease term ends July 31, 2018.Company has expensed a total of $37,500 and $115,000 in compensation to LilyCon Investments, respectively.

 

The Company also currently reimburses itsentered into an oral consulting arrangement with St. Louis Family Office, LLC, controlled by Jimmy St. Louis, former CEO Jarrett Gorlin, forof RMS, in January 2019 in the leaseamount of executive office space at a cost of $2,147$10,000 per month which it believes is at fair market value.plus benefits reimbursement for advisory services. The Company terminated this agreement effective June 30, 2019. For the three and nine months ended September 30, 2019, the Company has expensed $0 and $71,000 in consulting fees to St. Louis Family Office, respectively.

The Company entered into a consulting agreement with Strategos Public Affairs, LLC (Strategos) on February 15, 2019 for a period of twelve months, unless otherwise terminated by giving thirty days prior written notice. Strategos will provide information to key policymakers in the legislature and executive branches of government on the benefits of the cellular therapies offered by the Lung Health Institute, advocate for legislation that supports policies beneficial to patient access and oppose any legislation that negatively impacts the Company’s ability to expand treatment opportunities, and position the Company and its related entities as the expert for information and testimony. For the three and nine months ended September 30, 2019, the Company has expensed $22,500 and $48,500, respectively.

The Company entered into a consulting agreement with Goldin Solutions for media engagement and related efforts. The agreement was effective August 4, 2019 for a minimum period of six months including both proactive public relations and crisis management services, with a $33,000 monthly fee payable each month with a first month discount of $12,000. For the three and nine months ended September 30, 2019, the Company has expensed $54,000 and $54,000, respectively.

Distribution center and logistic services agreement

 

The Company has a consulting agreement with Lifeline Industries Inc., a related party, at a monthly fee of $10,000 through February 9, 2018.

The Company has consulting agreements with three sales, marketing, and distribution consultants in Europe who provide consulting services for aggregate compensation amounting to approximately €27,500 per month. The consulting agreements, while subject to modifications, commenced at separate dates and will also terminate at separate dates through April 2019.

The Company also has employment agreements with the executive officers that commit the Company to a six month severance and benefits package if those employees separate under certain conditions, including a change in control of the Company.

The Company has anon-exclusive distribution center agreement with a logistics service provider in Berlin, Germany pursuant to which they shall manage and coordinate the DenerveX System products which the Company exportsexported to the EU through June 2019. The Company pays a fixed monthly fee of €2,900€4,500 (approximately $5,000) for all accounting, customs declarations and office support, and a variable monthly fee ranging from €1,900 to €6,900 (approximately $2,300 to $8,300), based off volume of shipments, for logistics, warehousing and customer support services.

 

Nasdaq Delisting

In August 2016,Total expenses incurred for the Company received a letter from Nasdaq Marketsdistribution center and logistics agreement were approximately $10,080 and $40,080, respectively, for non-compliance with their listing rule 5550(b), which requires a minimum $2,500,000 stockholders’ equity for continued listing on the Nasdaq Capital Market (the “Minimum”). In February 2017, the Company completed a private offering which resulted in stockholders’ equity in excessthree and nine months ended September 30, 2019. Since this agreement was assumed January 8, 2019 as part of the Minimum; however, in its March 31, 2017 Form 10-Q, the Company again reported less than $2,500,000 in stockholders’ equity. In May 2017, the Company received another letter from Nasdaq notifying the Company of non-compliance and its intentreverse merger transaction, there were no historical costs related to delist MedoveX stock from trading on its exchange.this prior to January 8, 2019. The Company appealedreported a higher expense amount related to this decision. The Nasdaq Appeals Panel gave the Company until November 13, 2017, to report a shareholders’ equity number of sufficient amount to not only meet the Minimum, but large enough to ensure the Company would not go below the threshold againagreement in the coming year based on projected expenses.

At September 30, 2017, the Company’s stockholder equitysecond quarter of 2019, but it was less than the Minimum. The Company was unable to secure investment at reasonable terms and atdeemed an amount sufficient to satisfy the conditions set by the Nasdaq Appeals Panel by their deadline of November 13, 2017. On November 14, 2017, the Company received notice from Nasdaq that the Company stock would no longer trade on its exchange after November 15, 2017. The Company applied to OTC Markets to trade on its OTCQB exchange, and the Company’s stock began trading on that exchange on November 16, 2017.immaterial amount.

 

Changes in Board of DirectorsPatent Assignment and Contribution Agreements

 

On August 16, 2017The terms of a Contribution and Royalty Agreement dated January 31, 2013 with Dr. Scott Haufe, M.D was assumed in the Merger as of January 8, 2019. This agreement provides for the Company received a resignation letterto pay Dr. Haufe royalties equal to 1% of revenues earned from Mr. Steve Gorlinsales of any and all products derived from his position as a director and Co-Chairmenthe use of the BoardDenerveX technology. Royalties are payable to Dr. Haufe within 30 days after the close of Directorseach calendar quarter based on actual cash collected from sales of applicable products. The royalty period expires on September 6, 2030.

The Company incurred approximately $0 and $1,100 respectively, in royalty expense under the Contribution and Royalty agreement for the three months and nine months ended September 30, 2019, all of which was included in accounts payable at September 30, 2019. Since this agreement was assumed January 8, 2019 as part of the Company. ThereMerger, there were no disagreements between Mr. Gorlin and the Company.historical costs related to this prior to January 8, 2019.

 

On August 16, 2017, the Company appointed Mr. Jesse Crowne to fill Mr. Gorlin’s vacancy and to serve as a director and Co-Chairman of the Company’s Board of Directors.Guarantee

 

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The Company has guaranteed payments based upon the terms found in the management services agreements to two affiliated physicians related to LI Nashville, LI Scottsdale, LI Pittsburgh, and LI Dallas. For the three and nine months ending September 30, 2019, payments totaling approximately $42,000 and $105,000 respectively were made to these affiliates.

 

ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK.

 

Not applicable to smaller reporting companies.

 

ITEM 4. CONTROLS AND PROCEDURES.

 

Evaluation of Disclosure Controls and Procedures

OurThe Company maintains “disclosure controls and procedures” as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended (the “Exchange Act”), that are designed to ensure that information required to be disclosed by us in reports we file or submit under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms, and that such information is accumulated and communicated to the Company’s management, assessedincluding its Chief Executive Officer, Chief Financial Officer, and Board of Directors, as appropriate, to allow timely decisions regarding required disclosures.

In designing and evaluating the Company’s disclosure controls and procedures, management recognizes that disclosure controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired objectives, and the Company necessarily is required to apply its judgment in evaluating the cost-benefit relationship of possible disclosure controls and procedures.

The Company’s management, including its Chief Executive Officer and Chief Financial Officer, evaluated the effectiveness of our internal control over financial reportingthe design and operation of the Company’s disclosure controls and procedures as of September 30, 2017. In making this assessment, management used2019 and concluded that the criteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission (“COSO”) inInternal Control-Integrated Framework. Based on our assessment, management concluded thatCompany has a material weakness existed in internal control over financial reportingdisclosure controls and our disclosure controls. To achieve proper segregationprocedures as of accounting related duties, the Company hired additional staff subsequent to September 30, 2017,2019.

The Company has an ineffective control environment due to whom duties havea lack of internal resources with expertise to determine entries and disclosures related to some of the Company’s more complex transactions. Management believes this lack of internal expertise has been allocated sosomewhat mitigated by continuing to retain consultants with this expertise in the quarter ended September 30, 2019. This material weakness canin the Company’s disclosure controls and procedures will be corrected.further remediated in 2019.

 

Changes in Internal Control Over Financial Reporting

During the quarternine months ended September 30, 2017,2019, there were no changes in ourthe Company’s internal control over financial reporting (as defined in Rule 13a-15(f) and 15d-15(f) under the Exchange Act) that have materially affected, or that are reasonably likely to materially affect, ourthe Company’s internal control over financial reporting.

 

PART II – OTHER INFORMATION

 

ITEM 1. LEGAL PROCEEDINGS.

 

We areThe Company is not a party to any pending legal proceeding, nor is ourthe Company’s property the subject of a pending legal proceeding. None of ourthe Company’s directors, officers or affiliates are involved in a proceeding adverse to our business or has a material interest adverse to ourthe Company’s business.

 

ITEM 1A. RISK FACTORS.

 

We are a smaller reporting company as defined by 17 CFR 229.10(f)(1). Thus, we are not required to provide information under this item.

 

ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS.PROCEEDS.

 

In conjunction withDuring the Company’s offering in July 2017,three months ended September 30, 2019, the Company received proceeds of $100,000 and issued 200,000 of common stock at a price of $0.50 per share, and a three-year warrant to purchase 100,000 shares of common stock at an aggregateexercise price of 1,478,022 warrants pursuant to the exemption set forth in Regulation D.$1.00 per share.

 

ITEM 3. DEFAULTS UPON SENIOR SECURITIES.

 

None.

 

ITEM 4. MINE SAFETY DISCLOSURES.

 

Not applicable.

 

ITEM 5. OTHER INFORMATION.

 

Not applicable.

 

ITEM 6. EXHIBITS.

The exhibits listed in the accompanying Exhibit Index are filed, furnished or incorporated by reference as part of this Quarterly Report on Form 10-Q.

 

35 -22-
 

 

SIGNATURES

 

Pursuant to the requirements 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: November 20, 201714, 2019

 

 MEDOVEX CORPH-CYTE, INC
  
 By:/s/ Jarrett GorlinWilliam E. Horne
  Jarrett GorlinWilliam E. Horne
  

Chief Executive Officer

(Principal Executive Officer)

   
 By:/s/ Charles FarraharJeremy Daniel
  Charles FarraharJeremy Daniel
  

Chief Financial Officer

(Principal Financial Officer and

Principal Accounting Officer)

 -23-

EXHIBIT INDEX

 

31.1 Section 302 Certification of Principal Executive Officer*
31.2 Section 302 Certification of Principal Financial Officer*
32.1 Section 906 Certification of Principal Executive Officer and Principal Financial Officer***
101.INS XBRL Instance Document **
101.SCH XBRL Taxonomy Extension Schema Document **
101.CAL XBRL Taxonomy Calculation Linkbase Document **
101.LAB XBRL Taxonomy Labels Linkbase Document **
101.PRE XBRL Taxonomy Presentation Linkbase Document **
101.DEF XBRL Definition Linkbase Document **

 

*Filed herewith.
  
**Pursuant to Rule 406T of Regulation S-T adopted by the SEC, these interactive data files are deemed not filed or part of a registration statement or prospectus for purposes of Section 11 or 12 of the Securities Act of 1933, are deemed not filed for purposes of Section 18 of the Securities Exchange Act of 1934, and otherwise are not subject to liability under these sections.
  
***This certification is being furnished solely to accompany this Quarterly Report pursuant to 18 U.S.C. Section 1350, and it is not being filed for purposes of Section 18 of the Securities Exchange Act of 1934 and is not to be incorporated by reference into any filing of the Company, whether made before or after the date hereof, regardless of any general incorporation language in such filing.

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