UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D. C. 20459

Washington, D.C. 20549

FORM 10-Q


(Mark One)

(Mark One)

QUARTERLY REPORT PURSUANT TO SECTIONQuarterly Report pursuant to section 13 OR 15 (d) OF THE SECURITIES EXCHANGE ACT OFor 15(d) of the Securities Exchange Act of 1934

For the quarterly period endedSeptember 30, 2014

or

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

For the transition periodQuarterly Period Ended June 30, 2015
Transition Report pursuant to section 13 or 15(d) of the Securities Exchange Act of 1934
For the Transition Period from ___________ to ____________.

Commission File No. 000-20970

COMMISSIONFILE NUMBER: 000-20970

VISION-SCIENCES,


COGENTIX MEDICAL, INC.

(Exact name of registrant as specified in its charter)

Charter)

Delaware

Minnesota, U.S.A.

13-3430173

13-3430173

(State or other jurisdiction of incorporation)

incorporation or organization)

(I.R.S. Employer
Identification Number)

40 Ramland Road South, Orangeburg, NY

10962

(Address of principal executive offices)

(Zip Code)

No.)

(845) 365-0600


5420 Feltl Road
Minnetonka, Minnesota,  55343
(Address of principal executive offices)

(952) 426-6140
(Registrant’s telephone number, including area code)


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 requirementrequirements for the past 90 days.  YesYES ☒  NoNO


Indicate by check mark whether the Registrantregistrant has submitted electronically and posted on its corporate website,Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-TS (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the Registrantregistrant was required to submit and post such files).  YesYES ☒   NoNO

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

(Check one):

Large accelerated filerAccelerated Filer ☐

Accelerated filerFiler

Non-accelerated filerNon-Accelerated Filer
(Do not check if a smaller reporting company)

Smaller reporting companyReporting Company


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

Indicate


As of August 10, 2015 the number ofregistrant had  26,186,881 shares outstanding of each of the issuer’s classes of common stock as of November 11, 2014:

Common Stock, par value of $0.01 per share

47,808,456

(Title of Class)

(Number of Shares)



outstanding.
 


VISION-SCIENCES,

Table of Contents
INDEX

COGENTIX MEDICAL, INC.

TABLE OF CONTENTS

AND SUBSIDIARIES

CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS

PartPART I.

Financial Information

FINANCIAL INFORMATION
 
 

Item 1.

Financial Statements

 
 

Condensed Consolidated Balance Sheets5
Condensed Consolidated Statements of Operations

4

7
 

Condensed Consolidated Balance Sheets

5

 Condensed Consolidated Statements of Comprehensive Loss

8

Condensed Consolidated Statement of Shareholders’ Equity9
Condensed Consolidated Statements of Cash Flows

6

10
 

Notes to the Condensed Consolidated Financial Statements

7

11
 

Item 2.

Management’s Discussion and Analysis of Financial Condition and Results of Operations

17

20
 

Item 3.

Quantitative and Qualitative Disclosures about Market Risk

25

23
 

Item 4.

Controls and Procedures

25

24
 
PART II. OTHER INFORMATION 

Part II.

Other Information

Item 1.

Legal Proceedings
24
 

Item 1.

1A.

Legal Proceedings

Risk Factors

26

24
 

Item 1A.

Risk Factors

26

Item 2.

Unregistered Sales of Equity Securities and Use of Proceeds

26

24
 

Item 3.

Defaults Uponupon Senior Securities

26

25
 

Item 4.

Mine Safety Disclosures

27

25
 

Item 5.

Other Information

27

25
 

Item 6.

Exhibits

27

25
 

Signatures

28

SIGNATURES26
Certification by the Chief Executive Officer and the Chief Financial Officer pursuant to Section 302
Certification by the Chief Executive Officer and the Chief Financial Officer pursuant to Section 906

 
As used in this report, the terms “Cogentix,””Cogentix Medical,” “Company,” “we,” “us,” “our” and similar references refer to Cogentix Medical, Inc. (formerly known as Vision-Sciences, Inc.) and our consolidated subsidiaries, and the term “common stock” refers to our common stock, par value $0.01 per share.  References to “VSCI,” “Vision-Sciences” or “Vision” generally refer to Vision-Sciences, Inc. and its consolidated subsidiaries prior to the consummation of the merger of Uroplasty, Inc. with and into Vision’s wholly-owned merger subsidiary (“Merger Sub”) on March 31, 2015 (the “Merger”), and sometimes also are used as references to our current, ongoing operations related to the historical VSCI that continue following the Merger.  References to “UPI” or “Uroplasty” generally refer to Uroplasty, Inc., and its consolidated subsidiaries prior to the consummation of the Merger, and sometimes also are used as reference to our current, ongoing operations related to the historical Uroplasty that continues following the Merger.

All share and per share amounts have been adjusted to reflect the one-for-five reverse split of Vision’s outstanding common stock effective on March 31, 2015 immediately prior to the effective time of the Merger.  All numbers and prices related to common shares and options of Uroplasty that predated the Merger have been adjusted to reflect the exchange ratio of 3.6331 shares of our common stock for each share of Uroplasty common stock, as well as the above mentioned one-for-five reverse stock split, a combined impact of 0.72662 shares of our common stock for each Uroplasty share of common stock.


CAUTIONARY NOTE REGARDING This report contains the following trademarks, trade names and service marks of ours: Vision-Sciences®, EndoSheath®, Slide-On®, EndoWipe®, The Vision System®, and Urgent® for our neuromodulation product, Macroplastique® Implants for our urological tissue bulking products, VOX® for our otolaryngology tissue bulking products, PTQ® for our colorectal tissue bulking and Uroplasty® for Uroplasty LLC, one of our subsidiaries.  This report also contains trademarks, trade names andservice marks that are owned by other persons or entities.

FORWARD-LOOKING STATEMENTS


This Quarterly Reportquarterly report on Form 10-Q contains forward-looking statements“forward-looking statements” within the meaning of Thethe Private Securities Litigation Reform Act of 1995, whichSection 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended.  Statements contained in this report that refer to our estimated or anticipated future results, including estimated synergies, or other non-historical facts are forward-looking statements that reflect our current perspective of existing trends and information as of the date of this report.  Forward-looking statements generally will be accompanied by words such as “anticipate,” “believe,” “plan,” “could,” “should,” “estimate,” “expect,” “forecast,” “outlook,” “guidance,” “intend,” “may,” “might,” “will,” “possible,” “potential,” “predict,” “project,” or other similar words, phrases or expressions.  These forward-looking statements are based on current expectations about future events affecting us and are subject to various risksuncertainties and uncertainties thatfactors relating to our operations and business environment, all of which are difficult to predict and many of which are beyond our control and could cause our actual results to differ materially from those matters expressed or implied inby our forward-looking statements.  Forward-looking statements (including oral representations) are only predictions or statements of current plans and can be affected by inaccurate assumptions we might make or by known or unknown risks and uncertainties.  By way of example and without implied limitation, such statements. Examplesrisks, uncertainties and factors that affect our business included:

·we plan to obtain additional financing, which may not be available on favorable terms at the time it is needed and which could reduce our operational and strategic flexibility;
·we may be unable to successfully integrate Uroplasty’s and Vision’s operations or realize the anticipated cost savings and other potential benefit of the merger in a timely manner, if at all. As a result, the value of our shares may be adversely affected;
·we may attempt to acquire new products or technologies, and if we are unable to successfully complete these acquisitions or to integrate acquired businesses, products, technologies or employees, we may fail to realize expected benefit or harm our existing business;
·we continue to incur losses and may never reach profitability;
·the use and acceptance of our products depends heavily upon the availability of third-party reimbursement for the procedures in which its products are used;
·we cannot predict how quickly or how broadly the market will accept our products;
·that we are subject to changing federal and state regulations that could increase the cost of doing business or impose requirements with which we cannot comply;
·the 2010 Healthcare Reform Legislation imposes an excise tax on us that we may be unable to recoup, and requires cost controls that may impact the rate of reimbursement for our products;
·changes in regulatory policy, particularly at the FDA, might adversely affect our operations;
·if we are not able to attract, retain and motivate our sales force and expand our distribution channels, our sales and revenues will suffer;
·the size and resources of our competitors may render it difficult for us to successfully compete in the marketplace;
·we are primarily dependent on sales of two product lines and our business would suffer if sales of either of these product lines decline;
·we could be subject to fines and penalties, or required to temporarily or permanently cease offering products, if we fail to comply with the extensive regulations applicable to the sale and manufacture of medical products;
·our distributors may not obtain regulatory approvals in a timely basis, or at all;
·we may not have the resources to successfully market our products, which would adversely affect our business and results of operations;
·if we cannot attract and retain our key personnel and management team, we may not be able to manage and operate successfully, and we may not be able to meet our strategic objectives;
·if third parties claim that we infringe upon their intellectual property rights, we may incur liabilities and costs and may have to redesign or discontinue selling the affected product;
·if we are unable to adequately protect our  intellectual property rights, we may not be able to compete effectively;
·product liability claims could adversely affect our business and results of operations;
·security breaches and other disruptions could compromise our information and expose us to liability, which would cause our business and reputation to suffer;
·the loss or interruption of materials from any of our key suppliers could delay the manufacture of our products, which would limit our ability to generate sales and revenues;
·if we are not able to maintain sufficient quality controls, regulatory approvals of our products by the European Union, Canada, the FDA or other relevant authorities could be delayed or denied and our sales and revenues will suffer;
·if we are not able to acquire or license other products, our business and future growth prospects could suffer;
·our business strategy relies on assumptions about the market for our products, which, if incorrect, would adversely affect our business prospects and profitability;
·we derive a significant portion of our sales and revenues from outside of the U.S. and we are subject to the risks of international operations;
·failure to comply with the U.S. Foreign Corrupt Practices Act could subject us to, among other things, penalties and legal expenses that could harm our reputation and have a material adverse effect on our business, financial condition and operating results;
·our stock is thinly traded and you may find it difficult to sell your investment in our stock at quoted prices;
·our stock price may fluctuate and be volatile;
·future sales of our common stock in the public market could lower our share price;
·our corporate documents and Minnesota law contain provisions that could discourage, delay or prevent a change in control of the company; and
·we do not intend to declare dividends on our stock in the foreseeable future.

When relying on forward-looking statements include statements about expectations about future financial results, future productsto make decisions with respect to the Company, our investors and future sales of new and existing products, future expenditures, and capital resources to meet anticipated requirements. Generally, words such as “expect,” “believe,” “anticipate,” “may,” “will,” “plan,” “intend,” “estimate,” “could,”others should carefully consider the foregoing factors and other similar expressions are intended to identify forward-looking statements. The forward-looking statements are based on our future plans, strategies, projections and predictions and involve risks and uncertainties and potential events and read our actual results may differ significantly from those discussed infilings with the forward-looking statements. Factors that might cause suchSEC, available at www.sec.gov for a difference could include, among others, the availabilitydiscussion of capital resources; the availability and adequacy of third-party reimbursement; government regulation; the availability of raw material components; our dependence on certain distributors and customers; our ability to effect expected sales; competition; technological difficulties; product recalls; general economic conditionsthese and other risks detailed in this Quarterly Report on Form 10-Q and any subsequent periodic filings we make with the Securities and Exchange Commission (“SEC”). While we believe the assumptions underlying such forward-looking statements are reasonable, there can be no assurance that future events or developments will not cause such statements to be inaccurate. All forward-looking statements contained in this report are qualified in their entirety by this cautionary note.

uncertainties.  We do not undertake anany obligation to update ouror revise any forward-looking statements to reflect future events or circumstances,statement, except as may be required by law.

  We qualify all forward-looking statements by these cautionary statements.
 
PART II. FINANCIAL INFORMATION



Item 1.Financial Statements

Vision-Sciences, Inc. and Subsidiaries

Condensed Consolidated Statements of Operations

(in thousands, except per share amounts)

ITEM 1. FINANCIAL STATEMENTS

COGENTIX MEDICAL, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited)

  

Three Months Ended

  

Six Months Ended

 
  

September 30,

  

September 30,

 
  

2014

  

2013

  

2014

  

2013

 
                 

Net sales

 $4,110  $3,968  $7,862  $7,620 

Cost of sales

  2,852   2,773   5,455   5,345 

Gross profit

  1,258   1,195   2,407   2,275 
                 

Selling, general, and administrative expenses

  2,358   2,050   4,849   5,100 

Research and development expenses

  341   428   877   847 

Operating loss

  (1,441)  (1,283)  (3,319)  (3,672)
                 

Interest expense

  (106)  (44)  (189)  (85)

Other, net

  4   7   (12)  3 

Loss before provision for income taxes

  (1,543)  (1,320)  (3,520)  (3,754)

Income tax provision

  -   3   -   3 

Net loss

 $(1,543) $(1,323) $(3,520) $(3,757)
                 

Net loss per common share - basic and diluted

 $(0.03) $(0.03) $(0.08) $(0.08)
                 

Weighted average shares used in computingnet loss per common share - basic and diluted

  46,327   46,144   46,294   46,127 


  June 30, 2015  March 31, 2015 
     
Assets    
     
Current assets:    
Cash and cash equivalents $5,996,245  $9,261,903 
Accounts receivable, net  6,450,016   7,306,653 
Inventories  4,868,685   4,825,984 
Other  902,323   749,466 
Total current assets  18,217,269   22,144,006 
         
Property, plant, and equipment, net  1,969,809   1,813,343 
Goodwill  18,749,888   18,749,888 
Other intangible assets, net  13,114,391   13,748,582 
Deferred tax assets and other  303,315   296,860 
         
Total assets $52,354,672  $56,752,679 

See accompanying notes to condensed consolidated financial statements

the Condensed Consolidated Financial Statements.
 
COGENTIX MEDICAL, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED BALANCE SHEETS

Vision-Sciences, Inc. and Subsidiaries

Condensed Consolidated Balance Sheets

(in thousands)

  

September 30,

  

March 31,

 
  

2014

  

2014

 
  

(unaudited)

     
ASSETS        

Current assets:

        

Cash and cash equivalents

 $1,395  $1,237 

Accounts receivable, less allowances of $133 and $117, respectively

  2,920   3,818 

Inventories, net

  4,221   4,194 

Prepaid expenses and other current assets

  460   455 

Total current assets

  8,996   9,704 
         

Machinery and equipment

  3,447   3,456 

Demo equipment

  1,469   1,311 

Furniture and fixtures

  247   225 

Leasehold improvements

  372   372 

Property and equipment, at cost

  5,535   5,364 

Less—accumulated depreciation and amortization

  4,549   4,302 

Total property and equipment, net

  986   1,062 

Other assets, net

  67   67 

Total assets

 $10,049  $10,833 
         

LIABILITIES AND STOCKHOLDERS' DEFICIT

        

Current liabilities:

        

Accounts payable

 $1,405  $1,217 

Accrued expenses

  880   918 

Accrued compensation

  514   474 

Deferred revenue

  310   210 

Capital lease obligations

  -   22 

Total current liabilities

  3,109   2,841 
         

Convertible debt—related party, net of discount

  24,480   22,414 

Deferred revenue, net of current portion

  128   93 

Total liabilities

  27,717   25,348 
         

Commitments and Contingencies

        

Stockholders’ deficit:

        

Preferred stock, $0.01 par valueAuthorized—5,000 shares; issued and outstanding - none

  -   - 

Common stock, $0.01 par valueAuthorized—100,000 shares;issued and outstanding—47,793 shares and 47,614 shares, respectively

  478   476 

Additional paid-in capital

  103,000   102,629 

Treasury stock at cost, 65 shares and 59 shares of common stock, respectively

  (85)  (78)

Accumulated deficit

  (121,061)  (117,542)

Total stockholders’ deficit

  (17,668)  (14,515)

Total liabilities and stockholders’ deficit

 $10,049  $10,833 

(Unaudited)

  June 30, 2015  March 31, 2015 
     
Liabilities and Shareholders’ Equity    
     
Current liabilities:    
Accounts payable $3,875,197  $3,967,975 
Interest payable  599,954   523,743 
Income taxes payable  25,602   25,998 
Accrued liabilities:        
Compensation  2,868,815   3,285,952 
Other  1,505,110   2,450,058 
Total current liabilities  8,874,678   10,253,726 
         
Convertible debt – related party, net  22,795,464   22,529,497 
Accrued pension liability  1,020,389   955,780 
Other  228,468   265,766 
         
Total liabilities  32,918,999   34,004,769 
         
Commitments and contingencies  -   - 
         
Shareholders’ equity:        
Preferred stock, $0.01 par value 5,000,000 Shares authorized; none issued or outstanding  -   - 
Common stock $.01 par value; 100,000,000 shares authorized, 26,053,081 and 25,676,212 shares issued and outstanding at June 30, 2015 and March 31, 2015, respectively
  260,532   256,763 
Additional paid-in capital  75,747,690   75,530,641 
Accumulated deficit  (55,451,989)  (51,883,229)
Accumulated other comprehensive  loss  (1,120,560)  (1,156,265)
         
Total shareholders’ equity  19,435,673   22,747,910 
         
Total liabilities and shareholders’ equity $52,354,672  $56,752,679 

See accompanying notes to condensed consolidated financial statements

the Condensed Consolidated Financial Statements.
 
COGENTIX MEDICAL, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

Vision-Sciences, Inc. and Subsidiaries

Condensed Consolidated Statements of Cash Flows

(in thousands)

(Unaudited)

  

Six Months Ended

 
  

September 30,

 
  

2014

  

2013

 

Cash flows from operating activities:

        

Net loss

 $(3,520) $(3,757)

Adjustments to reconcile net loss to net cash used in operating activities:

        

Depreciation and amortization

  318   362 

Stock-based compensation expense

  349   328 

Provision for bad debt expenses

  11   7 

Amortization of debt discount

  66   - 

Loss (gain) on disposal of fixed assets

  9   (5)

Changes in assets and liabilities:

        

Accounts receivable

  887   802 

Inventories

  (261)  (712)

Prepaid expenses and other current assets

  (5)  (117)

Accounts payable

  188   (112)

Accrued expenses

  (38)  50 

Accrued compensation

  40   (96)

Deferred revenue

  135   22 

Net cash used in operating activities

  (1,821)  (3,228)

Cash flows from investing activities:

        

Purchases of property and equipment

  (17)  (46)

Proceeds from disposal of fixed assets

  -   3 

Net cash used in investing activities

  (17)  (43)

Cash flows from financing activities:

        

Proceeds from issuance of convertible debt—related party

  2,000   3,000 

Proceeds from exercise of stock options

  25   - 

Common stock repurchased

  (7)  (28)

Payments of capital leases

  (22)  (34)

Net cash provided by financing activities

  1,996   2,938 

Net increase (decrease) in cash and cash equivalents

  158   (333)

Cash and cash equivalents at beginning of period

 $1,237  $788 

Cash and cash equivalents at end of period

 $1,395  $455 
         

Supplemental disclosure of cash flow information:

        

Cash paid during the period for:

        

Interest

 $1  $4 

Income taxes

 $-  $3 
         

Non-cash financing activities:

        

Net transfers of inventory to fixed assets for use as demonstration equipment

 $234  $187 


  
Three Months Ended
June 30,
 
  2015  2014 
     
Net sales $11,150,212  $6,384,629 
Cost of goods sold  3,652,510   791,311 
         
Gross profit  7,497,702   5,593,318 
         
Operating expenses        
General and administrative  1,893,272   1,577,368 
Research and development  1,062,460   909,444 
Selling and marketing  6,651,379   5,272,621 
Amortization  634,191   8,326 
Transaction costs  468,607   - 
   10,709,909   7,767,759 
         
Operating loss  (3,212,207)  (2,174,441)
         
Other income (expense)        
Interest income  1,582   3,012 
Interest expense  (343,555)  - 
Foreign currency exchange gain  2,998   911 
   (338,975)  3,923 
         
Loss before income taxes  (3,551,182)  (2,170,518)
         
Income tax expense  17,578   19,814 
         
Net loss $(3,568,760) $(2,190,332)
         
Basic and diluted net loss per common share $(0.14) $(0.14)
         
Weighted average common shares outstanding:        
Basic and diluted  26,053,081   15,749,869 

See accompanying notes to condensed consolidated financial statements

the Condensed Consolidated Financial Statements.
 
COGENTIX MEDICAL, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS

Vision-Sciences, Inc. and Subsidiaries

Notes

(Unaudited)

  
Three Months Ended
June 30
 
  2015  2014 
     
Net loss $(3,568,760) $(2,190,332)
Other comprehensive income (loss), net of tax:        
Foreign currency translation adjustments  57,458   (789)
Unrealized gain (loss) on available-for-sale investments  -   (743)
Pension adjustments  (21,753)  (396)
Total other comprehensive income (loss), net of tax  35,705   (1,928)
Comprehensive loss $(3,533,055) $(2,192,260)

See accompanying notes to the Condensed Consolidated Financial Statements.
COGENTIX MEDICAL, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENT OF SHAREHOLDERS’ EQUITY

Three Months Ended June 30, 2015
(Unaudited)

  Common Stock  Additional Paid-in  Accumulated  Accumulated Other Comprehensive  Total Shareholders' 
  Shares  Amount  Capital  Deficit  Loss  Equity 
             
Balance at March 31, 2015  25,676,212  $256,763  $75,530,641  $(51,883,229) $(1,156,265) $22,747,910 
                         
Share-based compensation  379,499   3,795   221,403   -   -   225,198 
                         
Exercise of stock options, net of shares exchanged  (2,630)  (26)  (4,354)  -   -   (4,380)
                         
Comprehensive loss  -   -   -   (3,568,760)  35,705   (3,533,055)
                         
Balance at June 30, 2015  26,053,081  $260,532  $75,747,690  $(55,451,989) $(1,120,560) $19,435,673 

See accompanying notes to the Condensed Consolidated Financial Statements.
COGENTIX MEDICAL, INC. AND SUBSIDIARIES

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited)

  
Three Months Ended
June 30
 
  2015  2014 
Cash flows from operating activities:    
Net loss $(3,568,760) $(2,190,332)
Adjustments to reconcile net loss to net cash used in operating activities:        
Depreciation and amortization  853,165   72,584 
Loss loss on disposal of equipment  216   1,249 
Amortization of premium on marketable securities  -   343 
Share-based compensation expense  225,198   323,304 
Amortization of discount on related party debt  265,967   - 
Long term incentive plan  (29,176)  - 
Tax expense (benefit)  (1,414)  2,205 
Deferred rent  (2,669)  22,744 
Changes in operating assets and liabilities:        
Accounts receivable, net  816,135   263,078 
Inventories  (43,959)  (92,649)
Other current assets  (50,717)  (30,323)
Interest payable  76,211   - 
Accounts payable  (90,040)  49,797 
Accrued compensation  (421,327)  94,249 
Accrued liabilities, other  (1,035,323)  (65,795)
Accrued pension liability, net  39,745   44,081 
Deferred revenue  72,080   - 
Net cash used in operating activities  (2,894,668)  (1,505,465)
         
Cash flows from investing activities:        
Proceeds from maturity of available-for-sale investments  -   3,050,000 
Purchases of property, plant and equipment  (395,387)  (52,739)
Net cash provided by investing activities  (395,387)  2,997,261 
         
Cash flows from financing activities:        
Proceeds from exercise of stock options  -   48,600 
Net cash provided by financing activities  -   48,600 
         
Effect of exchange rate changes on cash and cash equivalents  24,397   (315)
         
Net increase (decrease) in cash and cash equivalents  (3,265,658)  1,540,081 
         
Cash and cash equivalents at beginning of period  9,261,903   8,681,609 
         
Cash and cash equivalents at end of period $5,996,245  $10,221,690 
         
Cash paid during the period for income taxes $17,578  $38,700 
Cash paid during the period for interest $1,400   - 

See accompanying notes to the Condensed Consolidated Financial Statements.

(Unaudited, in thousands except number

COGENTIX MEDICAL, INC. AND SUBSIDIARIES
NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
(Unaudited)

Note 1. Summary of Significant Accounting Policies


Basis of Presentation

Cogentix Medical, Inc., headquartered in Minnetonka, Minnesota, with additional operations in New York, Massachusetts, The Netherlands and the United Kingdom, is a global medical device company. We design, develop, manufacture and market innovative proprietary technologies serving the urology, urogynecology/gyn, ENT (ear, nose and throat) and gastrointestinal markets. The Urgent® PC Neuromodulation System is an FDA-cleared device that delivers percutaneous tibial nerve stimulation (PTNS) for the office-based treatment of overactive bladder (OAB). The FDA-cleared EndoSheath® Systems combine state-of-the-art endoscopic technology with a sterile, disposable microbial barrier, providing practitioners and healthcare facilities with a solution to meet the growing need for safe, efficient and cost-effective flexible endoscopy. In the U.S. and worldwide, the Company also offers Macroplastique®, a urethral bulking agent for the treatment of stress urinary incontinence. Outside the U.S., the Company markets additional bulking agents: PTQ® for the treatment of fecal incontinence and VOX® for vocal cord augmentation.

The Company is the result of the Merger effective as of March 31, 2015 (the “effective date”) of two medical device companies, Uroplasty, Inc. and Vision-Sciences, Inc. On the effective date of the Merger, the two companies completed an all-stock merger, pursuant to which UPI merged with and into Merger Sub.  Merger Sub was the surviving company from the Merger, and changed its name to Uroplasty, LLC.   After the merger, VSCI and its consolidated subsidiaries, including Uroplasty LLC, and its subsidiaries, (the “Company,” or “our”, “us” or “we”) designs, develops, manufactures,operate under the name Cogentix Medical, Inc.

Upon closing of the Merger, the former UPI stockholders owned approximately 62.5% and markets productsthe VSCI shareholders retained approximately 37.5% of the company. Accordingly, while VSCI was the legal acquirer and issued its shares in the Merger, UPI is the acquiring company in the Merger for endoscopy –accounting purposes and the scienceMerger has been accounted for as a reverse acquisition under the acquisition method of using an instrument, known as an endoscope, to provide minimally invasive access to areas not readily visibleaccounting for business combinations. As a result, the financial statements of the Company prior to the human eye. Our products are sold throughout the world through direct sales representatives in the United States (“U.S.”) and independent distributors for the resteffective date of the world. WeMerger are the exclusive supplierhistorical financial statements of ureteroscopes toUPI, whereas the Endoscopy Divisionfinancial statements of Stryker Corporation (“Stryker”). Our largest geographic markets are the U.S.Company after the effective date of the Merger reflect the results of the operations of UPI and Europe.

We are incorporatedVSCI on a combined basis. See additional disclosure provided in Delaware, and are the successor to operations begun in 1987. In December 1990, Machida Incorporated (“Machida”) became our wholly-owned subsidiary. We own the registered trademarks Vision Sciences®, EndoSheath®, EndoWipe®, Slide-On® and The Vision System®. Not all products referenced in this report are approved or cleared for sale, distribution, or use.

Basis of Presentation and Preparation

note 2.

We have prepared the condensed consolidated financial statementsour Condensed Consolidated Financial Statements included herein according to generally accepted accounting principles in the United States of America (“U.S. GAAP”),this Quarterly Report on Form 10-Q, without audit, pursuant to the rules and regulations of the Securities and Exchange Commission (“SEC”) and include, in the opinion of management, all adjustments (normal and recurring) that we consider necessary for a fair presentation of such information. We have condensed or omitted certainCommission.  Certain information and footnote disclosures normally included in the consolidated financial statements prepared in accordance with accounting principles generally accepted in the United States of America, or GAAP, have been condensed or omitted, pursuant to thosesuch rules and regulations. Weregulations, although we believe however, that our disclosures are adequate to make the information presented not misleading.

The consolidated results of operations for theany interim periods presentedperiod are not necessarily indicative of results to be expected for thea full fiscal year.  PleaseThese Condensed Consolidated Financial Statements, presented herein, should be read these condensed consolidated financial statements in conjunction with the audited consolidated financial statements and the related notes included in our Annual Reportannual report on Form 10-K for the fiscal year ended March 31, 2015.


The Condensed Consolidated Financial Statements presented herein as of June 30, 2015 and for the three month periods ended June 30, 2015 and 2014, reflect, in the opinion of management, all material adjustments, consisting only of normal recurring adjustments, necessary for a fair presentation of the consolidated financial condition, results of operations and cash flows for the interim periods.

We have identified certain accounting policies that we consider particularly important for the portrayal of our results of operations and financial condition and which may require the application of a higher level of judgment by our management, and as a result are subject to an inherent level of uncertainty.  These are characterized as “critical accounting policies” and address revenue recognition, accounts receivable, valuation of inventory, foreign currency translation/transactions, purchase price allocation on acquisition, the determination of recoverability of long-lived and intangible assets, long-term incentive plans, share-based compensation, defined benefit pension plans and income taxes, each of which is described in our annual report on Form 10-K for the fiscal year ended March 31, 2014.

2015.  Based upon our review, we have determined that these policies remain our most critical accounting policies for the three months ended June 30, 2015 and we have made no changes to these policies during fiscal 2016.

Liquidity and Capital Resources


We have incurred substantial operating losses since our inception and there can be no assurance that we will ever achieve or sustain a profitable level of operations in the future.inception. We anticipate that we will continue to incur negative cash flows from operations during the remainder of fiscal 2015,2016, driven by continued investment in a direct sales force for the U.S. market, spending for marketing revitalizing aand for research and development, pipeline,integration of UPI and VSCI, and general business operations. As of SeptemberJune 30, 2014,2015, we had cash and cash equivalents totaling approximately $1.4$6.0 million. On June 16, 2014, we issued a convertible promissory noteWe plan to Lewis C. Pell, our Chairman, or the 2014 Note, that allowed us to borrow up to $5.0 million up to June 15, 2019. The 2014 Note was issued in accordance with a letter agreement dated May 29, 2014 with Mr. Pell, or the Prior Letter Agreement, that provided for up to $5.0 million of capital to be made available to us from Mr. Pell, subject to certain conditions and an expiration date of July 1, 2015. The Prior Letter Agreement was then terminated. As of September 30, 2014, we had $2.0 million in principal outstanding under the 2014 Note. On October 24, 2014 anobtain additional $1.0 million was drawn on the 2014 Note. Pursuant to a letter agreement dated October 28, 2014 with Mr. Pell, or the Existing Letter Agreement, Mr. Pell has agreed to provide financial assistance to us in the amount of up to $2.5 million, if necessary to support our operations, for a period ending on the earlier of (i) January 1, 2016 or (ii) our raising debt and/or equity capital in the amount of $2.5 million or more. This financial assistance, if drawn by us, would be in the form of an additional loan, share purchase, or financing transaction, on such terms as we and Mr. Pell may determine. We have not utilized the Existing Letter Agreement. We expect that our cash at September 30, 2014, together with $3.0 million remaining to be drawn under the 2014 Note at September 30, 2014, plus the $2.5 million of capital to be made available to us under the Existing Letter Agreement, subject to certain conditions and an expiration date of January 1, 2016, should be sufficient to fund our operations through at least December 31, 2015. However, if our performance expectations fall short (including our failure to generate expected levels of sales) or our expenses exceed expectations, or if the commitment under the 2014 Note or the Existing Letter Agreement become unavailable, we will need to secure additional financing and/or reduce our expenses to continue our operations. Our failure to do so would have a material adverse impact on our prospects and financial condition.during fiscal 2016.   There can be no assurance that any contemplated additional financing will be available on terms acceptable to us, if at all. If required, we believe we would be able to reduce our expenses to a sufficient level to continue to operate as a going concern.


Note 2. Business Combination - Merger Between Uroplasty, Inc. and Vision-Sciences, Inc.

The Merger has been accounted for as an acquisition of VSCI by UPI, in accordance with Accounting Standards Codification (ASC) Topic 805, "Business Combinations," using the acquisition method of accounting with UPI as the accounting acquirer. Since the Company (formerly known as Vision-Sciences), as the parent company of UPI after the Merger, is the legal acquirer, the Merger has been accounted for as a reverse acquisition.  Under these accounting standards, UPI’s total purchase price of $16.5 million is calculated as if UPI had issued its shares to VSCI stockholders and converted options and warrants to purchase VSCI shares to options and warrants to purchase UPI’s common stock.

Under the acquisition method of accounting, the total purchase price was allocated to the net tangible and intangible assets of VSCI acquired in the merger, based on their fair values at the effective date of the Merger. The estimated fair values are preliminary and based on the information that was available as of the effective date of the Merger. The Company believes that the information provides a reasonable basis for estimating the fair values, but the Company is waiting for additional information necessary to finalize these amounts, particularly with respect to the estimated fair value of intangible assets and property, plant and equipment and deferred taxes related thereto. Thus the preliminary measurements of fair value reflected are subject to changes and such changes could be significant. The Company expects to finalize the valuation and complete the purchase price allocation as soon as practicable, but no later than one year from the merger date. There were no changes during the three months ended June 30, 2015 to the preliminary measurements of fair value. The preliminary allocation of the purchase price to assets acquired and liabilities assumed is as follows:

Cash and cash equivalents $2,020,000 
Accounts receivable  4,249,000 
Inventories  4,462,000 
Other current assets  369,000 
Property, plant and equipment  817,000 
Goodwill  18,750,000 
Other intangibles  13,660,000 
Other non-current assets  97,000 
Total assets acquired  44,424,000 
     
Accounts payable and other liabilities  5,209,000 
Deferred revenue  176,000 
Convertible debt – related party  22,530,000 
Other non-current liabilities  40,000 
Total liabilities assumed  27,955,000 
     
Total purchase price $16,469,000 
 
The allocation of the purchase price to the net assets acquired and liabilities assumed resulted in the recognition of the following intangible assets:
  Amount  
Weighted Average
Life-Years
 
Developed technology $6,200,000   7 
Customer relationships  7,270,000   5 
Trade names  190,000   10 
  $13,660,000     

Summary

The supplemental unaudited pro forma net sales and net loss of Significant Accounting Policies

Ourthe combined entity had the acquisition been completed on April 1, 2013:


  
Three months ended
June 30,
2014
 
   
Supplemental pro forma combined results of operations:  
Net sales $10,137,000 
Net loss $(5,040,439)
Loss per share – basic and diluted $(0.20)

Adjustments to the supplemental pro forma combined results of operations are as follows:

 
Three months ended
June 30,
2014
 
   
Increase in amortization of intangibles $594,000 
Interest amortization on related party debt  
279,000
 
Increase in net loss $873,000 

These unaudited pro forma condensed consolidated financial statements areresults have been prepared in accordance with the rulesfor illustrative purposes only and regulations of the SEC for interim reporting and U.S. GAAP. These accounting principles require usdo not purport to make certain estimates, judgments and assumptions. We believe that the estimates, judgments and assumptions upon which we rely are reasonable, based upon information available to us at the time that these estimates, judgments and assumptions are made. These estimates, judgments and assumptions can affect the reported amounts of assets and liabilities as of the date of the financial statements as well as the reported amounts of revenues and expenses during the periods presented. To the extent there are any differences (other than nominal differences) between these estimates, judgments or assumptions and actual results, our financial statements will be affected.

In the opinion of our Company’s management, the accompanying unaudited condensed financial statements contain all adjustments (consisting of normal recurring adjustments) necessary to present fairly, in all material respects, our financial position as of September 30, 2014 and the results of operations and cash flows for the three months and six months then ended. The results of operations and cash flows for the period ended September 30, 2014 are not necessarily indicative of the results of operations that actually would have resulted had the acquisition occurred on the April 1, 2013, or cash flows to be expected for any subsequent quarter or the full fiscal year ending March 31, 2015. As of September 30, 2014, there have been no material changes to anyfuture results of the significant accounting policies described in our Report on Form 10-K for the year ended March 31, 2014.

consolidated entities.  The accompanyingunaudited pro forma condensed consolidated financial statementsinformation does not reflect any operating efficiencies and cost savings that may be realized from the accountsintegration of the Company. All significant inter-company accountsacquisition.


Note 3. Goodwill and transactionsOther Intangible Assets

Goodwill

As described in note 2, on March 31, 2015, for accounting purposes, UPI was deemed to have been eliminatedacquired VSCI for a purchase price of $16.5 million, and as a result, the Company recognized $18.7 million in consolidation.

goodwill. There was no change in the goodwill balance as of June 30, 2015.


Other Intangible Assets

Other intangible assets consisted of the following at June 30, 2015 and March 31 2015:

  June 30, 2015  March 31, 2015 
  
Gross
Carrying
Amount
  Accumulated Amortization  
Gross
Carrying
Amount
  
Accumulated
Amortization
 
Developed technology $6,200,000  $222,000  $6,200,000  $- 
Patents  5,653,000   5,572,000   5,653,000   5,564,000 
Trademarks and trade names  190,000   22,000   190,000   - 
Customer relationships  7,270,000   383,000   7,270,000   - 
  $19,313,000  $6,199,000  $19,313,000  $5,564,000 
Accumulated amortization  6,199,000       5,564,000     
                 
Net book value of amortizable intangible assets $13,114,000      $13,749,000     
For the three months ended June 30, 2015 and 2014, amortization of intangible assets charged to operations was approximately $634,000 and $8,000, respectively.  The weighted average remaining amortization period for intangible assets as of June 30, 2015 was approximately 5.75 years.

Note 4

New. Newly Adopted Accounting PronouncementsPronouncements


In May 2014, July 2015, the Financial Accounting Standards Board (FASB) has issued new accountingAccounting Standards Update (ASU) No. 2015-11, “Simplifying the Measurement of Inventory (Topic 330).”  Under the current guidance namely (“ASU”) No. 2014-09, Revenue from Contracts(i.e., ASC 330-10-352 before the ASU), an entity subsequently measures inventory at the lower of cost or market, with Customers, on revenue recognition.market defined as replacement cost, net realizable value (NRV), or NRV less a normal profit margin. An entity uses current replacement cost provided that it is not above NRV (i.e., the ceiling) or below NRV less an “approximately normal profit margin” (i.e., the floor).  The new standard provides for a five-step modelguidance requires entities to be appliedmeasure most inventory “at the lower of cost and net realizable value,” thereby simplifying the current guidance under which an entity must measure inventory at the lower of cost or market (market in this context is defined as one of three different measures). The ASU will not apply to all revenue contracts with customers as well as requires additional financial statement disclosuresinventories that will enable users to understandare measured by using either the nature, amount, timing and uncertainty of revenue and cash flows relating to customer contracts. Companies have an option to use either a retrospective approachlast-in, first-out (LIFO) method or cumulative effect adjustment approach to implement the standard. There is no option for early adoption. For public entities, thisretail inventory method (RIM).  The amendments in ASU isNo. 2015-11 are effective for fiscal years and interim periods within those years beginning after December 15, 2016. 2016, including interim periods within those fiscal years.  We do not believe the adoption of this update will have a material impact on our financial statements.

In May 2014, the FASB has issued ASU No. 2014-09, “Revenue from Contracts with Customers (Topic 606).”  The guidance in this update supersedes the revenue recognition requirements in Topic 605, “Revenue Recognition.”  In addition, the existing requirements for the recognition of a gain or loss on the transfer of nonfinancial assets that are currently evaluatingnot in a contract with a customer (for example, assets within the impactscope of Topic 360, Property, Plant, and Equipment, and intangible assets within the scope of Topic 350, Intangibles—Goodwill and Other) are amended to be consistent with the guidance on recognition and measurement (including the constraint on revenue) in this update.  Under the new guidance, on our condensed consolidated financial statements.

In August 2014,an entity should recognize revenue to depict the FASB issued ASU 2014-15, Presentationtransfer of Financial Statements—Going Concern (Subtopic 205-40): Disclosure of Uncertainties Aboutpromised goods or services to customers in an Entity’s Abilityamount that reflects the consideration to Continue as a Going Concern, which provides guidance on determining when and how to disclose going-concern uncertainties in the financial statements. The new standard requires management to perform interim and annual assessments of an entity’s ability to continue as a going concern within one year of the date on which the financial statementsentity expects to be entitled in exchange for those goods or services.  The amendments in ASU No. 2014-09 are issued. An entity must provide certain disclosures if conditions or events raise substantial doubt about the entity’s ability to continue as a going concern. This ASU applies to all entities and is effective for annual reporting periods endingbeginning after December 15, 2016 and2017, including interim periods thereafter, with earlywithin that reporting period. Early application is permitted for annual reporting periods beginning after December 31, 2016.  We do not believe the adoption permitted. Weof this update will have a material impact on our financial statements.


Note 5. Fair Value Measurements

Estimates of fair value for financial assets and liabilities are currently evaluatingbased on the impactframework established in the accounting guidance for fair value measurements.  The framework defines fair value, provides guidance for measuring fair value and requires certain disclosures.  The framework prioritizes a fair value hierarchy that requires an entity to maximize the use of observable inputs and minimize the use of unobservable inputs when measuring fair value.  The following three broad levels of inputs may be used to measure fair value under the fair value hierarchy:

·Level 1: Observable inputs such as quoted prices (unadjusted) in active markets for identical assets or liabilities.
·Level 2: Inputs other than quoted prices that are observable for the asset or liability, either directly or indirectly.  These include quoted prices for similar assets or liabilities in active markets and quoted prices for identical or similar assets or liabilities in markets that are not active.
·Level 3: Significant unobservable inputs that cannot be corroborated by observable market data and reflect the use of significant management judgment.  These values are generally determined using pricing models for which the assumptions utilize management's estimates of market participant assumptions.

If the inputs used to measure the financial assets and liabilities fall within more than one of the new guidancedifferent levels described above, the categorization is based on the lowest level input that is significant to the fair value measurement of the instrument.
On June 30, 2015 and March 31, 2015, the only asset or liability measured at fair value on a recurring basis was the long-term incentive plan accrual with a fair value of $398,000 and $730,000, respectively, considered a level 3 measurement. The long-term incentive plan began on October 2, 2014 and is described in note 9. The estimated fair value of the accrual is calculated on a quarterly basis using a Monte Carlo valuation model.  Vesting is based on the probability of meeting the stock price criteria, the probability of which is considered in determining the estimated fair value.

Remeasurements to fair value on a nonrecurring basis relate primarily to our property, plant and equipment and intangible assets and occur when the derived fair value is below their carrying value on our condensed consolidated financial statements.

Fair Value Measurements

Consolidated Balance Sheet.  As of June 30, 2015 and March 31, 2015 we had no remeasurements of such assets to fair value.


The carrying amounts reflectedreported in our condensed consolidated balance sheetsthe Condensed Consolidated Balance Sheets for cash and cash equivalents, accounts receivable, prepaid expenses andinventories, other current assets, accounts payable, accrued expenses, accrued compensation,liabilities and capital lease obligations approximate fair value due to their short-term nature. The carrying value of our convertible debt-related party approximatesapproximate fair value due to its attributes, which include, amongst others, interest and its conversion feature into common stock.

In determining the fair value of the convertible debt – related party, we analyzed its attributes (coupon rate, conversion price, and the percentage of market cap the face value of the debt instrument was prior to the announcement of the debt) as compared with public company convertible debt issuances in the healthcare industry. We determined the convertible debt was not issued at a discount as its fair value was equal to its face (carrying) value.


Concentration of Credit Risk

Concentration of credit risk with respect to accounts receivable relates to certain domestic and international customers to whom we make substantial sales. To reduce risk, we routinely assess the financial strength of our customers and, when appropriate, we obtain advance payments for our international sales. As a consequence, we believe that our accounts receivable credit risk exposure is limited. We maintain an allowance for potential credit losses, but historically we have not experienced any significant credit losses related to any individual customer or group of customers in any particular industry or geographic area.

The following table summarizes net sales to our significant customer, which accounted for more than 10% of total medical segment net sales and total accounts receivable, net:

  

Three Months Ended

  

Six Months Ended

 
  

September 30,

  

September 30,

 
  

2014

  

2013

  

2014

  

2013

 

Medical segment

                

Stryker

 $362  $1,201  $840  $2,346 

Percentage of total medical segment net sales

  11%  35%  13%  36%

Percentage of total net sales

  9%  30%  11%  31%

            
  As of September 30,  As of March 31,         
  

2014

  

2014

         

Percentage of total accounts receivable, net

  11%  27%        

Note 2.     Basic and Diluted Net Loss per Common Share

Basic net loss per share is calculated by dividing the net loss by the weighted average number of common shares outstanding. For all periods presented, the diluted net loss per common share is the same as basic net loss per common share, as the inclusion of other shares of stock issuable pursuant to stock options, warrants, and convertible debt would be anti-dilutive.

The following table summarizes equity securities that were excluded from the calculation of fully diluted loss per share as of September 30, 2014 and 2013, respectively:

  

September30,

 
  

2014

  

2013

 

Convertible debt

  22,401,050   16,666,666 

Stock options

  4,305,110   4,506,775 

Warrants

  1,880,620   1,880,620 

Restricted stock

  1,387,752   207,902 

Total anti-dilutive securities

  29,974,532   23,261,963 

Note 3.6. Inventories


Inventories are stated at the lower of cost (first-in, first-out method) or market using(net realizable value).  We value at lower of cost or market the first-in, first-out (“FIFO”) methodslow moving and obsolete inventories based upon current and expected future product sales and the expected impact of product transitions or modifications.  Historically, the inventory write-offs have generally been within our expectations. Inventories consist of the following:

  

September30,

2014

  

March 31,

2014

 

Raw materials

 $3,151  $3,456 

Work in process

  578   329 

Finished goods

  492   409 

Inventories, net

 $4,221  $4,194 


  June 30, 2015  March 31, 2015 
     
Raw materials $3,377,000  $3,156,000 
Work-in-process  658,000   527,000 
Finished goods  834,000   1,143,000 
         
  $4,869,000  $4,826,000 

Inventories acquired in a business combination are recorded at their estimated fair value less profit for sales efforts and expensed in cost of sales as that inventory is sold. On March 31, 2015, inventories included an adjustment amount of $240,000 related to VSCI inventory recorded at estimated fair value. During the three months ended June 30, 2015, $180,000 was recorded as an addition to cost of goods sold and on June 30, 2015, $60,000 of the adjustment amount remained, which will be recorded during the second fiscal quarter ending September 30, 2015.

Note 7. Net Loss per Common Share

We calculate basic net loss per common share amounts by dividing net loss by the weighted-average common shares outstanding, excluding outstanding shares contingently subject to forfeiture.  For calculating diluted net loss per common share amounts, we add additional shares to the weighted-average common shares outstanding for the assumed exercise of stock options and vesting of restricted shares, if dilutive.  Because we had a net loss during the three months ended June 30, 2015 and 2014 the following options and warrants and outstanding and unvested restricted stock to purchase shares of our common stock were excluded from diluted net loss per common share because of their anti-dilutive effect, and therefore, basic net loss per common share equals dilutive net loss per common share:

Number of
options, warrants and
unvested restricted
stock
Range of stock
option and warrant
exercise prices
June 30, 20152,638,000$1.64 to $24.40
June 30, 20141,604,000$0.77 to $2.63
 
Note 8. Shareholder’s Equity

Raw materials include components purchased from independent suppliers. Most purchased components are available from multiple sources, with

Share-based compensation.  On June 30, 2015, the exception of certain key components which are supplied to us by key suppliers, with whomCompany had one active plan, the Cogentix Medical 2015 Omnibus Incentive Plan, for share-based compensation grants (“the 2015 Plan”). Under the 2015 Plan, if we have long-term supply arrangements, but no long-term supply agreements.

Note4. Supply Agreements

a change in control, all outstanding grants, including those subject to vesting or other performance targets, fully vest immediately.  Under a three-year agreement with Stryker Corporation, or Stryker, that expiresthe 2015 Plan, we reserved 2,500,000 shares of our common stock for share-based grants and 1,502,587 shares remain available for grant on June 30, 2015.


We recognize share-based compensation expense in Decemberour Condensed Consolidated Statement of Operations based on the fair value at the time of grant of the share-based payment over the requisite service period.  We incurred approximately $225,000 and $323,000 in share-based compensation expense for the three months ended June 30, 2015 and 2014, respectively.

On June 30, 2015, we arehad approximately $1,103,000 of unrecognized share-based compensation expense, net of estimated forfeitures, related to stock options that we expect to recognize over a weighted-average period of approximately 1.75 years.  We also had $1,443,000 of unrecognized share-based compensation expense, net of estimated forfeitures, related to restricted shares that we expect to recognize over a weighted-average period of approximately 2.16 years.

We grant option awards with an exercise price equal to the exclusive supplierclosing market price of our stock at the date of the URT-7000 Video Ureteroscope, peripheralsgrant.  Options granted under this plan generally expire over a period ranging from five to seven years from date of grant and accessoriesvest at varying rates ranging up to Strykerthree years.

We determined the fair value of our option awards using the Black-Scholes option pricing model.  We used the following weighted-average assumptions to value the options granted during the three months ended June 30:

  20152014
   
Expected life in years3.843.47
Risk-free interest rate1.11%1.0%
Expected volatility63.94%68.43%
Expected dividend yield0%0%
Weighted-average grant date fair value$0.79$1.59

The expected life for options granted represents the period of time we expect options to be outstanding based on historical data of option holder exercise and termination behavior for similar grants.  The risk-free interest rate for periods within the contractual life of the option is based on the U.S. Treasury rate over the expected life at the time of grant.  Expected volatility is based upon historical volatility of our stock.  We estimate the forfeiture rate for stock awards to be approximately 10% for executive employees and directors and approximately 15% for non-executive employees for fiscal 2016 awards based on our historical experience.

The following table summarizes the activity related to our stock options during the three months ended June 30, 2015:

  Number of shares  Weighted average exercise price  Weighted average remaining life in years  Aggregate intrinsic value 
         
Outstanding at March 31, 2015  2,251,085  $5.32   5.06  $- 
Options granted  617,914   1.64         
Options exercised  -   -         
Options surrendered  (77,325)  6.16         
                 
Outstanding at June 30, 2015  2,791,674  $4.48   5.48  $- 
                 
Exercisable at June 30, 2015  1,661,379  $5.83   3.96  $- 

The total fair value of stock options that vested during the three months ended June 30, 2015 and 2014 was $55,000 and $95,000, respectively.
Our 2015 Plan also permits the compensation committee of our board of directors to grant other stock-based benefits, including restricted shares. The following table summarizes the activity related to our restricted shares during the three months ended June 30, 2015:

  Number of Shares  Weighted average grant date fair value  Weighted average remaining life in years  Aggregate intrinsic value 
Balance at March 31, 2015
  
317,741
  
$
4.47
   
1.93
  
$
387,644
 
Shares granted  379,499   1.64         
Shares vested  (97,223)  4.50         
Shares forfeited  -   -         
                 
Balance at June 30, 2015  600,017  $2.68   2.16  $972,027 

The aggregate intrinsic value shown above for the restricted shares represents the total pre-tax value based on the closing price of our common stock at the end of each period.

Stock Warrants-Related Party.  On June 30, 2015, the Company has warrants outstanding that were issued to Mr. Lewis C. Pell, a member of the Company’s board of directors, to purchase an aggregate of 376,123 shares of our common stock at a weighted average exercise price of $9.31 per share.  The duration in which the warrants may be exercised commences on the earlier of (i) March 31, 2018 or (ii) three days prior to the record date established for the declaration of any dividend or distribution of any rights in respect to our common stock in cash or other property other than our common stock, and terminates on the later of (x) the maturity date of the convertible promissory notes or (y) the date the convertible promissory notes are paid in full or converted into shares.  In addition, the warrants may be exercised immediately prior to a change in control.

Long-Term Incentive Plan and Awards.  On October 1, 2014, the compensation committee of our board of directors and our board of directors approved and adopted a Performance Award Agreement under the Uroplasty, Inc. 2006 Amended Stock and Incentive Plan, as amended, and on October 2, 2014, grants of Performance Awards (the “Awards”) were made to members of our senior management team.

Performance goals for the Awards are based on the achievement of specified stock price targets during the period beginning on the date of grant and ending on the fourth anniversary of the date of grant or, if earlier, the closing date of a change of control (as defined in the United States.

From April 2011 through May 2014, Stryker hadPlan) of the exclusive rights to marketCompany (the “Performance Period”).  The stock price targets under the Awards are: $7.57 price per share of common stock, $10.32 price per share of common stock and sell our cystoscopes, the CST- 5000 Video Cystoscope and the CST-4000 Fiber Cystoscope, and the accompanying EndoSheath disposables, peripherals and accessories, (the “Cystocscope Products”). We elected to not renew this exclusivity and to directly sell the Cystoscope Products in the U.S. We made this decision in large part because Stryker’s endoscopy sales force focuses$13.76 price per share of common stock.


A stock price target is considered achieved on the operating roomdate (a) the average closing price of a share of our common stock equals or exceeds a stock price target for at least 45 consecutive trading days or (b) of the consummation of a change of control of the Company, provided the closing price of a share of our common stock on the last trading day immediately preceding the closing date of the change of control equals or exceeds a stock price target not previously achieved during the Performance Period.

The Awards are accounted for as liability awards under the share-based compensation accounting guidance, as the awards are based on the performance of our common stock and are expected to be settled in hospitals, while most cystoscopy procedures are performed in physicians’ officescash.  Expense for the awards is recognized over the derived service period of approximately 2.4 years. We recorded a liability of $123,000 at June 30, 2015 and ambulatory surgical centers.

related expense was $(29,000) for the three months ended ending June 30, 2015 for the Awards.

Note 5.9. Convertible Debt – Related Party

Convertible Promissory Notes


The following table is a summary of our convertible debt – related party at Septemberon June 30, 2014:

Convertibledebt –relatedparty

 

Gross

Principal

Amount

Outstanding

  

Unamortized

Debt

Discount

  

Net Amount

Outstanding

 

Replacement Note

 $20,000  $-  $20,000 

2013 Note

  3,500   (1,020)  2,480 

2014 Note

  2,000   -   2,000 
  $25,500  $(1,020) $24,480 

Pursuant to the Prior Letter Agreement,2015:


  
Gross
Principal
Amount
  
Unamortized
Debt
Discount
  
Net
Amount
 
       
Note Payable A $20,000,000  $(4,021,808) $15,978,192 
             
Note Payable B  3,500,000   (620,944)  2,879,056 
             
Note Payable C  4,990,000   (1,051,784)  3,938,216 
  $28,490,000  $(5,694,536) $22,795,464 

The Convertible Debt-Related Party is held by Mr. Lewis C. Pell, agreed to provide financial assistance to us in the amount of up to $5.0 million, if necessary to support our operations, for a period ending on the earlier of (i) July 1, 2015 or (ii) our raising debt or equity capital in the amount of $5.0 million or more. The Prior Letter Agreement provided that this financial assistance, if drawn by us, would be in the form of an additional loan, share purchase, or financing transaction, on such terms as we and Mr. Pell may determine. The Prior Letter Agreement was terminated upon the issuancemember of the 2014 Note.

Pursuant to the Prior Letter Agreement, on June 16, 2014, or the 2014 Effective Date, we issued the 2014 Company’s board of directors, and consists of three convertible promissory notes.


Note with Mr. Pell that allowed us to borrow up to $5.0 million up to June 15, 2019. The 2014 NotePayable A accrues annual interest at the rate of 1.91%0.84%. The 2014 Note must be repaid in full on or before the fifth anniversary of the 2014 Effective Date, or the 2014 Maturity Date, but may be prepaid by us at any time without penalty. We will be required to repay all amounts outstanding under the 2014 Note upon an event of default, as defined in the 2014 Note. The outstanding principal amount of the 2014 Note Payable A is convertible at any time prior to the 2014 Maturity Date, at Mr. Pell’s option, into shares of our common stock at a price of $1.11, the closing bid price of our common stock on the 2014 Effective Date. At September 30, 2014, we had outstanding principal borrowings of $2.0 million under the 2014 Note, which is included in convertible debt – related party on our condensed consolidated balance sheet. Each time we draw on any available credit under the 2014 Note, we determine if a beneficial conversion feature of the convertible debt exists. A beneficial conversion feature will arise if the $1.11 conversion price of the 2014 Note is below the per share fair value of our common stock on the date of a drawdown.

On September 25, 2013, or the 2013 Effective Date, we entered into a convertible promissory note, or the 2013 Note, with Mr. Pell that allowed us to borrow up to $3.5 million. The 2013 Note accrues annual interest, at the rate of 1.66%. The 2013 Note must be repaid in full on or before the fifth anniversary of the 2013 Effective Date, or the 2013 Maturity Date, but may be prepaid by us at any time without penalty. We will be required to repay all amounts outstanding under the 2013 Note upon an event of default, as defined in the 2013 Note. The outstanding principal amount of the 2013 Note is convertible at any time prior to the 2013 Maturity Date, at Mr. Pell’s option, into shares of our common stock at a price of $0.89, the closing bid price of our common stock on the 2013 Effective Date. At September 30, 2014, we had outstanding principal borrowings of $3.5 million, gross of the amount recognized as a beneficial conversion feature, under the 2013 Note, which is included in Convertible debt – related party on our condensed consolidated balance sheet.


During each draw upon the 2013 Note, a beneficial conversion feature was recorded as a result of the market price of our common stock increasing after the 2013 Effective Date. The following table summarizes the unamortized beneficial conversion feature amounts recorded as of September 30, 2014:

Date

 

Borrowing

Amount

  

Convertible

Shares

  

Share Price

on

Borrowing

Date

  

Unamortized Beneficial

Conversion

 Feature

 

October 7, 2013

 $1,000   1,123,595  $0.95  $55 

November 26, 2013

  1,000   1,123,595   1.01   113 

January 21, 2014

  1,000   1,123,595   1.39   508 

March 13, 2014

  500   561,799   1.54   344 
  $3,500   3,932,584      $1,020 

The beneficial conversion feature amounts were recorded as a convertible debt discount with a corresponding increase to additional paid-in capital. The amounts are being amortized using the effective interest rate method from the borrowing date to the Maturity Date. At September 30, 2014, we expect to recognize the unamortized convertible debt discount balance of $1.0 million over a period of approximately four years.

On September 19, 2012, or the Replacement Note Effective Date, we entered into a convertible promissory note, or the Replacement Note, with Mr. Pell that allowed us to borrow up to $20.0 million. The Replacement Note (i) consolidated and restructured the $15.0 million in aggregate borrowings collectively outstanding under an Amended and Restated Loan Agreement, dated September 30, 2011, between us and Mr. Pell, or the Original Agreement, and a separate promissory note, dated July 25, 2012, between us and Mr. Pell, and (ii) provided for up to $5.0 million in additional borrowings.

The Replacement Note accrues annual interest, payable annually, at the rate of 0.84%. The Replacement Note must be repaid in full on or before the fifth anniversary of the Replacement Note Effective Date, or the Replacement Note Maturity Date, but may be prepaid by us at any time without penalty. We will be required to repay all amounts outstanding under the Replacement Note upon an event of default, as defined in the Replacement Note.

The outstanding principal amount of the Replacement Note is convertible at any time prior to the Replacement Note Maturity Date, at Mr. Pell’s option, into shares of our common stock at a conversion price of $1.20$6.00 per share, which was the closing bid price of our common stock on the Replacement Note Effective Date. At September 30, 2014, we had $20.0 million in outstanding principal borrowings under the Replacement Note, which is reflected as convertible debt – related party on our condensed consolidated balance sheet.

Pursuant to the Original Agreement, Mr. Pell received warrants to purchase an aggregate of 1,880,620 shares of our common stock at a weighted average exercise price of $1.86 per share. All of the warrants are vested and expire on the later of September 30, 2016 or one year after the termination of the Original Agreement and repayment of all amounts due and payable under the Original Agreement.

Amortization of the convertible debt discount and interest expense related to the accrued interest on outstanding borrowings are recorded as interest expense in our condensed consolidated statement of operations. Interest expense for the three months ended September 30, 2014 and 2013, respectively, was comprised of:

  

Three monthsended

  

Six months ended

 
  

September 30,

  

September 30,

 
  

2014

  

2013

  

2014

  

2013

 

Amortization of convertible debt discount

 $(40) $-  $(66) $- 

Interest expense

  (66)  (44)  (123)  (85)
  $(106) $(44) $(189) $(85)


At September 30, 2014, we had an aggregate amount of $376 thousand in accrued interest under the 2014

Note the 2013 Note and the Replacement Note, which is included in accrued expenses on our condensed consolidated balance sheet.

ExistingLetter Agreement

Pursuant to the Existing Letter Agreement, Mr. Pell has agreed to provide financial assistance to us in the amount of up to $2.5 million, if necessary to support our operations, for a period ending on the earlier of (i) January 1, 2016 or (ii) our raising debt or equity capital in the amount of $2.5 million or more. This financial assistance, if drawn by us, would be in the form of an additional loan, share purchase, or financing transaction, on such terms as we and Mr. Pell may determine. We have not utilized the Existing Letter Agreement.

Note6.Stock-Based Awards

We maintain the following stockholder-approved equity incentive plans:

The 2000 Stock Incentive Plan (the “2000 Plan”) authorized the issuance of up to 4,500,000 shares of common stock covering several different types of awards, including stock options, restricted shares, stock appreciation rights, and performance shares.

The 2007 Stock Incentive Plan (the “2007 Plan”) authorized the issuance of up to 5,000,000 shares of common stock covering several different types of awards, including stock options, restricted shares, stock appreciation rights, and other stock-based awards. On July 26, 2012, our stockholders approved an amendment to the 2007 Plan further increasing the number of authorized shares issuable under the plan to 7,000,000 shares of common stock.

The 2003 Director Option Plan (the “2003 Plan”) authorized the issuance of up to 450,000 shares of common stock covering the annual automatic grant, unless waived, of 10,000 stock options per outside director per year. The 2003 Plan also provides for granting newly elected or appointed outside directors a one-time grant of 10,000 stock options.

The stock option plans provide that options may be granted at an exercise price of 100% of fair market value of our common stock on the date of grant, may be exercised in full or in installments, at the discretion of our Board of Directors (the “Board”) or its Compensation Committee (the “Compensation Committee”), and must be exercised within ten years from date of grant. We recognize stock-based compensation expense on a straight-line basis over the requisite service period based on fair values, generally four years. We use historical data to estimate expected employee behaviors related to option exercises and forfeitures and included these expected forfeitures as a part of the estimate of stock-based compensation expense as of the grant date.


Stock Options

The following table summarizes stock options activity for the six months ended September 30, 2014:

  

Number

of Shares

  

Exercise

Price Range

  

Weighted

Average

ExercisePrice

  

Weighted

Average

Remaining

ContractualLife

 

Outstanding at April 1, 2014

  4,377,874  $0.85 $4.88  $1.78   6.0 

Granted

  830,000  0.90 1.25   1.06     

Exercised

  (25,000

)

 0.97 0.97   0.97     

Canceled

  (877,764

)

 0.95 4.30   2.40     

Outstanding at September 30, 2014

  4,305,110  $0.85 $4.88  $1.52   6.4 

Vested and expected to vest at September 30, 2014

  4,262,557  $0.85 $4.88  $1.53   6.4 

Exercisable at September 30, 2014

  3,260,194  $0.85 $4.88  $1.64   5.5 

The weighted average fair value of options granted during the six months ended September 30, 2014 and 2013 was $0.73 and $0.68 per share, respectively.

The total intrinsic value (the excess of the market price over the exercise price) was approximately $12 thousand for stock options outstanding, $10 thousand for stock options exercisable, and $12 thousand for stock options vested and expected to vest as of September 30, 2014. The total intrinsic value for stock options exercised during the six months ended September 30, 2014 was approximately $5 thousand. There were no stock options exercised during the six months ended September 30, 2013.

We do not expect to realize any tax benefits from future disqualifying dispositions, if any. 

RestrictedStock

We determine stock-based compensation expense for performance based restricted stock based upon the fair value of our common stock at the date of grant and recognize expense based upon the most probable outcome as to whether the performance targets will be achieved and the stock-based compensation being earned.

The following table summarizes restricted stock activity for the six months ended September 30, 2014:

  

Number

of Shares

  

Weighted

Average

Grant Price

 

Nonvested at April 1, 2014

  1,325,402  $1.06 

Granted

  473,605   1.08 

Vested

  (91,450)  1.38 

Forfeited

  (319,805)  1.05 

Nonvested at September 30, 2014

  1,387,752  $1.05 

We grant restricted stock awards to certain executive officers, certain management employees and certain members of our Board. 


Stock-Based Compensation Expense

We estimated the fair value of the stock options granted on the date of grant using a Black-Scholes valuation model that used the weighted average assumptions noted in the following table. The risk-free interest rate assumption we use is based upon United States Treasury interest rates appropriate for the expected life of the awards. The expected life (estimated period of time that we expect employees, consultants and directors to hold their stock options) was estimated based on historical rates for two group classifications, (i) employees and consultants and (ii) outside directors. Expected volatility was based on historical volatility of our stock price for a period equal to the stock option’s expected life and calculated on a daily basis. The expected dividend rate is zero since we do not currently pay cash dividends on our common stock and do not anticipate doing so in the foreseeable future.

  

Three Months Ended

September 30,

  

Six Months Ended

September 30,

 
  

2014

  

2013

  

2014

  

2013

 

Risk-free interest rate

  2.0

%

  1.4

%

  2.0

%

  1.2

%

Expected life (in years)

  6.5   5.1   6.6   5.5 

Expected volatility

  78

%

  75

%

  77

%

  80

%

Expected dividend yield

  --   --   --   -- 

The following table summarizes stock-based compensation recorded in our condensed consolidated statements of operations for the three and six months ended September 30, 2014 and 2013, respectively:

  

Three Months Ended

  

Six Months Ended

 
  

September 30,

  

September 30,

 
  

2014

  

2013

  

2014

  

2013

 

Cost of sales

 $22  $12  $38  $42 

Selling, general and administrative expenses

  166   (244)  289   265 

Research and development expenses

  7   5   22   21 

Total stock-based compensation expense

 $195  $(227) $349  $328 

At September 30, 2014, unrecognized stock-based compensation expense related to stock options was approximately $0.7 million and is expected to be recognized over a weighted average period of approximately 3.2 years, while unrecognized stock-based compensation expense related to nonvested (restricted stock) awards was approximately $0.5 million, which is expected to be recognized over a weighted average period of approximately 3.0 years.

Note 7.Treasury Stock

The following table summarizes treasury stock activity for the six months ended September 30, 2014 and 2013:

Six Months Ended

 

Number

of Shares

Repurchased

  

Cost

  

Weighted

Average

Purchase

Price

 

September 30, 2014

  6  $7  $1.22 
             

September 30, 2013

  26  $28  $1.11 

The shares were purchased from certain management employees to cover income tax withholdings upon the lapse of restrictions on their restricted stock awards.

Note 8.Segment Information

We have two reportable segments, medical and industrial. Each of these operating segments has unique characteristics. Management evaluates the revenue and profitability performance of each of our product lines to make operating and strategic decisions. We have no intersegment revenue.

Our medical segment designs, develops, manufactures, and markets our advanced line of endoscopy-based products, including our state-of-the-art flexible endoscopes, and our EndoSheath technology (referred to as a sheath or EndoSheath disposable) for a variety of specialties and markets.


Our industrial segment, through our wholly-owned subsidiary Machida, designs, manufactures, and sells borescopes to a variety of users, primarily in the aircraft engine manufacturing and aircraft engine maintenance industries. A borescope is an instrument that uses optical fibers for the visual inspection of narrow cavities. Our borescopes are used to inspect aircraft engines, casting parts and ground turbines, among other items.

The following table presents key financial highlights, by reportable segments:

Three Months EndedSeptember 30, 2014

 

Medical

  

Industrial

  

Adjustments*

  

Consolidated

 

Net sales

 $3,267  $843  $-  $4,110 

Gross profit

  1,023   235   -   1,258 

Operating loss

  (1,435

)

  (6

)

  -   (1,441

)

Interest expense, net

  (106)  -   -   (106)

Depreciation and amortization

  151   1   -   152 

Stock-based compensation expense

  186   9   -   195 

Expenditures for fixed assets

  (8)  -   -   (8)
                 

As of September 30, 2014

                

Total assets

  10,542   1,865   (2,358

)

  10,049 
                 

Three Months EndedSeptember 30, 2013

                

Net sales

 $3,399  $569  $-  $3,968 

Gross profit

  981   214   -   1,195 

Operating loss

  (1,345

)

  62   -   (1,283

)

Interest expense, net

  (44)  -   -   (44)

Depreciation and amortization

  170   3   -   173 

Stock-based compensation expense

  (221

)

  (6)  -   (227

)

Expenditures for fixed assets

  46   -   -   46 
                 

As of September 30, 2013

                

Total assets

  11,240   1,333   (1,840

)

  10,733 

SixMonths EndedSeptember 30, 2014

 

Medical

  

Industrial

  

Adjustments*

  

Consolidated

 

Net sales

 $6,327  $1,535  $-  $7,862 

Gross profit

  1,921   486   -   2,407 

Operating loss

  (3,273

)

  (46

)

  -   (3,319

)

Interest expense, net

  (189)  -   -   (189)

Depreciation and amortization

  314   4   -   318 

Stock-based compensation expense

  328   21   -   349 

Expenditures for fixed assets

  17   -   -   17 
                 

Six Months EndedSeptember 30, 2013

                

Net sales

 $6,428  $1,192  $-  $7,620 

Gross profit

  1,774   501   -   2,275 

Operating loss

  (3,732

)

  60   -   (3,672

)

Interest expense, net

  (85)  -   -   (85)

Depreciation and amortization

  355   7   -   362 

Stock-based compensation expense

  309   19   -   328 

Expenditures for fixed assets

  46   -   -   46 


  

As of September 30,

 

* Adjustments

 

2014

  

2013

 

Intercompany eliminations

 $(1,672

)

 $(1,154

)

Investment in subsidiaries

  (686

)

  (686

)

Total adjustments

 $(2,358

)

 $(1,840

)

Note 9.Subsequent Events

On October 24, 2014, we drew down another $1.0 million under the 2014 Note. As of November 13, 2014, we had $3.0 million in principal outstanding under the 2014 Note.


Item 2. Managements Discussion and Analysis of Financial Condition and Results of Operations

Executive Summary

Business Overview

Vision-Sciences, Inc. and its subsidiaries, or the Company, or our, us, or we, designs, develops, manufactures, and markets products for endoscopy – the science of using an instrument, known as an endoscope, to provide minimally invasive access to areas not readily visible to the human eye. We operate in two segments: medical and industrial.

Medical Business Segment

Our medical segment designs, manufactures, and sells our advanced line of endoscopy-based products, including our flexible fiber and video endoscopes and our EndoSheath technology, for a variety of specialties and markets. Our proprietary reusable flexible endoscope is combined with a single-use, sterile protective EndoSheath disposable that is placed over the patient contact area of the scope. Our “always sterile” EndoSheath technology reduces the risks of cross-contamination associated with the reuse (or “reprocessing”) of conventional endoscopes, which are difficult, costly, and time-consuming to clean and disinfect or sterilize.

We target five market spaces for our endoscopes and our EndoSheath technology:

Urology – we manufacture, market, and sell our video and fiber cystoscopes, digital processing units, EndoSheath technology, peripherals and accessories to urologists. We also supply our video ureteroscopes to the Endoscopy Division of Stryker Corporation, or Stryker.

Pulmonology (Critical Care)– we manufacture, market, and sell our video and fiber bronchoscopes (an endoscope that allows detailed viewing of the lungs), digital processing units, EndoSheath technology, peripherals and accessories to intensivists, pulmonologists, thoracic surgeons, and other airway-related physicians.

Surgery– we manufacture, market, and sell our TNE (trans-nasal esophagoscopy) video endoscope, digital processing units, EndoSheath technology, peripherals and accessories to general surgeons, primarily bariatric and gastroesophageal reflux disease (“GERD”) surgeons.

Gastroenterology – we manufacture, market, and sell our TNE video endoscope, digital processing units, EndoSheath technology, peripherals and accessories to gastroenterology (“GI”) physicians, ear, nose, and throat (“ENT”) physicians and others with a GI focus as part of their practice.

ENT (ear, nose, and throat) – we manufacture, market, and sell our ENT video and fiber endoscopes, digital processing units, peripherals and accessories to ENT physicians and speech pathologists.

All of our products, with the exception of our ureteroscopes, are sold directly by our sales force in the United States, and by international distributors in the rest of the world. Our ureteroscopes are sold to Stryker, who then distributes them in the United States.

From April 2011 through May 2014, Stryker had the rights to market and sell our cystoscopes, the CST- 5000 Video Cystoscope and the CST-4000 Fiber Cystoscope, and the accompanying EndoSheath technology, peripherals and accessories. We decided to not renew this exclusivity and to directly sell the cystoscopes, their EndoSheaths, peripherals and accessories in the U.S. to maximize our revenue and margins. We made this decision in large part because Stryker’s endoscopy direct sales force focuses on the operating room in hospitals, while most cystoscopy procedures are performed in physicians’ offices and ambulatory surgical centers. We believe that our U.S. sales force will be able to maximize revenue potential by focusing on these call points (physicians’ offices and ambulatory surgical centers). We expect that we will benefit by realizing the full gross profit contribution, which was previously shared with Stryker.

Our goal is to become a customer-centric organization with a focus on enhancing stockholder value. We are doing this by:

Increasing the competencies and capabilities of our sales force in the U.S. by adding proven medical-surgical device sales professionals and expanding our international distribution network in promising territories;

Targeting office-based clinics and ambulatory surgical centers, as well as acute care facilities, that recognize patient safety and the patient experience as a primary value position;


Capitalizing on our extensive and relevant library of published clinical studies and peer reviewed papers on the efficacy and safety of our EndoSheath technology; and

Enhancing our professional educational programs to allow healthcare professionals to teach other healthcare professionals about our EndoSheath technology.

Industrial Business Segment

Our industrial segment, through our wholly-owned subsidiary Machida, designs, manufactures, and sells borescopes to a variety of users, primarily in the aircraft engine manufacturing and aircraft engine maintenance industries. A borescope is an instrument that uses optical fibers for the visual inspection of narrow cavities.  Our borescopes are used to inspect aircraft engines, casting parts and ground turbines, among other items.

Machida’s quality line of borescopes includes a number of advanced standard features normally found only in custom designed instruments. We were the first to offer a flexible borescope with a grinding attachment, allowing users to “blend” or smooth small cracks in turbine blades of jet engines without disassembling the engine, saving our customers significant expense and delay.

Debt Arrangements – Related Party

Convertible Promissory Notes

Pursuant to a May 29, 2014 letter agreement between us and Mr. Lewis C. Pell, our Chairman, or the Prior Letter Agreement, Mr. Pell agreed to provide financial assistance to us in the amount of up to $5.0 million, if necessary to support our operations, for a period ending on the earlier of (i) July 1, 2015 or (ii) our raising debt or equity capital in the amount of $5.0 million or more. The Prior Letter Agreement provided that this financial assistance, if drawn by us, would be in the form of an additional loan, share purchase, or financing transaction, on such terms as we and Mr. Pell may determine. The Prior Letter Agreement was terminated upon the issuance of the 2014 Note (as defined below).

On June 16, 2014, or the 2014 Effective Date, we entered into a convertible promissory note, or the 2014 Note, with Mr. Pell, in accordance with the Prior Letter Agreement. The 2014 Note accrues annual interest at the rate of 1.91%. The 2014 Note must be repaid in full on or before the fifth anniversary of the 2014 Effective Date, or the 2014 Maturity Date, but may be prepaid by us at any time without penalty. We will be required to repay all amounts outstanding under the 2014 Note upon an event of default, as defined in the 2014 Note. The outstanding principal amount of the 2014 Note is convertible at any time prior to the 2014 Maturity Date, at Mr. Pell’s option, into shares of our common stock at a price of $1.11, the closing bid price of our common stock on the 2014 Effective Date. As of September 30, 2014, we had outstanding principal borrowings of $2.0 million under the 2014 Note, which is included in convertible debt – related party on our condensed consolidated balance sheet. On October 24, 2014, we drew down another $1 million under the 2014 Note.

On September 25, 2013, or the 2013 Effective Date, we entered into a convertible promissory note, or the 2013 Note, with Mr. Pell that allowed us to borrow up to $3.5 million. The 2013 NotePayable B accrues annual interest at the rate of 1.66%. The 2013 Note must be repaid in full on or before the fifth anniversary of the 2013 Effective Date, or the 2013 Maturity Date, but may be prepaid by us at any time without penalty. We will be required to repay all amounts outstanding under the 2013 Note upon an event of default, as defined in the 2013 Note. The outstanding principal amount of the 2013 Note Payable B is convertible at any time prior to the 2013 Maturity Date, at Mr. Pell’s option, into shares of our common stock at a price of $0.89, the closing bid price of our common stock on the 2013 Effective Date. At September 30, 2014, we had outstanding principal borrowings of $3.5 million, gross of the amount recognized as a beneficial conversion feature, under the 2013 Note, which is included in convertible debt – related party on our condensed consolidated balance sheet.

On September 19, 2012, or the Replacement Note Effective Date, we entered into a convertible promissory note, or the Replacement Note, with Mr. Pell that allowed us to borrow up to $20.0 million. The Replacement Note (i) consolidated and restructured the $15.0 million in aggregate borrowings collectively outstanding under an Amended and Restated Loan Agreement, dated September 30, 2011, between us and Mr. Pell, or the Original Agreement, and a separate promissory note, dated July 25, 2012, between us and Mr. Pell, and (ii) provided for up to $5.0 million in additional borrowings.


The Replacement Note accrues annual interest, payable annually, at the rate of 0.84%. The Replacement Note must be repaid in full on or before the fifth anniversary of the Replacement Note Effective Date, or the Replacement Note Maturity Date, but may be prepaid by us at any time without penalty. We will be required to repay all amounts outstanding under the Replacement Note upon an event of default, as defined in the Replacement Note.

The outstanding principal amount of the Replacement Note is convertible at any time prior to the Replacement Note Maturity Date, at Mr. Pell’s option, into shares of our common stock at a conversion price of $1.20$4.45 per share, which wasshare.


Note Payable C accrues annual interest at the closing bid pricerate of 1.91%. The outstanding principal amount of Note Payable C is convertible into shares of our common stock on the Replacement Note Effective Date. at a conversion price of $5.55 per share.

At SeptemberJune 30, 2014, we had $20.0 million in outstanding principal borrowings under the Replacement Note, which is reflected as convertible debt – related party on our condensed consolidated balance sheet.

At September 30, 2014,2015, we had an aggregate amount of $376 thousand$599,954 in accrued interest under the 2014 Note, the 2013 Note and the Replacement Note,convertible notes payable, which is included in accrued expenses on our condensed consolidated balance sheet.

During


The convertible promissory notes mature on March 31, 2020 or earlier upon a change of control (as defined).  The convertible promissory notes generally cannot be converted prior to March 31, 2018. The convertible promissory notes may be converted earlier prior to a change in control or in connection with our prepayment of the convertible promissory notes.  The convertible promissory notes may be prepaid, at our option and upon 15 days’ notice to Mr. Pell, without other premium or penalty, with a combination of cash and common stock.  Interest on the convertible promissory notes is payable on the maturity date or upon repayment or conversion of all or any portion of the principal under the note.

Under purchase accounting for the merger, the convertible promissory notes were recorded at fair value on the merger date, resulting in a discount from their face value of $5,960,000. The discount is being amortized over the remaining term based on the effective interest rate method with an imputed interest rate of 4.72%.

Note 10. Savings and Retirement Plans

We sponsor various retirement plans for eligible employees in the United States, the United Kingdom, and The Netherlands. Our retirement savings plan in the United States conforms to Section 401(k) of the Internal Revenue Code and participation is available to substantially all employees. We may also make discretionary contributions ratably to all eligible employees. We made discretionary contributions to the U.S. plan of $70,000 and $72,000 for the three months ended June 30, 2015, and 2014, respectively.

Our international subsidiaries have defined benefit retirement plans for eligible employees.  These plans provide benefits based on the employee’s years of service and compensation during the years immediately preceding retirement, termination, disability, or death, as defined in the plans.

The cost for our defined benefit retirement plans in The Netherlands and the United Kingdom includes the following components for the three month period ended June 30:
  
Three Months Ended
June 30
 
  2015  2014 
     
Gross service cost $36,000  $36,000 
Interest cost  24,000   37,000 
Expected return on assets  (19,000)  (27,000)
Amortization  7,000   1,000 
Net periodic retirement cost $48,000  $47,000 
Note 11. Business Segment Information

ASC 280, “Segment Reporting,” establishes disclosure standards for segments of a company based on management’s approach to defining operating segments.  Reportable segments are defined primarily by the nature of products and services, the nature of the production processes, and the type of customers for our products and services.

We operate in two markets, the medical market and the industrial market.  Within the medical market, we have a number of product lines, endoscopy-based products, including flexible fiber and video endoscopes used in the practices of urology, pulmonology, trans-nasal esophagoscopy and ENT (ear, nose and throat) and a proprietary sterile disposable microbial barrier, known as EndoSheath technology, the Urgent PC® Neuromodulation System (“Urgent PC System”) a minimally-invasive, neuromodulation system that delivers percutaneous tibial nerve stimulation for office-based treatment of overactive bladder and associated symptoms; and Macroplastique® Implants (“Macroplastique”), an injectable, urethral bulking agent for the treatment of adult female stress urinary incontinence.

None of the industrial market sales, net losses or assets are more than 10% of our total sales, losses or assets.  Therefore, we aggregate our operating segments into one reportable segment in accordance with the objectives and principles of the applicable guidance.

For the three months ended June 30, 2015, no country other than the United States represented more than 10% of our consolidated revenue.  Information regarding net sales to customers by geographic area for the three months ended June 30, 2014 is as follows:

  
United
States
  United Kingdom  
All Other Foreign
Countries (1)
  Consolidated 
         
Three months ended June 30, 2014 $4,533,000  $697,000  $1,155,000  $6,385,000 
(1)No other country accounts for 10% or more of the consolidated net sales.

Information regarding geographic area in which we maintain long-lived assets is as follows:

  
United
States
  
All Other Foreign
Countries (1)
  Consolidated 
       
June 30, 2015 $1,482,000  $488,000  $1,970,000 
             
March 31, 2015 $1,397,000  $475,000  $1,872,000 

(1)Substantially all maintained in The Netherlands

Accounting policies of the operations in the various geographic areas are the same as those described in Note 1.  Net sales attributed to each draw upongeographic area are net of intercompany sales.  No single customer represents 10% or more of our consolidated net sales.  Long-lived assets consist of property, plant and equipment.
ITEM 2.  MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

Forward-looking Statements

We recommend that you read this quarterly report on Form 10-Q in conjunction with our annual report on Form 10-K for the 2013 Note,fiscal year ended March 31, 2015.

You should read the following discussion of our financial condition and results of operation together with the unaudited consolidated financial statements and the notes thereto included elsewhere in this report and other financial information included in this report.  The following discussions may contain predictions, estimates and other forward-looking statements that involve a beneficial conversion featurenumber of risks and uncertainties, as we discussed in our special note regarding “Forward-Looking Statements” beginning on page 3 of this report and under “Part I - Item 1A. Risk Factors” in our annual report on Form 10-K for the fiscal year ended March 31, 2015 and “Part II - Item 1A. Risk Factors” in this report.  These risks could cause our actual results to differ materially from any further performance suggested below.

We do not undertake, nor assume any obligation, to update any forward-looking statement that we may make from time to time.

Overview

Cogentix Medical, Inc. is a global medical device company headquartered in Minnetonka, Minnesota, with additional operations in New York, Massachusetts, The Netherlands and the United Kingdom. We design, develop, manufacture and market innovative proprietary technologies serving the urology, urogynecology/gyn, ENT (ear, nose and throat) and gastrointestinal markets. The Urgent® PC Neuromodulation System is an FDA-cleared device that delivers percutaneous tibial nerve stimulation (PTNS) for the office-based treatment of overactive bladder (OAB). The FDA-cleared EndoSheath® Systems combine state-of-the-art endoscopic technology with a sterile, disposable microbial barrier, providing practitioners and healthcare facilities with a solution to meet the growing need for safe, efficient and cost-effective flexible endoscopy. In the U.S. and worldwide, the Company also offers Macroplastique®, a urethral bulking agent for the treatment of stress urinary incontinence. Outside the U.S., the company markets additional bulking agents: PTQ® for the treatment of fecal incontinence and VOX® for vocal cord augmentation.

The Company is the result of the March 31, 2015 merger of two medical device companies, Uroplasty, Inc. and Vision-Sciences, Inc. The merger was recordedaccounted for as a reverse acquisition due to a number of factors including the relative voting interests in the combined company of the former Vision-Sciences and Uroplasty stockholders following the merger.  As a result, Uroplasty and its consolidated subsidiaries represent the accounting acquirer in the merger, and Vision and its consolidated subsidiary represent the legal acquirer in the merger.  Accordingly, while Vision was the legal acquirer in the merger, Uroplasty is treated as the acquiring company in the merger for accounting purposes.

As a result of the market pricemerger, our financial statements prior to March 31, 2015 are the historical financial statements of Uroplasty, and our common stock increasingfinancial statements on and after March 31, 2015 reflect the Effective Date. The beneficial conversion feature amounts were recorded asresults of the operations of Uroplasty and Vision-Sciences on a convertible debt discount with a corresponding increase to additional paid-in capital. The amounts are being amortized over a five-year period from the borrowing date to the Maturity Date. At September 30, 2014, the unamortized convertible debt discount balance was $1.0 million and is expected to be recognized over a period of approximately 4.0 years.

The following table is a summary of our convertible debt – related party at September 30, 2014:

Convertible debt – related party

 

Gross

Principal

Amount

Outstanding

  

Unamortized

Debt

Discount

  

Net Amount

Outstanding

 

Replacement Note

 $20,000  $-  $20,000 

2013 Note

  3,500   (1,020)  2,480 

2014 Note

  2,000   -   2,000 
  $25,500  $(1,020) $24,480 

The scheduled maturities of principal amounts of our Convertible debt – related party at September 30, 2014 were $20.0 million due September 19, 2017, $3.5 million due September 25, 2018 and $2.0 million due June 16, 2019.

ExistingLetter Agreement

Pursuant to a letter agreement dated October 28, 2014 with Mr. Pell, or the Existing Letter Agreement, Mr. Pell has agreed to provide financial assistance to us in the amount of up to $2.5 million, if necessary to support our operations, for a period ending on the earlier of (i) January 1, 2016 or (ii) our raising debt or equity capital in the amount of $2.5 million or more. This financial assistance, if drawn by us, would be in the form of an additional loan, share purchase, or financing transaction, on such terms as we and Mr. Pell may determine. We have not utilized the Existing Letter Agreement.

combined basis.


Critical Accounting Policies and Estimates

The preparation of


We prepare our condensed consolidated financial statements requires managementin accordance with U.S. generally accepted accounting principles, or GAAP, which require us to make estimates and assumptions in certain circumstances that affect the amounts reported in thereported.  In preparing these consolidated financial statements, and accompanying notes. Management evaluates thesewe have made our best estimates and assumptionsjudgments of certain amounts, giving due consideration to materiality.

We have identified in our annual report on Form 10-K for the fiscal year ended March 31, 2015, our “critical accounting policies,” which are certain accounting policies that we consider important to the portrayal of our results of operations and financial condition and which may require the application of a higher level of judgment by our management, and as a result are subject to an ongoing basis. Estimatesinherent level of uncertainty.  Management made no significant changes to our critical accounting policies during the three months ended June 30, 2015.
Results of Operations

Three months ended June 30, 2015 compared to three months ended June 30, 2014

The reported operations for the three months ended June 30, 2015 are based on historical experience, when available, and on various other assumptions that are believed to be reasonable under the circumstances, the results of which formCogentix, while the basisreported operations for making judgments about the carrying valuesthree months ended June 30, 2014 only include the results of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates underUroplasty.   Therefore, starting in the first quarter of fiscal 2016, our reported numbers will be materially different assumptions or conditions.

Management believes that, of its significant accounting policies, an understandingthan the reported numbers of the following critical accounting policies is important in obtaining an overall understanding of the condensed consolidated financial statements.


Revenue Recognition

We recognize revenue in accordance with the Financial Accounting Standards Board (the “FASB”) Accounting Standards Codification (“ASC”) 605 (Topic 605, Revenue Recognition). ASC 605 requires that five basic criteria must be met before revenue can be recognized:

1.     persuasive evidence that an arrangement exists;

2.     delivery has occurred or services were rendered;

3.     the fee is fixed and determinable;

4.     collectability is reasonably assured; and

5.     the fair value of undelivered elements, if any, exists.

Determination of criterion (4) above is based on management’s judgment regarding the collectability of invoices for products and services delivered to customers. Should changes in conditions cause management to determine this criterion is not met for certain future transactions, revenue recognized for any reporting period could be adversely affected. We recognize revenue when title passes to the customer, generally upon shipment of our products F.O.B. shipping point. Revenue for service repairs of equipment is recognized after service has been completed, and service contract revenue is recognized ratably over the term of the contract.

For products sold to Stryker we recognize revenue in a two-step process. The first step is recognition of revenue for our cost to manufacture these products when title passes to Stryker, generally upon shipment of our products F.O.B. shipping point. The second step is recognition of revenue for our specified margin of Stryker’s gross profit after Stryker sells the products to its end customers, based upon reports received from Stryker monthly. Stryker is not required to purchase any required minimum amount of products from us.

Stock Based Compensation

We account for stock-based awards issued to employees in accordance with the provisions of ASC 718 (Topic 718, Compensation – Stock Compensation). We recognize stock-based compensation expense on a straight-line uniform basis over the servicesame period of the award,prior years.


Net Sales:  During the three months ended June 30, 2015, consolidated net sales of $11,150,000 represented a $4,766,000, or a 75% increase, over net sales of $6,384,000 for the three months ended June 30, 2014. The increase in consolidated net sales for the three months ended June 30, 2015 was due to the merger with Vision-Sciences.  The revenue for the products from Vision-Sciences totaled $4,242,000 in the three months ended June 20, 2015.  The remainder of the increase is primarily due to the increase in revenue from Urgent PC.

Net sales to customers in the U.S. of $8,412,000 during the three months ended June 30, 2015, represented an increase of $3,788,000, or 82%, over net sales of $4,624,000 for the three months ended June 30, 2014. This increase is due to $2,994,000 of revenue in the three months ended June 30, 2015 from the Vision-Sciences products and $796,000 increase in domestic Urgent PC revenue.

Net sales to customers outside the U.S. for the three months ended June 30, 2015 increased $886,000 or 48% to $2,738,000, compared to $1,852,000 for the three months ended June 30, 2014. This increase is due to $1,248,000 of revenue in the three months ended June 30, 2015 from the Vision-Sciences products offset by a decrease in Urgent PC and Macroplastique of $362,000.  Approximately three quarters of the decrease in international Urgent PC and Macroplastique revenue is due to changes in foreign currency exchange rates.

Global revenue from Urgent PC totaled $4,684,000, representing a $624,000 increase, or 15%, over net sales of $4,060,000 for the three months ended June 30, 2014.  Global revenue from endoscopes and EndoSheath technology (inclusive of service and peripherals revenue) totaled $3,750,000  in the three months ended June 30, 2015, which is generally four yearsall incremental over the same period in the prior year as the merger occurred on March 31, 2015.  Global Macroplastique revenue totaled $1,941,000, a decrease of $138,000 or 4% for employees. We use historical datathe comparable period in the prior fiscal year.

Net sales in the U.S. of our Urgent PC System increased 26% to estimate expected employee behaviors$3,900,000 for the three months ended June 30, 2015, up from $3,100,000 for the same period last year.  Net sales increased as a result of improved sales execution within the U.S, an increase in the number of active customers and higher utilization per customer.

Urgent PC System sales to customers outside of the U.S. were $758,000 for the three months ended June 30, 2015, a decrease of $172,000 or 18% from the same quarter of the prior year.  The decrease in sales is attributed to changes in foreign currency exchange rates as well as lower unit sales in the international markets.

Net sales in the U.S. of our Endoscope and Endosheath technology (inclusive of service and peripherals revenue) totaled $2,628,000, which is all incremental over the same quarter of the prior year.  Net sales internationally for these products totaled $1,122,000 for the three months ended June 30, 2015.

Net sales in the U.S. of Macroplastique increased 6% to $1,448,000 for the three months ended June 30, 2015, up from $1,373,000 for the same period last year.  International net sales of Macroplastique totaled $493,000, a decrease of $213,000 or 30% from the same quarter last year. The decrease in sales is attributed to changes in foreign currency exchange rates as well as lower unit sales in the international markets.

Gross Profit:  Gross profit was $7,497,000, or 67.2% of net sales during the three months ended June 30, 2015, and $5,593,000, or 87.6% of net sales for the three months ended June 30, 2014.  The decrease in gross profit percentage for the three month period ended June 30, 2015 is attributed primarily to the addition of the Vision-Sciences products which have lower margins than the Uroplasty products.

General and Administrative Expenses (G&A):  G&A expenses of $2,159,000 during the three months ended June 30, 2015, increased $582,000 from $1,577,000 during the same period in 2014. The three month period ended June 30, 2015 included $266,000 for expenses related to option exercisesthe merger with Vision-Sciences and forfeituresthe inclusion of the G&A expenses of Vision-Sciences, offset by cost synergies related to the merger including lower headcount, lower legal and include these expected forfeituresaccounting and lower public company costs.

Research and Development Expenses (R&D):  R&D expenses of $1,074,000 during the three months ended June 30, 2015 increased $165,000 from $909,000 during the same period in 2014.  The increase is attributed primarily to the merger with Vision-Sciences, offset partially by lower personnel costs and lower expenditure on R&D projects.
Selling and Marketing Expenses (S&M):  S&M expenses of $6,843,000 during the three months ended June 30, 2015, increased $1,570,000, from $5,273,000, during the same period in 2014.  The increase is attributed primarily to an increase in sales personnel costs from the merger with Vision-Sciences and also includes $192,000 of merger related expenses.

Amortization of Intangibles: Amortization of intangibles was $634,000 and $8,000 for the three months ended June 30, 2015 and 2014, respectively.   The increase is due to the establishment of $13,660,000 of intangible assets as a part of the estimateallocation of stock-based compensation expense aspurchase accounting.  These intangible assets are amortized over a weighted average life of the grant date. For stock-based awards with performance-based vesting conditions, we are also required to estimate the probability of the vesting conditions being met. Stock-based awards issued to consultants are accounted for in accordance with the provisions of ASC 718 and ASC 505-50 (Subtopic 50 “Equity-Based Payments to Non-Employees” of Topic 505, Equity). Options granted to consultants are periodically revalued as the options vest, and are recognized as an expense over the related period of service or the vesting period, whichever is longer. Under the provisions of ASC 718, members of the Board are considered employees for calculation of stock-based compensation expense.

Allowance for Doubtful Accounts

We maintain an allowance for doubtful accounts for estimated losses resulting from the inability of our customers to make required payments. This allowance is used to report trade receivables at estimated net realizable value. We rely on prior experience to estimate cash that ultimately will be collected from the gross receivables balance at period-end. We maintain a specific allowance for customer accounts that will likely not be collectible due to customer liquidity issues. We also maintain an allowance for estimated future collection losses on existing receivables, determined based on historical trends.

Inventories

Inventories are stated at the lower of cost or market using the first-in, first-out (“FIFO”) method. If cost exceeds market, inventory is reported at its estimated fair market value based upon our historical experience with inventory becoming obsolete due to age, changes in technology, and other factors. We record a write-down for inventories of components that have become obsolete, slow moving, or are in excess of anticipated demand or net realizable value. We perform a detailed review of inventory each fiscal quarter that considers multiple factors, including demand forecasts, product life cycle status, product development plans, and current sales levels. Inventories consist of raw materials, work in process, and finished goods.

approximately 6 years.

Beneficial Conversion Feature

We account for beneficial conversion features in accordance with the provisions of ASC 470-20 (Subtopic 20 “Debt with Conversions and Other Options” of Topic 470, Debt). A beneficial conversion feature exists if the fair value of the underlying common stock is above the conversion price of the instrument on the commitment date. The difference in the common stock and conversion prices results in a beneficial conversion feature, a nondetachable conversion feature that is in the money at the commitment date. This resulting benefit is recorded as a convertible debt discount, with a corresponding increase to additional paid-in capital, and amortized using the effective interest method over the period from the commitment date (borrowing date) to the maturity date of the convertible debt.

Warranty ObligationsIncome (Expense):

We provide for the estimated cost of warranties at the time the related revenue is recognized based on the number of units sold, historical and anticipated rates of warranty claims, and cost per claim. We periodically assess the adequacy of our recorded warranty liabilities and adjust the amounts as necessary. Warranty  Other expense is recorded in cost of sales in our consolidated statement of operations.

Results of Operations (Dollars in thousands, except per share amounts)

Net Sales

In the medical segment, we track sales of our endoscopes and EndoSheath technology by market. We also track sales of peripherals and accessories that can be sold to more than one market. Net sales by operating segment and by market/category for the three and six months ended September 30, 2014 and 2013, respectively, were as follows:

  

Three Months Ended

      

Six Months Ended

     
  

September 30,

      

September 30,

     

Market/Category

 

2014

  

2013

  

Change

  

2014

  

2013

  

Change

 

Urology

 $1,928  $1,681   15% $3,701  $3,542   4%

ENT

  510   403   27%  761   743   2%

TNE

  76   355   -79%  257   558   -54%

Pulmonology

  227   395   -43%  592   481   23%

Repairs, peripherals, and accessories

  526   565   -7%  1,016   1,104   -8%

Total medical sales

  3,267   3,399   -4%  6,327   6,428   -2%

Total industrial sales

  843   569   48%  1,535   1,192   29%

Net sales

 $4,110  $3,968   4% $7,862  $7,620   3%

 Net sales increased $0.1 million, or 4%, to $4.1 millionwas $339,000 for the three months ended SeptemberJune 30, 20142015, compared with $4.0 million during the prior-year period. In our medical segment, increasesto other income of $4,000 in our sales to the urology and ENT markets were offset by decreases in sales to the TNE and pulmonology markets, resulting in a decrease of 4%, or $0.1 million, to $3.3 million, compared with $3.4 million during the prior-year period. Industrial segment sales increased 48% or $0.2 million, to $0.8 million, primarily due to the addition of new customers.

Net sales increased $0.2 million, or 3%, to $7.9 million for the six months ended September 30, 2014 compared with $7.6 million during the prior-year period. During the six months ended September 30, 2014, our medical segment’s net sales of $6.3 million decreased by $0.1 million, or 2%, as increased sales to the urology, pulmonology and ENT markets were offset by decreases in sales to the TNE market and a decline in repairs, peripherals and accessories. Our industrial segment’s net sales of $1.5 million increased by $0.3 million or 29%, primarily due to the addition of new customers.


The following table summarizes net sales by market/category and by product for our medical operating segment for the three and six months ended September 30, 2014 and 2013, respectively:

  

Three Months Ended

      

Six Months Ended

     
  

September 30,

      

September 30,

     

Market/Category

 

2014

  

2013

  

Change

  

2014

  

2013

  

Change

 

Urology

                        

Endoscopes

 $520  $975   -47% $1,262  $2,011   -37%

EndoSheath disposables

  1,408   706   99%  2,439   1,531   59%

Total urology market

  1,928   1,681   15%  3,701   3,542   4%

ENT

                        

Endoscopes

  510   403   27%  761   743   2%

TNE

                        

Endoscopes

  37   302   -88%  162   455   -64%

EndoSheath disposables

  39   53   -26%  95   103   -8%

Total TNE market

  76   355   -79%  257   558   -54%

Pulmonology

                        

Endoscopes

  160   358   -55%  470   388   21%

EndoSheath disposables

  67   37   81%  122   93   31%

Total pulmonology market

  227   395   -43%  592   481   23%

Repairs, peripherals, and accessories

  526   565   -7%  1,016   1,104   -8%

Total medical sales

 $3,267  $3,399   -4% $6,327  $6,428   -2%

Product

                        

Endoscopes

 $1,227  $2,038   -40% $2,655  $3,597   -26%

EndoSheath disposables

  1,514   796   90%  2,656   1,727   54%

Repairs, peripherals, and accessories

  526   565   -7%  1,016   1,104   -8%

Total medical sales

 $3,267  $3,399   -4% $6,327  $6,428   -2%

Net sales to the urology market of $1.9 million and $3.7 million for the three and six months ended September 30, 2014, respectively, increased by $0.2 million, or 15%, and by $0.2 million, or 4%, compared with their prior-year periods. Prior to May 2014, Stryker had the rights to market and sell our cystoscopes, the CST- 5000 Video Cystoscope and the CST-4000 Fiber Cystoscope, and the accompanying EndoSheath technology, peripherals and accessories. During May 2014, we began to market and sell the cystoscopes, their EndoSheaths, peripherals and accessories direct in the U.S. Lower sales of endoscopes have resulted from this changeover. However, this decrease has been more than offset by increased sales of Endosheath disposables.

Net sales to the ENT market of $0.5 million and $0.8 million for the three and six months ended September 30, 2014, respectively, increased by $0.1 million, or 27%, and $20 thousand or 2%, respectively, compared with their prior-year periods. In September 2014, we announced the introduction of a new ENT-7000 model that features the smallest diameter insertion tube available at 2.4mm in size.

Net sales to the TNE market of $0.1 million and $0.3 million for the three and six months ended September 30, 2014, respectively, decreased by $0.3 million, or 79%, and $0.3 million, or 54%, respectively compared with their prior-year periods. Our salesforce has been focused with the changes in the urology market discussed above, contributing to a decline in sales activity in this market.

Net sales to the pulmonology market of $0.2 million for the three months ended SeptemberJune 30, 2014 decreased by $0.2 million, or 43%, compared with the prior-year period. However, sales for the six months ended September 30, 2014 of $0.6 million increased by $0.1 million, or 23%, from the same period one year ago.2014.  The increase in other expense was primarily due to the launchrelated party debt assumed in the merger with Vision-Sciences.  The related party debt has a weighted average stated interest rate of a new video-based bronchoscope and digital processing unit, the BRS-5100.


Net sales1.07% resulting in $75,000 of all repairs, peripherals, and accessories forinterest expense in the quarter.  Further, as part of the purchase price accounting related to the merger, the related part debt was discounted to fair value.  For the three months ended SeptemberJune 30, 2014 of $0.5 million were within $39 thousand2015, the non-cash amortization of the prior-year period, while sales for the six months ended September 30, 2014 decreased by $0.1 million, or 8%, compared with the prior-year period.

debt discount totaled $266,000.


Income Tax Expense

Gross Profit (Net Sales Less Cost of Sales)

Gross profit by operating segment for the three and six months ended September 30, 2014 and 2013, respectively, was as follows:

  

Three Months Ended

      

Six Months Ended

     
  

September 30,

      

September 30,

     

Gross Profit

 

2014

  

2013

  

Change

  

2014

  

2013

  

Change

 

Medical

 $1,023  $981   4% $1,921  $1,774   8%

As percentage of net sales

  31.3%  28.9%      30.4%  27.6%    

Industrial

  235   214   10%  486   501   -3%

As percentage of net sales

  27.9%  37.6%      31.7%  42.0%    

Gross profit

 $1,258  $1,195   5% $2,407  $2,275   6%

Gross profit margin percentage

  30.6%  30.1%      30.6%  29.9%    

The gross profit margin percentage of 30.6% for the three and six months ended September 30, 2014 increased from 30.1% and 29.9% for the prior-year periods, respectively. The increase was due to an improved margin in the medical products segment, resulting from cost savings efforts as a result of our direct selling of cystoscopes, their EndoSheaths, peripherals and accessories direct in the U.S., somewhat offset by declines in the industrial products segment’s gross margins.

Operating Expenses(Selling, General, and Administrative (“SG&A”) and Research and Development (“R&D”)

Operating expenses by operating segment for the three andsix months ended September 30, 2014 and 2013, respectively were as follows:

  

Three Months Ended

      

Six Months Ended

     
  

September 30,

      

September 30,

     

Operating Expenses

 

2014

  

2013

  

Change

  

2014

  

2013

  

Change

 

SG&A expenses

                        

Medical

 $2,117  $1,898   12% $4,317  $4,659   -7%

Industrial

  241   152   59%  532   441   21%

Total SG&A expenses

  2,358   2,050   15%  4,849   5,100   -5%

R&D expenses

                        

Medical

  341   428   -20%  877   847   4%

Industrial

  -   -   -   -   -   - 

Total R&D expenses

  341   428   -20%  877   847   4%

Total operating expenses

 $2,699  $2,478   9% $5,726  $5,947   -4%

Selling, General, & Administrative (“SG&A”) Expenses

Selling, general and administrative (“SG&A”) expenses were $2.4 million for:  During the three months ended SeptemberJune 30, 2015 and 2014, an increasewe recorded income tax expense of $0.3 million, or 15%, compared with the prior-year period. The increase was primarily attributable$17,578 and $19,814, respectively. Income tax expense is attributed to our European subsidiaries and to the prior-year period which includedpayment of minimum taxes in the reversal of stock-basedU.S.


Non-GAAP Financial Measures:  The following table reconciles our operating loss calculated in accordance with GAAP to non-GAAP financial measures that exclude non-cash charges for share-based compensation expense, long-term incentive plan, depreciation and amortization and merger related costs.  The non-GAAP financial measures used by management and disclosed by us are not a substitute for, or superior to, financial measures and consolidated financial results calculated in accordance with GAAP, and you should carefully evaluate our reconciliations to non-GAAP.  We may calculate our non-GAAP financial measures differently from similarly titled measures used by other companies.  Therefore, our non-GAAP financial measures may not be comparable to those used by other companies.  We have described the reconciliations of each of our non-GAAP financial measures described above to the resignationmost directly comparable GAAP financial measures.

We use these non-GAAP financial measures, and in particular, non-GAAP operating loss, for internal managerial purposes because we believe such measures are one important indicator of the strength and the operating performance of our former chief executive officer. SG&A expenses were $4.8 millionbusiness.  Analysts and investors frequently ask us for this information.  We believe that they use these measures to evaluate the six months ended September 30, 2014,overall operating performance of companies in our industry, including as a decreasemeans of $0.3 million, or 5%, comparedcomparing period-to-period results and as a means of evaluating our results with the prior-year period, primarily attributable to our cost savings measures and that the prior-year period included severance expenses from our former chief executive officer.

those of other companies.

Research & Development (“R&D”)Expenses

Research

Our non-GAAP operating loss, excluding non-cash expenses and development (“R&D”) expenses were $0.3 million formerger related costs, during the three months ended SeptemberJune 30, 2015 and 2014 a decreasewas approximately $(1,694,000) and $(1,778,000), respectively.
    Expense Adjustments   
Three-Months Ended GAAP  
Share-
based
Expense
  
Long-term
Incentive
Plan
  Depreciation  Amortization  Non-GAAP 
June 30, 2015            
Gross profit $7,497,000  $10,000  $-  $52,000  $-  $7,559,000 
% of net sales  67.2%                  88.5%
Operating expenses                        
General and administrative  2,159,000   (124,000)  29,000   (58,000)  -   2,006,000 
Research and development  1,074,000   (17,000)  -   (8,000)  -   1,049,000 
Selling and marketing  6,842,000   (74,000)  -   (101,000)  -   6,667,000 
Amortization  634,000   -   -   -   (634,000)  - 
   10,709,000   (215,000)  29,000   (167,000)  (634,000)  9,722,000 
                         
Operating loss $(3,212,000) $225,000  $(29,000) $219,000  $634,000  $(2,163,000)
Merger Related  costs                      469,000 
Operating loss excluding merger related costs                     $(1,694,000)
                         
June 30, 2014                        
Gross profit $5,593,000  $13,000  $-  $5,000  $-  $5,611,000 
% of net sales  87.6%                  87.9%
Operating expenses                        
General and administrative  1,577,000   (212,000)  -   (39,000)  -   1,326,000 
Research and development  909,000   (18,000)  -   (1,000)  -   890,000 
Selling and marketing  5,273,000   (80,000)  -   (20,000)  -   5,173,000 
Amortization  8,000   -   -   -   (8,000)  - 
   7,767,000   (310,000)  -   (60,000)  (8,000)  7,389,000 
                         
Operating loss $(2,174,000) $323,000  $-  $65,000  $8,000  $(1,778,000)
Liquidity and the timingCapital Resources

Cash Flows.

On June 30, 2015, our cash and cash equivalents balances totaled $5,996,000 and we had working capital of expenses. approximately $9,343,000.

For the six months ended September 30, 2014, R&D expenses increased $30 thousand, or 4%, over the same period last year.

Other Expense

Other (expense) income for the three and six months ended September 30, 2014 and 2013, respectively, were as follows:

  

Three Months Ended

      

Six Months Ended

     
  

September 30,

      

September 30,

     

Other Expense

 

2014

  

2013

  

Change

  

2014

  

2013

  

Change

 

Interest expense

  (106)  (44)  141%  (189)  (85)  122%

Other, net

  4   7   -43%  (12)  3   -500%

Other expense

 $(102) $(37)  176% $(201) $(82)  145%

Other expense for the three and six months ended September 30, 2014 increased compared with their respective comparison periods due to interest expense resulting from a higher amount outstanding of convertible debt-related party and the amortization of debt discount.

Net Loss

Net loss of $(1.5) million for the three months ended SeptemberJune 30, 2014 increased from $(1.3) million2015, we used $2,895,000 of cash in the prior-year period. However, net lossoperating activities, compared to $1,505,000 of $(3.5) million for the six months ended September 30, 2014 improved from $(3.8) million in the prior-year period as a result of lower SG&A expenses and higher gross profit.

Net Lossper Common Share – Basic and Diluted

Net loss per basic and common share remained unchanged at $(0.03) per share forcash used during the three months ended SeptemberJune 30, 20142014.  We used this cash primarily to fund the operating loss, net of non-cash charges for depreciation, amortization of intangibles, long-term incentive plan and September 30, 2013, and remained unchanged at $(0.08) per share forshare-based compensation of $1,049,000 during the sixthree months ended SeptemberJune 30, 20142015, and September 30, 2013.

Liquidity, Capital Resources, and Outlook

The following table summarizes selected financial information as of September 30, 2014 and March 31, 2014:

  

September 30,

2014

  

March 31,

2014

 

Cash and cash equivalents

 $1,395  $1,237 

Accounts receivable, net

 $2,920  $3,818 

Inventories, net

 $4,221  $4,194 

Working capital

 $5,887  $6,863 

Our cash and cash equivalents and availability of $3.0 million on$396,000 during the 2014 Note are our principal sources of liquidity. Cash and cash equivalents at September 30, 2014 were $1.4 million compared with $1.2 million at March 31, 2014. Working capital was $5.9 million at September 30, 2014 compared with $6.9 million at March 31, 2014.

For the sixthree months ended SeptemberJune 30, 2014.


During the three months ended June 30, 2015 we used $(395,000) of net cash from the purchases of property, plant and equipment and during the three months ended June 30, 2014, we used $1.8 milliongenerated $3,000,000 of net cash in our operating activities, an improvementfrom the maturity of $1.4 million compared with $3.2 million in the prior-year period.

marketable securities.

As a result

Sources of better cash management, for the six months ended September 30, 2014 we issued $2.0 million in convertible debt-related party compared with $3.0 million in the prior-year period. On October 24, 2014, we drew down another $1.0 million under the 2014 Note.

OutlookLiquidity

.


We have incurred substantial operating losses since our inception and there can be no assurance that we will ever achieve or sustain a profitable level of operations in the future.inception. We anticipate that we will continue to incur negative cash flows from operations during fiscal 2015,2016, driven by continued investment in a direct sales force for the U.S. market, spending for marketing revitalizing aand for research and development, pipeline,integration of UPI and VSCI, and general business operations. As of SeptemberJune 30, 2014,2015, we had cash and cash equivalents totaling approximately $1.4$6.0 million. We expect that our cash at September 30, 2014, together with the $3.0 million of capital availableplan to us under the 2014 Note as of September 30, 2014, plus the $2.5 million of capital to be made available to us under the Existing Letter Agreement, should be sufficient to fund our operations through at least December 31, 2015. On October 24, 2014, we drew down another $1.0 million under the 2014 Note. However, if our performance expectations fall short (including our failure to generate expected levels of sales) or our expenses exceed expectations, or if the commitments under the 2014 Note or the Existing Letter Agreement become unavailable, we will need to secureobtain additional financingdebt and/or reduce our expenses to continue our operations. Our failure to do so would have a material adverse impact on our prospects and financial condition.equity financing during fiscal 2016.   There can be no assurance that any contemplated additional financing will be available on terms acceptable to us, if at all. If required, we believe we would be able to reduce our expenses to a sufficient level to continue to operate as a going concern.

Off-Balance Sheet Arrangements

At September 30, 2014, we had no off-balance sheet arrangements that have, or are reasonably likely


Our ability to have, a current or future effectachieve significant revenue growth will depend, in large part, on our financial condition, changesability to achieve widespread market acceptance of our products and successfully expand our business in financial condition, revenuesthe U.S.  We cannot guarantee that we will successfully achieve such revenue growth.  If we fail to meet our projections of profitability and cash flow, or expenses, results of operations, liquidity, capital expenditures, or capital resources.

determine to use cash for matters we are not currently projecting, we may need to seek additional financing to meet our cash needs.  We cannot assure you that such financing, if needed, will be available to us on acceptable terms, if at all.

Item

ITEM 3. Quantitative and Qualitative Disclosures About Market Risk

QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK


We are a smaller reporting company as defined in Rule 12b-2 of the Exchange Act, and are not required to provide the information required by this item.

Item.

ITEM 4. CONTROLS AND PROCEDURES

Item 4.Disclosure Controls and Procedures

Evaluation ofDisclosure Controls and Procedures

For the quarterly period ended September 30, 2014, we carried out an evaluation, under.


Under the supervision and with the participation of our management, including our President and Chief Executive Officer (“CEO”) and our PrincipalChief Financial Officer (“CEO and Principal Accounting Officer (“PFO”CFO”), ofwe evaluated the effectiveness of the design and operation of our disclosure controls and procedures pursuant to Rules(as defined in Rule 13a-15(e) and 15d-15(e)) under the Securities Exchange Act of 1934, as amended (the “Exchange Act”).  Based on this evaluation, our CEO and CFO concluded that, as of the end of the period covered by this report.

Our management, including our CEO and our PFO, does not expect that our disclosure controls and procedures will prevent all errors or fraud. A control system, no matter how well designed and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met andreport, our disclosure controls and procedures are designedeffective in ensuring that the information required to provide this reasonable assurance. Based uponbe disclosed by us in the evaluation discussed above,reports that we file or submit under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in applicable rules and forms and that such information is accumulated and communicated to our management, including our CEO and CFO, in a manner that allows timely decisions regarding required disclosure.


Changes In Internal Control Over Financial Reporting.

On March 31, 2015, the merger between Vision-Sciences and Uroplasty was completed.  As part of our PFO concluded that, as of September 30, 2014,ongoing activities after the merger, we are continuing to integrate our disclosurefinancial reporting functions and our controls and procedures were effective at providing such reasonable assurance.

Changesprocedures.  We have also been augmenting our company-wide controls to reflect the risks inherent in Internal Controls Over Financial Reporting

There have been no changes in our internal controls over financial reporting duringa business combination of the six months ended September 30, 2014 that have materially affected, or are reasonably likely to materially affect our internal controls over financial reporting.

magnitude and complexity of the merger.

PART II. OTHER INFORMATION
 


PART IIOTHER INFORMATION

Item

ITEM 1. Legal Proceedings

None

LEGAL PROCEEDINGS

Although we are not currently involved in any material legal proceedings, from time to time we may be subject to various pending or threatened legal actions and proceedings, including those that arise in the ordinary course of our business.  Such matters are subject to many uncertainties and to outcomes that are not predictable with assurance and that may not be known for extended periods of time.

Item

ITEM 1A. Risk Factors

There have been no material changes fromRISK FACTORS


We are affected by risks specific to us as well as factors that affect all businesses operating in a global market. For a discussion of the information discussed in Part I, Item 1A. Risk Factors beginning on page 14 ofspecific risks that could materially adversely affect our Annual Reportbusiness, financial condition or operating results, please see our annual report on Form 10-K for the fiscal year ended March 31, 2014,except for the information discussed below. You should carefully consider the risks and uncertainties we discussed in our Form 10-K and the risks described below in this quarterly report before deciding to invest in, or retain, shares of our common stock. These are not the only risks and uncertainties that we face. Additional risks and uncertainties that we do not currently know about or that we currently believe are immaterial, or that we have not predicted, may also harm our business operations or adversely affect us. If any of these risks or uncertainties actually occurs, our business, financial condition, operating results, or liquidity could be materially harmed.

We have a history of operating losses and we may not achieve or maintain profitability in the future

We have incurred substantial operating losses since our inception and there can be no assurance that we will ever achieve or sustain a profitable level of operations in the future. We anticipate negative cash flows from operations during the remainder of fiscal 2015 driven by continued investment in a direct sales force for the U.S. market, spending for marketing, spending for research and development and general business operations. As of September 30, 2014, we had cash and cash equivalents totaling approximately $1.4 million. We expect that our cash at September 30, 2014, together with up to $3.0 million of capital available to us under the 2014 Note at September 30. 2014, plusheading “Part I — Item 1A. Risk Factors.” There has been no material change from the $2.5 million of capital to be made available to us under the Existing Letter Agreement, subject to certain conditions and an expiration date of January 1, 2016 (seeNote 1. Summary of Significant Accounting Policies and Note 5. Convertible Debt – Related Party for additional information), should be sufficient to fund our operations through at least December 31, 2015. On October 24, 2014 we drew down another $1.0 million under the 2014 Note. However, if our performance expectations fall short (including our failure to generate expected levels of sales) or our expenses exceed expectations, or if the commitments under the 2014 Note or the Existing Letter Agreement become unavailable, we will need to secure additional financing and/or reduce our expenses to continue our operations. Our failure to do so would have a material adverse impact on our prospects and financial condition. There can be no assurancerisk factors as disclosed in that any contemplated additional financing will be available on terms acceptable to us, if at all. If required, we believe we would be able to reduce our expenses to a sufficient level to continue to operate as a going concern.

Our officers and directors have the ability to exercise significant control over the Company

As of September 30, 2014, our officers and directors owned an aggregate of approximately 37% of our outstanding common stock. Under the Replacement Note, Mr. Pell, at his option, has the right to convert the unpaid principal balance thereof, which was $20.0 million as of September 30, 2014, into 16,666,666 shares of our common stock. Under the 2013 Note, Mr. Pell, at his option, has the right to convert the unpaid principal balance thereof, which was $3.5 million as of September 30, 2014, into 3,932,584 shares of our common stock. Under the 2014 Note, Mr. Pell, at his option, has the right to convert the unpaid principal balance thereof, which was $2.0 million as of September 30, 2014, into 1,801,801 shares of our common stock. The conversion of the Replacement Note, the 2013 Note and the 2014 Note, or the Notes, would increase the aggregate ownership of our officers and directors to approximately 57% of our common stock. As such, upon conversion of the Notes, our directors and officers exercise significant control over all matters requiring stockholder approval, including the election of directors and approval of significant corporate transactions. This concentration of ownership may have the effect of delaying or preventing a change in control of the Company or forcing management to change its operating strategies, which may be to the benefit of management but not in the interest of the stockholders

annual report

Item

ITEM 2. Unregistered SalesUNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS

Information regarding the Company’s stock repurchases during the three months ended June 30, 2015 is as follows:

Period 
Total
Number of
Shares
Purchased(a)
  
Average Price
Paid per Share
  
Total Number of Shares
Purchased as Part of
Publicly Announced Plans
or Programs
  
Maximum Number of
Shares that May Yet
Be Purchased Under
the Plans or Programs
 
April 1, 2015 - April 30, 2015  1,886  $1.66   -   - 
May 1, 2015 - May 31, 2015  -   -   -   - 
June 1, 2015 - June 30, 2015  744   1.68   -   - 
Total  2,630  $1.67   -   - 
(a)Represent shares surrendered to cover tax obligation for restricted stock vested.

Item

ITEM 3. Defaults Upon Senior Securities

None

DEFAULTS UPON SENIOR SECURITIES

None.

Item

ITEM 4.Mine Safety Disclosures

None

MINE SAFETY DISCLOSURE

Not applicable.

Item

ITEM 5. Other Information

None

OTHER INFORMATION

None.

Item

ITEM 6. EXHIBITS

Exhibits


Exhibits

Exhibit
No.
ExhibitMethod of Filing
*2.1Agreement and Plan of Merger dated as of December 21, 2014 by and among Vision-Sciences, Inc., Visor Merger Sub LLC, and Uroplasty, Inc.Incorporated by reference to Exhibit 2.1 to Current Report on Form 8-K as filed with the SEC on December 22, 2014 (File No. 000-20970)
  

10.1

3.1
 

Letter Agreement dated October 28, 2014 between the Company(a) Amended and Lewis C. Pell.

31.1

Restated Certificate of Incorporation.
 

CertificationsIncorporated by reference to Exhibit 3.1 to Annual Report on Form 10-K for the fiscal year ended March 31, 2001 (File No. 000-20970)

(b) Certificate of Chief Executive OfficerAmendment to Certificate of Incorporation.Incorporated by reference to Exhibit 3.1 to Annual Report on Form 10-K for the fiscal year ended March 31, 2001 (File No. 000-20970)
(c) Certificate of Amendment to Certificate of Incorporation.Incorporated by reference to Exhibit 99.2 to Current Report on Form 8-K as filed with the SEC on December 15, 2010 (File No. 000-20970)
(d) Certificate of Amendment to Certificate of Incorporation.Incorporated by reference to Exhibit 99.1 to Current Report on Form 8-K as filed with the SEC on August 1, 2014 (File No. 000-20970)
(e) Certificate of Amendment to Amended and Restated Certificate of Incorporation.Incorporated by reference to Exhibit 3.1 to Current Report on Form 8-K as filed with the SEC on March 31, 2015 (File No. 000-20970)
(f) Certificate of Amendment to Amended and Restated Certificate of Incorporation.Incorporated by reference to Exhibit 3.2 to Current Report on Form 8-K as filed with the SEC on March 31, 2015 (File No. 000-20970)
3.2Amended and Restated Bylaws.Incorporated by reference to Exhibit 99.2 to Current Report on Form 8-K as filed with the SEC on July15, 2009 (File No. 000-20970)
Description of Non-Employee Director CompensationFiled herewith
Certification by the CEO pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

31.2

 

Certifications of Principal Financial Officer and Principal Accounting OfficerFiled herewith

Certification by the CFO pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

32

 

Certifications of Chief Executive Officer and Principal Financial Officer and Principal Accounting OfficerFiled herewith

Certification by the CEO pursuant to Section 18 USC Section 1350, as adopted pursuant to Section 906 of the Sarbanes OxleySarbanes-Oxley Act of 2002

Filed herewith
   

101.INS**

 

XBRL Instance

101.SCH**

Certification by the CFO pursuant to Section 18 USC Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
 

XBRL Taxonomy Extension Schema

Filed herewith

101.CAL**

101.INS
 

XBRL Taxonomy Extension Calculation

101.DEF**

Instance
 

XBRL Taxonomy Extension Definition

101.LAB**

XBRL Taxonomy Extension Labels

101.1PRE**

XBRL Taxonomy Extension Presentation

Furnished herewith **
   
* Filed herewith.
**101.SCH XBRL information is furnished and not filed or a part of a registration statement or prospectus for purposes of sections 11 or 12 of the Securities Act of 1933, as amended, is deemed not filed for purposes of section 18 of the Securities Exchange Act of 1934, as amended, and otherwise is not subject to liability under these sections.Taxonomy Extension SchemaFurnished herewith **
101.CALXBRL Taxonomy Extension CalculationFurnished herewith **
101.DEFXBRL Taxonomy Extension DefinitionFurnished herewith **
101.LABXBRL Taxonomy Extension LabelsFurnished herewith **
101.PREXBRL Taxonomy Extension PresentationFurnished herewith **

 

* Certain schedules to the Agreement and Plan of Merger have been omitted pursuant to Item 601(b)(2) of Regulation S-K.  We will furnish copies of any such omitted schedules to the SEC upon request.

** XBRL information is furnished and not filed or a part of a registration statement or prospectus for purposes of sections 11 or 12 of the Securities Act of 1933, as amended, is deemed not filed for purposes of section 18 of the Securities Exchange Act of 1934, as amended, and otherwise is not subject to liability under these sections.


SIGNATURES

Pursuant to


In accordance with the requirements of the Securities Exchange Act of 1934, the Registrant has dulyregistrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.


 

VISION-SCIENCES,

COGENTIX MEDICAL, INC.

 
Date: November 13, 2014August 14, 2015
By: /s/ Howard ZaubermanROBERT KILL
Robert Kill
President, Chief Executive Officer and Chairman of the
Board
 

Howard Zauberman
President and Chief Executive Officer

Date: August 14, 2015
 
Date: November 13, 2014
By: /s/ Gary Siegel

Gary Siegel
BRETT REYNOLDS

Brett Reynolds
Senior Vice President, Finance,

PrincipalChief Financial Officer and
Principal
Accounting Officer

Corporate Secretary

28

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