UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 
Form 10-Q
   
þ Quarterly Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
For the quarterly period endedMarch 31,September 30, 2006
   
o Transition Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
For the transition period from                    to                    
Commission File Number:0-4136
Lifecore Biomedical, Inc.
(Exact name of registrant as specified in its charter)
   
Minnesota 41-0948334
   
(State or other jurisdiction of (IRS Employer Identification No.)
incorporation or organization)  
   
3515 Lyman Boulevard  
Chaska, Minnesota 55318
   
(Address of principal executive (Zip Code)
offices)  
Registrant’s telephone number, including area code:952-368-4300
Not Applicable
(Former name, former address and former fiscal year,
if changed since last report.)
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports) and (2) has been subject to such filing requirements for the past 90 days.
Yesþ    Noo
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, or a non-accelerated filer. See definition of “accelerated filer and large accelerated filer” in Rule 12b-2 of the Exchange Act. (Check one):
Large accelerated filero     Accelerated filerþ     Non-accelerated filero
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).
Yeso    Noþ
The number of shares outstanding of the registrant’s Common Stock, $.01 par value, as of May 1,November 3, 2006 was 13,190,54613,256,153 shares.
 
 

 


 

LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
FORM 10-Q
TABLE OF CONTENTS
       
    Page
 Financial Information    
       
 Item 1. Financial Statements — Unaudited    
       
  Condensed Consolidated Balance Sheets at March 31,September 30, 2006 and June 30, 20052006  2 
       
  Condensed Consolidated Statements of Operations for Three Months and Nine Months Ended March 31,September 30, 2006 and 2005  3 
       
  Condensed Consolidated Statements of Cash Flows for NineThree Months Ended March 31,September 30, 2006 and 2005  4 
       
  Notes to Condensed Consolidated Financial Statements  5-125-10 
       
 Management’s Discussion and Analysis of Financial Condition and Results of Operations  13-2111-17 
       
 Quantitative and Qualitative Disclosures About Market Risk  2218 
       
 Controls and Procedures  2218 
       
 Other Information    
       
 Legal Proceedings  2319 
       
 Exhibits  2420 
       
  2521 
       
Exhibit Index  2622 
Stock Option Plan
 Certification of CEO Pursuant to Section 302
 Certification of CFO Pursuant to Section 302
 Certification of CEO Pursuant to Section 906
 Certification of CFO Pursuant to Section 906

1


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS
CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited)
                
 March 31, June 30,  September 30, June 30, 
 2006 2005  2006 2006 
ASSETS  
Current Assets  
Cash and cash equivalents $22,134,000 $18,508,000  $28,110,000 $26,638,000 
Accounts receivable, less allowances 11,767,000 10,171,000  12,065,000 12,564,000 
Inventories 12,048,000 9,456,000  12,912,000 12,217,000 
Deferred income taxes, net 5,183,000 4,190,000  5,640,000 4,865,000 
Prepaid expenses 1,032,000 780,000  1,154,000 1,084,000 
          
Total current assets 52,164,000 43,105,000  59,881,000 57,368,000 
  
Property, plant and equipment  
Land, building and equipment 48,719,000 47,400,000  49,680,000 49,388,000 
Less accumulated depreciation  (25,601,000)  (24,211,000)  (26,643,000)  (26,138,000)
          
 23,118,000 23,189,000  23,037,000 23,250,000 
  
Other Assets  
Intangibles, net 5,247,000 4,799,000  5,173,000 5,201,000 
Inventories 1,977,000 2,409,000  1,315,000 1,406,000 
Deferred income taxes, net 2,558,000 6,062,000  354,000 1,694,000 
Other 368,000 302,000  308,000 319,000 
          
 10,150,000 13,572,000  7,150,000 8,620,000 
          
 $85,432,000 $79,866,000  $90,068,000 $89,238,000 
          
  
LIABILITIES AND SHAREHOLDERS’ EQUITY  
Current Liabilities  
Current maturities of long-term obligations $285,000 $285,000  $290,000 $290,000 
Accounts payable 3,020,000 3,418,000  2,835,000 3,212,000 
Accrued compensation 1,442,000 1,920,000  1,283,000 1,847,000 
Accrued expenses 1,371,000 1,293,000  1,602,000 1,549,000 
          
Total current liabilities 6,118,000 6,916,000  6,010,000 6,898,000 
  
Long-term obligations 4,902,000 5,089,000  4,734,000 4,804,000 
  
Shareholders’ equity 74,412,000 67,861,000  79,324,000 77,536,000 
          
 $85,432,000 $79,866,000  $90,068,000 $89,238,000 
          
See accompanying notes to condensed consolidated financial statements.

2


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)
                        
 Three months ended March 31, Nine months ended March 31,  Three months ended September 30, 
 2006 2005 2006 2005  2006 2005 
Net sales $16,775,000 $14,247,000 $45,409,000 $40,770,000  $15,010,000 $13,425,000 
Cost of goods sold 6,208,000 5,587,000 17,399,000 16,138,000  5,572,000 5,074,000 
              
Gross profit 10,567,000 8,660,000 28,010,000 24,632,000  9,438,000 8,351,000 
  
Operating expenses  
Research and development 881,000 1,235,000 2,878,000 3,254,000  1,096,000 1,014,000 
Marketing and sales 4,525,000 3,661,000 12,661,000 10,713,000  4,912,000 4,064,000 
General and administrative 1,720,000 1,660,000 5,275,000 4,706,000  1,924,000 1,706,000 
              
 7,126,000 6,556,000 20,814,000 18,673,000  7,932,000 6,784,000 
              
  
Operating income 3,441,000 2,104,000 7,196,000 5,959,000  1,506,000 1,567,000 
  
Other income (expense)  
Interest income 203,000 67,000 495,000 109,000  331,000 135,000 
Interest expense  (65,000)  (53,000)  (181,000)  (221,000)  (64,000)  (56,000)
Bond retirement expense     (290,000)
Currency transaction gains (losses)  122,000  (73,000) 320,000  73,000  (24,000)
Other 5,000  (3,000)  (14,000) 249,000  6,000  (14,000)
              
 143,000 133,000 227,000 167,000  346,000 41,000 
              
  
Income before income tax expense 3,584,000 2,237,000 7,423,000 6,126,000  1,852,000 1,608,000 
  
Income tax expense 1,391,000 129,000 2,794,000 359,000  713,000 563,000 
              
  
Net income $2,193,000 $2,108,000 $4,629,000 $5,767,000  $1,139,000 $1,045,000 
              
  
Net income per share  
Basic $0.17 $0.16 $0.35 $0.45  $0.09 $0.08 
              
Diluted $0.16 $0.15 $0.34 $0.43  $0.08 $0.08 
              
  
Weighted average shares outstanding  
Basic 13,180,859 12,993,379 13,134,280 12,957,033  13,223,448 13,059,567 
              
Diluted 13,572,205 13,670,465 13,505,079 13,279,991  13,672,260 13,460,056 
              
See accompanying notes to condensed consolidated financial statements.

3


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited)
                
 Nine months ended March 31,  Three months ended September 30, 
 2006 2005  2006 2005 
Cash flows from operating activities:  
Net income $4,629,000 $5,767,000  $1,139,000 $1,045,000 
Adjustments to reconcile net income to net cash provided by operating activities:  
Depreciation and amortization 1,470,000 1,523,000  535,000 473,000 
Allowance for doubtful accounts 106,000 333,000  48,000 10,000 
Deferred income taxes 2,511,000   565,000 485,000 
Stock compensation 786,000 106,000 
Tax benefit related to stock-based compensation plans 56,000  
Stock-based compensation 385,000 230,000 
Accumulated currency translation adjustment 90,000 65,000  70,000 28,000 
Changes in operating assets and liabilities, net of effects of acquisition:  
Accounts receivable  (1,986,000)  (1,204,000) 451,000 140,000 
Inventories  (2,058,000) 716,000   (604,000)  (1,533,000)
Prepaid expenses  (251,000)  (182,000)  (70,000)  (245,000)
Accounts payable  (409,000)  (526,000)  (377,000) 13,000 
Accrued liabilities  (413,000)  (81,000)  (511,000)  (474,000)
          
Net cash provided by operating activities 4,531,000 6,517,000  1,631,000 172,000 
  
Cash flows from investing activities:  
Purchases of property, plant and equipment  (1,287,000)  (1,113,000)  (292,000)  (445,000)
Acquisition, net of cash acquired  (346,000)     (322,000)
Refunds of security deposits  830,000 
Increase in other assets  (75,000)  (121,000)
Change in other assets 8,000  (45,000)
          
Net cash used in investing activities  (1,708,000)  (404,000)  (284,000)  (812,000)
  
Cash flows from financing activities:  
Payments on long-term obligations  (187,000)  (187,000)  (70,000)  (70,000)
Issuance of industrial revenue bonds  5,630,000 
Retirement of industrial revenue bonds   (5,986,000)
Proceeds from stock options exercised 990,000 656,000  195,000 706,000 
          
Net cash provided by financing activities 803,000 113,000  125,000 636,000 
          
Net increase in cash and cash equivalents 3,626,000 6,226,000 
Net increase (decrease) in cash and cash equivalents 1,472,000  (4,000)
Cash and cash equivalents at beginning of period 18,508,000 8,553,000  26,638,000 18,508,000 
          
Cash and cash equivalents at end of period $22,134,000 $14,779,000  $28,110,000 $18,504,000 
          
  
Supplemental disclosure of cash flow information:  
Cash paid during the period for:  
Interest $166,000 $271,000  $64,000 $56,000 
Taxes 253,000 347,000  141,000 21,000 
See accompanying notes to condensed consolidated financial statements.

4


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED STATEMENTS — UNAUDITED
(March 31, 2006)September 30, 2006
NOTE A – FINANCIAL INFORMATION
Lifecore Biomedical, Inc. (referred to in this report as “Lifecore” or the “Company”) manufactures biomaterials and surgical devices for use in various surgical markets and provides specialized contract aseptic manufacturing services through its two divisions, the Hyaluronan Division and the Oral RestorativeDental Division. The Company’s manufacturing facility is located in Chaska, Minnesota. The Hyaluronan Division markets its products through original equipment manufacturers and contract manufacturing alliances in ophthalmologic, orthopedic surgery, veterinary medicine and gynecologic fields. The Oral RestorativeDental Division markets its products through direct sales in the United States, Italy, Germany, Sweden and France and through distributors in other foreign countries.
The accompanying unaudited condensed consolidated financial statements have been prepared in accordance with Regulation S-X pursuant to the rules and regulations of the Securities and Exchange Commission. Certain information and footnote disclosures normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States have been condensed or omitted pursuant to such rules and regulations, although management believes that the disclosures are adequate to make the information presented not misleading.
In the opinion of management, the unaudited condensed consolidated financial statements contain all adjustments (consisting of only normal recurring adjustments) necessary to present fairly the financial position of the Company as of March 31,September 30, 2006, the results of operations for the three month and nine month periods ended March 31,September 30, 2006 and 2005, and cash flows for the ninethree month periods ended March 31,September 30, 2006 and 2005. The results of operations and cash flows for the ninethree months ended March 31,September 30, 2006 are not necessarily indicative of the results for the full year or of the results for any future periods. The unaudited condensed consolidated balance sheet as of June 30, 20052006 has been derived from audited financial statements as of that date.
In preparation of the Company’s consolidated financial statements, management is required to make estimates and assumptions that affect reported amounts of assets and liabilities and related revenues and expenses during the reporting periods. Actual results could differ from the estimates used by management.
NOTE B – INVENTORIES
Inventories are stated at the lower of cost (first-in, first-out method) or market. Inventories consist mainly of finished hyaluronan powder, aseptic units and oral restorativedental products and related raw materials. The Company’s inventory has been reduced to lower of cost or market for obsolete, excess or unmarketable inventory. The lower of cost or market adjustment is based on management’s review of inventories on hand compared to estimated future usage and sales. The portion of finished hyaluronan powder inventory not expected to be consumed within the next 12 months is classified as a long-term asset. The finished hyaluronan inventory is maintained in a frozen state and has a shelf life of ten years. Inventories consist of the following:
                
 March 31, June 30,  September 30, June 30, 
 2006 2005  2006 2006 
Raw Materials $4,540,000 $3,102,000  $4,340,000 $3,973,000 
Work-in-process 908,000 426,000  920,000 708,000 
Finished goods-current 6,600,000 5,928,000  7,652,000 7,536,000 
          
 12,048,000 9,456,000  12,912,000 12,217,000 
Finished goods-long term 1,977,000 2,409,000  1,315,000 1,406,000 
          
 $14,025,000 $11,865,000  $14,227,000 $13,623,000 
          

5


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS — UNAUDITED (continued)
March 31,September 30, 2006
NOTE C – INTANGIBLE ASSETS
Intangibles consist primarily of the cost of goodwill related to acquisitions, patents and distribution rights and licenses. All intangibles relate to the Oral RestorativeDental Division.
Also included within intangibles are costs incurred to register patents and trademarks, which are capitalized as incurred. Amortization of these costs commences when the related patent or trademark is granted. The costs are amortized over the estimated useful life of the patent or trademark, not to exceed 17 years.trademark.
Goodwill is tested for impairment on an annual basis, or when there is an indication that an impairment has occurred, and is written down when impaired by applying a fair value based test. Purchased intangible assets other than goodwill are amortized over their useful lives unless these lives are determined to be indefinite. There was no impairment recorded for the ninethree month period ended March 31,September 30, 2006.
     Intangibles consisted of the following at:
                
 March 31, June 30,  September 30, June 30, 
 2006 2005  2006 2006 
Goodwill $4,870,000 $4,352,000  $4,783,000 $4,783,000 
Patents 387,000 387,000  387,000 387,000 
Distribution rights and licenses 350,000 350,000  350,000 350,000 
Customer List 80,000 80,000 
Accumulated amortization  (360,000)  (290,000)  (427,000)  (399,000)
          
 $5,247,000 $4,799,000  $5,173,000 $5,201,000 
          
NOTE D – LINE OF CREDIT
The Company has a $5,000,000 credit facility with a bank which has a maturity date of December 31, 2006. The agreement allows for advances against eligible accounts receivable, subject to compliance with covenants. Under the credit facility, interest will accrue at the prime rate minus .5% or LIBOR plus 2.25%, at the Company’s option. At March 31,September 30, 2006 and June 30, 2005,2006, there were no balances outstanding under the line of credit.
NOTE E – STOCK-BASED COMPENSATION
Commencing July 1, 2005, the Company adopted Statement of Financial Accounting Standard No. 123R, “Share-Based Payment” (“SFAS 123R”), which requires all share-based payments, including grants of stock options, to be recognized in the income statement as an operating expense, based on their fair values over the requisite service period. The Company recorded $262,000$313,000 and $633,000$190,000 of related compensation expense for the three month and nine month periods ended March 31,September 30, 2006 and 2005, respectively.

6


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS — UNAUDITED (continued)
March 31,September 30, 2006
NOTE E – STOCK-BASED COMPENSATION – (continued)
The Company recognized stock-based compensation expense related to employee and non-employee options as follows:
                
 Three months ended Nine months ended  Three months ended September 30, 
 March 31, 2006 March 31, 2006  2006 2005 
Cost of goods sold $11,000 $32,000  $17,000 $11,000 
Research and development 14,000 43,000  65,000 14,000 
Marketing and sales 125,000 231,000  118,000 55,000 
General and administrative 112,000 327,000  113,000 110,000 
          
Total stock-based compensation expense $262,000 $633,000  $313,000 $190,000 
          
  
Effect on earnings per share, net of tax effects:  
Basic $0.02 $0.04  $0.02 $0.01 
          
Diluted $0.02 $0.04  $0.02 $0.01 
          
The Company reclassified stock-based compensation expense for the six monthsthree month period ended December 31,September 30, 2005. The Company classifies stock option expense based on option holders’ salary expense classification.
As of March 31, 2006, $1,428,000 of unrecognized compensation costs related to non-vested awards is expected to be recognized over a weighted average period of approximately 3.4 years.
Prior to adopting SFAS 123R, the Company accounted for stock-based compensation under Accounting Principles Board Opinion No. 25, “Accounting for Stock Issued to Employees.” The Company has applied the modified prospective method in adopting SFAS 123R. Accordingly, periods prior to adoption have not been restated. The following table illustrates the effect on net income and earnings per share if the fair value based method had been applied to the comparable periods in the prior fiscal year.
         
  Three months ended  Nine months ended 
  March 31, 2005  March 31, 2005 
Reported net income $2,108,000  $5,767,000 
Stock-based compensation determined under the fair value based method, net of related tax effects  (432,000)  (847,000)
       
Pro forma net income $1,676,000  $4,920,000 
       
         
Income per common equivalent share:        
Basic –as reported $0.16  $0.45 
Diluted – as reported $0.15  $0.43 
         
Basic – pro forma $0.13  $0.38 
Diluted – pro forma $0.12  $0.37 

7


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS — UNAUDITED (continued)
March 31, 2006
NOTE E – STOCK-BASED COMPENSATION – (continued)
The Company uses the Black-Scholes option pricing model to determine the weighted average fair value of options. The weighted average fair value of options granted duringDuring the three month periods ended March 31, 2006 and 2005 were $7.04 and $7.40, respectively, and were $6.68 and $4.83 during the nine month periods ended March 31, 2006 and 2005, respectively. The assumptions utilized to determine the fair value of options at the date of grant are indicated in the following table:
                         
  Three Months Ended Three Months Ended Three Months Ended
  March 31, December 31, September 30,
  2006 2005 2005 2004 2005 2004
Risk-free interest rate  4.85%  3.9%  4.33%  3.9%  4.27%  3.9%
Expected volatility  58.2%  69.6%  60.8%  69.6%  69.5%  69.6%
Expected life (in years)  5.7   5.4   5.7   5.4   5.6   5.4 
Dividend yield                  
The expected term of the options is based on evaluations of historical and expected future employee exercise behavior. The risk-free interest rate is based on the US Treasury rates at the date of grant with maturity dates approximately equal to the expected life at the grant date. Volatility is based on historical volatility of the Company’s stock. The Company has not historically issued any dividends and does not expect to in the foreseeable future.
The Company’s stock options generally vest ratably over four years of service and have a contractual life of 10 years. The Company has authorized 5,000,000 shares for grant under the 1990, 1996 and 2003 Stock Option Plans. Option transactions under the 1990 and 1996 Stock Option Plans during the nine month period ended March 31,September 30, 2006, are summarized as follows (no stock options have been granted under the 2003 Plan):
         
  Number of  Weighted Average 
  Shares  Exercise Price 
Outstanding at June 30, 2005  1,720,706  $10.19 
Granted  41,300   10.86 
Exercised  (101,100)  7.00 
Canceled  (12,750)  9.35 
       
Outstanding at September 30, 2005  1,648,156   10.41 
Granted  56,000   14.06 
Exercised  (18,233)  9.71 
Canceled  (11,400)  8.28 
       
Outstanding at December 31, 2005  1,674,523   10.52 
Granted  84,500   15.02 
Exercised  (13,375)  7.89 
Canceled  (49,250)  14.10 
       
Outstanding at March 31, 2006  1,696,398  $10.66 
       
         
  Number of  Weighted Average 
  Shares  Exercise Price 
Options exercisable at March 31, 2006  1,362,473  $10.68 

8


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS — UNAUDITED (continued)
March 31, 2006
NOTE E – STOCK-BASED COMPENSATION – (continued)
The following tables summarize information concerning currently outstanding and exercisable stock options.
            
Options Outstanding
 
Range of Number  Weighted Average Remaining  Weighted Average
Exercise Price Outstanding  Contractual Life  Exercise Price
$3.55  —    5.82  75,750  6.24 years  $5.20
5.83    —    8.75  688,730  6.25 years   7.29
8.76    —  13.12  409,875  6.45 years   10.22
13.13  —  19.68  491,043  3.70 years   15.91
19.69  —  23.38  31,000  1.76 years   21.55
          
   1,696,398      $10.66
          
         
  Options Exercisable  
 
Range of Number Weighted Average
Exercise Price Exercisable Exercise Price
$3.55  —    5.82  54,000 $  5.32
5.83    —    8.75  611,605  7.28
8.76    —  13.12  257,200  10.06
13.13  —  19.68  413,668  16.11
19.69  —  23.38  26,000  21.58
      
   1,362,473 $10.68
      
Restricted Stock Awards
During fiscal 2005, the Company granted 60,000 restricted common stock awards to its officers; 50,000 of the shares were awarded at a price of $9.30 and 6,667 of those shares were forfeited during the year ended June 30, 2005, and 10,000 of the shares were awarded at a price of $10.79. During the current quarter, the Company granted 7,0003,500 restricted common stock awards to a new officer at a price of $15.42. The restricted shares awarded in fiscal 2005 will vest at the earlier of four years from the date of issuance or upon achievement of financial performance criteria for fiscal years 2005, 2006 and 2007. The restricted shares awarded in fiscal 2006 will vest at the earlier of three years from the date of issuance or upon achievement of financial performance criteria for fiscal years 2006 and 2007. The Company achieved the financial performance criteria in fiscal 2005, and as a result, 20,000 shares vested. The employee forfeits unvested shares upon the termination of employment prior to the end of the vesting period.$15.91. Stock compensation expense recognized related to these grantsrestricted stock awards totaled $73,000$72,000 and $85,000$40,000 during the three month periods ended March 31, 2006 and 2005, respectively, and $153,000 and $106,000 during the nine month periods ended March 31,September 30, 2006 and 2005, respectively.
NOTE F – ACCUMULATED OTHER COMPREHENSIVE INCOME
The Company has $566,000$382,000 of accumulated currency translation adjustment which reduces shareholders’ equity at March 31,September 30, 2006. Total comprehensive income was $2,246,000$1,209,000 and $1,930,000$1,073,000 for the three month periods ended March 31,September 30, 2006 and 2005, respectively, and total comprehensive income was $4,719,000 and $5,832,000 for the nine month periods ended March 31, 2006 and 2005, respectively.

9


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS — UNAUDITED (continued)
March 31, 2006
NOTE G – NET INCOME PER SHARE
The Company’s basic net income per share amounts have been computed by dividing net income by the weighted average number of outstanding common shares. The Company’s diluted net income per share is computed by dividing net income by the weighted average number of outstanding common shares and common share equivalents relating to stock options and restricted stock, when dilutive. For the three and nine month periods ended March 31,September 30, 2006 391,346 and 370,799 common share equivalents, respectively, were included in the computation of diluted net income per share. For the three2005, 448,812 and nine month periods ended March 31, 2005, 677,086 and 322,958400,489 common share equivalents, respectively, were included in the computation of diluted net income per share.
Options to purchase 517,043377,668 shares of common stock with a weighted average exercise price of $16.27$17.18 for the three month and nine month periodsperiod ended March 31,September 30, 2006 and options to purchase 319,043 and 587,543465,543 shares of common stock with a weighted average exercise price of $17.53 and $15.20$16.39 for the three month and nine month periodsperiod ended March 31,September 30, 2005 respectively, were outstanding but were not included in the calculation of diluted net income per share because the options’ exercise prices were greater than the average market price of the Company’s common stock during those periods. Although these options were antidilutive for the periods presented, they may be dilutive in future period calculations.

7


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS — UNAUDITED (continued)
September 30, 2006
NOTE H – INCOME TAXES
Provision for income taxes was $1,391,000$713,000 at an effective rate of 38.5% and $129,000$563,000 at an effective rate of 35% for the three month periods ended March 31, 2006 and 2005, respectively, and the provision for income taxes was $2,794,000 and $359,000 for the nine month periods ended March 31,September 30, 2006 and 2005, respectively. The effective rate for the prior year period was significantly lower than the comparable periods in fiscal 2006 due to recognizing a tax benefit for the partial release in the deferred tax asset valuation allowance for the net operating losses utilized in the prior year period. As a result, the Company’s statement of earnings reflects more normal tax charges throughout fiscal 2006 and beyond. However, withWith the exception of the Alternative Minimum Tax and certain state taxes, the Company will not use cash for domestic income taxes until its net operating losses are fully realized on its tax returns.
NOTE I – SEGMENT INFORMATION
The Company operates in two business segments. The Hyaluronan Division manufactures, markets and sells products containing hyaluronan and provides contract aseptic packaging services. The Oral RestorativeDental Division produces and markets various oral restorativedental products to the area of implant dentistry. Currently, products containing hyaluronan are sold primarily to customers pursuant to ongoing supply agreements. The Company’s Oral RestorativeDental Division markets products directly to clinicians and dental laboratories in the United States, Germany, Italy, Sweden and France and primarily through distributorship arrangements in other foreign locations.
Segment assets and the basis of segmentation are consistent with that reported at June 30, 2006. Segment information for sales and income from operations are as follows:
         
  Three months ended September 30, 
  2006  2005 
Net sales        
Hyaluronan products $4,779,000  $4,661,000 
Dental products  10,231,000   8,764,000 
       
  $15,010,000  $13,425,000 
       
Income from operations        
Hyaluronan products $996,000  $1,138,000 
Dental products  510,000   429,000 
       
  $1,506,000  $1,567,000 
       
NOTE J — ACQUISITION OF BARDO-BIOTECH SAS
On August 12, 2005, the Company acquired 100% of the stock of Bardo-Biotech SAS, a privately-owned distributor of the Company’s Dental products located in Beauzelle, France. The Company included the operating results of Bardo-Biotech SAS in the financial statements from August 1, 2005, the effective date.
In conjunction with this acquisition, the consideration paid was $401,000 in cash and $362,000 in debt forgiveness. The acquisition resulted in goodwill of $431,000 and intangible assets of $80,000, a portion of which is deductible for tax purposes.
NOTE K – RECENT ACCOUNTING PRONOUNCEMENTS
In June 2006, the Financial Accounting Standards Board (“FASB”) issued Interpretation No. 48, “Accounting for Uncertainty in Income Taxes” – an interpretation of FASB Statement No. 109, “Accounting for Income Taxes” (“FIN 48”), which clarifies the accounting for uncertainty in income taxes. FIN 48 prescribes a recognition threshold and measurement attribute for the financial statement recognition and measurement of a tax position taken or expected to be

108


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS — UNAUDITED (continued)
March 31,September 30, 2006
NOTE IKSEGMENT INFORMATIONRECENT ACCOUNTING PRONOUNCEMENTS – (continued)
Segment assets and the basis of segmentation are consistent withtaken in a tax return. The interpretation requires that reported at June 30, 2005. Segment information for sales and income from operations are as follows:
                 
  Three months ended March 31,  Nine months ended March 31, 
  2006  2005  2006  2005 
Net sales                
Hyaluronan products $5,347,000  $5,034,000  $14,639,000  $14,205,000 
Oral restorative products  11,428,000   9,213,000   30,770,000   26,565,000 
             
  $16,775,000  $14,247,000  $45,409,000  $40,770,000 
             
Income from operations                
Hyaluronan products $1,493,000  $1,020,000  $3,547,000  $3,192,000 
Oral restorative products  1,948,000   1,084,000   3,649,000   2,767,000 
             
  $3,441,000  $2,104,000  $7,196,000  $5,959,000 
             
NOTE J — ACQUISITION OF BARDO-BIOTECH SAS
Effective August 12, 2005, the Company acquired 100% of the stock of Bardo-Biotech SAS, a privately-owned distributor of the Company’s Oral Restorative products located in Beauzelle, France. The Company included the operating results of Bardo-Biotech SASrecognize in the financial statements from August 1, 2005.the impact of a tax position. Recognition is allowed if the tax position is more likely than not to be sustained on audit, based on the technical merits of the position. FIN 48 also provides guidance on derecognition, classification, interest and penalties, accounting in interim periods and disclosure. The provisions of FIN 48 are effective for fiscal years beginning after December 15, 2006 with the cumulative effect of the change in accounting principle recorded as an adjustment to opening retained earnings. The adoption of this statement is not expected to have a material impact on the Company’s consolidated financial position or results of operations.
In conjunction with this acquisition,September 2006, the consideration paidSEC staff issued Staff Accounting Bulletin No. 108, “Considering the Effects of Prior Year Misstatements when Quantifying Misstatements in Current Year Financial Statements.” SAB 108 was $401,000 in cashissued to provide consistency between how registrants quantify financial statement misstatements and $362,000 in debt forgiveness. The acquisition resulted in estimated goodwillis effective for fiscal years ending after November 15, 2006.
SAB 108 established an approach that requires quantification of $518,000 pending completionfinancial statement misstatements based on the effects of the final determination of intangible asset allocation, a portion of which is deductible for tax purposes. Approximately $43,000misstatement on each of the purchase price was placed incompany’s financial statements and the related financial statement disclosures. This approach is commonly referred to as the “dual approach” because it requires quantification of errors under both the roll-over and iron curtain methods. The initial application of SAB 108 is not expected to have a bank guarantee account inmaterial impact on the event there are any loss claimsCompany’s consolidated financial position or asset valuation adjustments that arise.results of operations.
NOTE KLAGREEMENTSLEGAL PROCEEDINGS
On September 20, 2004,Lifecore was named as a defendant in 80 product liability lawsuits. The lawsuits alleged that the Company secured worldwide marketing rightsplaintiffs suffered injuries due to its ferric hyaluronan adhesion prevention product from Ethicon, Inc. The Company’s product, which was previously marketed by Gynecare (“Gynecare”), a divisionthe defective nature of Ethicon, Inc. (“ETHICON”), under the trademark GYNECARE INTERGEL Adhesion Prevention Solution (“INTERGEL Solution”) which was manufactured by Lifecore and marketed by ETHICON, Inc. The other defendants in these lawsuits were ETHICON, Inc., which was voluntarily withdrawn fromLifecore’s exclusive worldwide marketing partner for INTERGEL Solution through its division, GYNECARE Worldwide, and Johnson & Johnson, the market by Gynecare on March 27, 2003parent company of ETHICON. Many of the lawsuits also named Vital Pharma, Inc. as a defendant; Vital Pharma acted as the contract packager for the INTERGEL solution. The plaintiffs in these actions were individuals who were patients in medical procedures during which INTERGEL Solution was used and who were allegedly injured due to assess information obtained from its usagethe defective nature of INTERGEL Solution.
ETHICON accepted Lifecore’s tender of the defense of these lawsuits under The Conveyance, License, Development and Supply Agreement between the parties, subject to a reservation of rights, and ETHICON defended Lifecore in all of these matters. Lifecore accepted Vital Pharma’s tender of the treatmentdefense of patients. Underthese lawsuits under the Supply Agreement between Lifecore and Vital Pharma, subject to a reservation of rights. Lifecore’s insurer, Federal Insurance, has paid for Vital Pharma’s defense. Lifecore has also asserted that ETHICON is obligated to pay for Vital Pharma’s defense costs, pursuant to the agreement Gynecare will have no responsibilitybetween ETHICON and Lifecore.
On September 20, 2006, settlement documents relating to all but one of the lawsuits remaining at that date were executed on behalf of the parties. The terms of the settlement do not call for any aspect of the future manufacture, marketing, sale or distribution of the product nor will it derive any financial benefit therefrom. Acash payment of $250,000, included in other income, was received during the second quarter of fiscal 2005 from Ethicon in conjunction with the above mentioned agreement.by Lifecore.

119


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS (continued)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS — UNAUDITED (continued)
March 31,September 30, 2006
NOTE L – LEGAL PROCEEDINGS – (continued)
TheOn September 25, 2006, Vital Pharma, Inc. and its insurer, Noetic Specialty Insurance Company, is named as a defendant in 67 pending lawsuits, all of which allege that the plaintiffs suffered injuries due to the defective nature of INTERGEL Solution manufactured bysued the Company and marketed by ETHICON. Underits insurer, Federal Insurance Company. Vital Pharma and Noetic are seeking reimbursement of legal fees and expenses incurred in the terms of its Conveyance, License, DevelopmentINTERGEL litigation, and Supply Agreement dated August 8, 1994 with ETHICON, ETHICON isa declaration that the Company and Federal are obligated to fully indemnify and hold the CompanyVital Pharma harmless from all claims relatedwith respect to the sale and use of INTERGEL Solution, unless it is ultimately determined that a plaintiff’s injuries were caused by a breach of the Company’s limited contractual warranty to ETHICON.litigation. The Company believes that ETHICON is obligated to fully indemnify the Company in connection with all of the pendingVital Pharma’s and Noetic’s claims relating to INTERGEL Solution. The Company also has product liability insurance that it believes would cover its exposure, if any, related to these claims.have no merit.
NOTE M – RECLASSIFICATIONS
Certain 2005 amounts have been reclassified to conform to the 2006 presentation.

1210


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
Critical Accounting Policies
The discussion and analysis of our financial condition and results of operations are based upon the Company’s consolidated financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States. The preparation of these financial statements requires management to make estimates and assumptions in certain circumstances that affect the reported amount of assets and liabilities, revenues and expenses, and related disclosure of contingent assets and liabilities at the date of the Company’s financial statements. Management bases its estimates and judgments on historical experience, observance of trends in the industry, information provided by customers and other outside sources and on various other factors that are believed to be reasonable under the circumstances. Actual results may differ from these estimates under different assumptions or conditions.
Revenue Recognition:
The Company recognizes revenue when the product is shipped or otherwise accepted by unaffiliated customers, pursuant to customerscustomers’ orders, the price is fixed and collection is reasonably assured. The Securities and Exchange Commission’s Staff Accounting Bulletin (“SAB”) No. 101, “Revenue Recognition,” provides guidance on the application of generally accepted accounting principles to selected revenue recognition issues. The Company has concluded that its revenue recognition policy is appropriate and in accordance with generally accepted accounting principles and SAB No. 101.
Allowance for Uncollectible Accounts Receivable:
Accounts receivable are reduced by an allowance for amounts that may become uncollectible in the future. The Company extends credit to customers in the normal course of business but generally does not require collateral or any other security to support amounts due. Management performs on-going credit evaluations of the Company’s customers and bases the estimated allowance on these evaluations.
Inventories:
Inventories are stated at the lower of cost (first-in, first-out method) or market and have been reduced to the lower of cost or market for obsolete, excess or unmarketable inventory. The lower of cost or market adjustment is based on management’s review of inventories on hand compared to estimated future usage and sales.
Goodwill, Intangibles and Other Long-Lived Assets:
Intangibles and certain other long-lived assets with a definite life are amortized over their useful lives. Useful lives are based on management’s estimates of the period that the assets will generate revenue.
The Company reviews goodwill for impairment on an annual basis or upon a triggering event.
Management has reviewed goodwill and other intangibles for impairment and has concluded that such assets are appropriately valued at the financial statement dates.

1311


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
Accounting for Income Taxes:
Income taxes are accounted for under the provisions of Statement of Financial Accounting Standards No. 109 (“SFAS 109”), “Accounting for Income Taxes.” Under this method, deferred tax assets and liabilities are determined based upon the difference between the financial statement and tax bases of assets and liabilities using the enacted tax rates in effect for the year in which the differences are expected to affect taxable income. The tax consequences of events recognized in the current year’s financial statements are included in determining income taxes currently payable. However, because tax laws and financial accounting standards differ in their recognition and measurement of assets, liabilities, equity, revenue, expenses, gains and losses, differences arise between the amount of taxable income and pretax financial income for a year and between the tax bases of assets or liabilities and their reported amounts in the financial statements. Because it is assumed that the reported amounts of assets and liabilities will be recovered and settled, respectively, a difference between the tax basis of an asset or a liability and its reported amount in the balance sheet will result in a taxable or a deductible amount in some future years when the related liabilities are settled or the reported amounts of the assets are recovered, hence giving rise to a deferred tax asset. Management must then assess the likelihood that the deferred tax assets will be recovered from future taxable income and, to the extent that recovery is not likely, a valuation allowance must be established.
In fiscal 2005, management determined that it was appropriate to release a substantial portion of the deferred tax valuation allowance based upon the Company’s then-current and expected level of profitability, and the belief that it was more likely than not that the deferred tax assets would be utilized before they expired. The remaining valuation allowance is provided for foreign net operating losses. As part of the process of preparing the consolidated financial statements, income taxes are required to be estimated. This process involves estimating actual current tax exposure together with assessing temporary differences that may result in deferred tax assets or liabilities. Management judgment is required in determining any valuation allowance recorded against deferred tax assets. Any such valuation allowance would be based on management’s estimates of future taxable income and the period over which deferred tax assets would be recoverable.
Stock-based compensation:
On July 1, 2005, the Company adopted Statement of Financial Accounting Standard No. 123(R), “Share-based Payment” (SFAS 123(R)”),SFAS 123R, which requires the fair values of all share-based payment transactions, including grants of stock options, to be recognized in the income statement as an operating expense, based on the fair values over the requisite service period. The computation of fair value and the related stock compensation expense involves numerous estimates and assumptions based on historical experience and utilizes valuation models which are designed to produce estimated fair value based on these estimates and assumptions.

14


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
Overview
The Company manufactures biomaterials and medical devices for use in various surgical markets and provides related specialized contract aseptic manufacturing services. The Company operates through two business units, the Hyaluronan Division and the Oral RestorativeDental Division.
The Company’s Hyaluronan Division is principally involved in the development and manufacture of products utilizing hyaluronan, a naturally occurring polysaccharide that is widely distributed in the extracellular matrix of connective tissues in both animals and humans.
The Hyaluronan Division primarily sells into three medical segments: 1) Ophthalmic, 2) Orthopedic, and 3) Veterinary. In addition, the Company developed and owns the global marketing rights for a product using its patented ferric hyaluronan adhesion prevention technology. The product, FeHA, (formerly labeled as GYNECARE INTERGEL Adhesion Prevention Solution), has been clinically proven to reduce the incidence of post-surgical adhesions following surgical trauma. The product was voluntarily withdrawn from the market in March 2003 in order to assess information obtained from postmarketing experience with the product. The Company is currently evaluating regulatory requirements and opportunities for distribution partners to market the FeHA product.
The Company also supplies hyaluronan to customers pursuing other medical applications, such as wound care, aesthetic surgery, medical device coatings, tissue engineering, drug delivery and pharmaceuticals. The Company leverages its hyaluronan manufacturing expertise to provide expanded hyaluronan product offerings and specialized aseptic manufacturing of hyaluronan products.

12


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
The Company’s Oral RestorativeDental Division develops and markets precision surgical and prosthetic devices for the restoration of damaged or deteriorating dentition and associated support tissues. The Company’s dental implants are permanently implanted in the jaw for tooth replacement therapy as long-term support for crowns, bridges and dentures.
The Oral RestorativeDental Division also offers innovative bone regenerative products for the repair of bone defects resulting from periodontal disease and tooth loss. Additionally, the Oral RestorativeDental Division provides professional support services to its dental surgery clients through comprehensive education curricula provided in the Company’s various Support PlusÔ programs and surgical courses. These professional continuing education programs are designed to train restorative clinicians and their auxiliary teams in the principles of tooth replacement therapy and practice management. The Company’s Increasing Case Acceptance Program (“ICA”) offers clients the marketing and consultative tools and training to foster higher patient acceptance of dental implants.
The Oral RestorativeDental Division’s products are marketed in the United States through the Company’s direct sales force. Internationally, the Division’s products are marketed through direct subsidiaries in Italy, Germany, France and Sweden, and through 25 international distributors covering 3749 additional countries.
Acquisition of Bardo-Biotech SAS
EffectiveOn August 12, 2005, the Company acquired 100% of the stock of Bardo-Biotech SAS, a privately-owned distributor of the Company’s Oral RestorativeDental products located in Beauzelle, France. The Company included the operating results of Bardo-Biotech SAS in the financial statements from August 1, 2005.2005, the effective date.
In conjunction with this acquisition, the consideration paid was $401,000 in cash and $362,000 in debt forgiveness. The acquisition resulted in estimated goodwill of $518,000 pending completion$431,000 and intangible assets of the final determination of intangible asset allocation,$80,000, a portion of which is deductible for tax purposes. Approximately $43,000 of the purchase price was placed in a bank guarantee account in the event there are any loss claims or asset valuation adjustments that arise.

1513


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
Results of Operations
Three Months Ended March 31,September 30, 2006 Compared to Three Months Ended March 31,September 30, 2005:
                                                
 Hyaluronan Oral Restorative    Hyaluronan Dental   
 Division Division Consolidated  Division Division Consolidated 
 2006 2005 2006 2005 2006 2005  2006 2005 2006 2005 2006 2005 
Net sales $5,347,000 $5,034,000 $11,428,000 $9,213,000 $16,775,000 $14,247,000  $4,779,000 $4,661,000 $10,231,000 $8,764,000 $15,010,000 $13,425,000 
Cost of goods sold 2,449,000 2,317,000 3,759,000 3,270,000 6,208,000 5,587,000  2,122,000 2,059,000 3,450,000 3,015,000 5,572,000 5,074,000 
                          
Gross profit 2,898,000 2,717,000 7,669,000 5,943,000 10,567,000 8,660,000  2,657,000 2,602,000 6,781,000 5,749,000 9,438,000 8,351,000 
  
Operating expenses  
Research and development 516,000 952,000 365,000 283,000 881,000 1,235,000  716,000 620,000 380,000 394,000 1,096,000 1,014,000 
Marketing and sales 149,000 133,000 4,376,000 3,528,000 4,525,000 3,661,000  196,000 183,000 4,716,000 3,881,000 4,912,000 4,064,000 
General and administrative 740,000 612,000 980,000 1,048,000 1,720,000 1,660,000  749,000 661,000 1,175,000 1,045,000 1,924,000 1,706,000 
                          
 1,405,000 1,697,000 5,721,000 4,859,000 7,126,000 6,556,000  1,661,000 1,464,000 6,271,000 5,320,000 7,932,000 6,784,000 
                          
  
Operating income $1,493,000 $1,020,000 $1,948,000 $1,084,000 $3,441,000 $2,104,000  $996,000 $1,138,000 $510,000 $429,000 $1,506,000 $1,567,000 
                          
Net Sales. Net sales for the quarter ended March 31,September 30, 2006 increased $2,528,000$1,585,000 or 18%12% as compared to the same quarter of last fiscal year. Hyaluronan Division sales increased $313,000$118,000 or 6%3%, and Oral RestorativeDental Division sales increased $2,215,000$1,467,000 or 24%17%.
Hyaluronan Division sales for the current quarter increased to $5,347,000$4,779,000 from $5,034,000$4,661,000 in the same quarter of last fiscal year due to increased sales to veterinaryorthopedic customers and increased revenue from product development activities offset partially by lower sales to orthopedicophthalmic customers.
Oral RestorativeDental Division sales for the current quarter increased to $11,428,000$10,231,000 from $9,213,000$8,764,000 in the same quarter of last fiscal year. Domestic sales increased 28%16% due to the addition of sales representatives sales of the RENOVA Internal Hex Implant System and sales of the newly launched PrimaTM Implant System. International sales increased 20%18% due to sales of the RESTORE External Hex Implant System, sales of the PrimaPrima™ Implant System and the subsidiary in France, which was acquired in August 2005.sales growth by our subsidiaries.
Gross profit. Consolidated gross profit, as a percentage of net sales, was 63% in the current quarter and 61%62% in the same quarter of last fiscal year.
The gross profit for the Hyaluronan Division was 54%56% in the current quarter and also 54%56% in the same quarter of last fiscal year.
Gross profit for the Oral RestorativeDental Division increased to 67%was 66% in the current quarter from 65%and also 66% in the same quarter of last fiscal year primarily due to product mix and higher average selling prices.year.
Research and development. Consolidated research and development expenses consist of personnel costs, contract services, facility and equipment charges and materials consumed in the development of new products or the research and testing of enhancements to existing products. Research and development activities include: pilot plant operations, development of new formulations, design and testing of new products, regulatory services and clinical evaluation. Research and development expenses decreased $354,000increased $82,000 or 29%8% in the current quarter as compared to the same quarter last fiscal year. The decreaseincrease is primarily due to lower regulatory consulting expensesan increase in the Hyaluronan Division.stock-based compensation.

1614


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
Marketing and sales. Consolidated marketing and sales expenses increased by $864,000$848,000 or 24%21% in the current quarter as compared to the same quarter of last fiscal year. The increase was due mainly to costs associated with the launchaddition of the new Prima Implant System, the expansion of the oral restorative’s10 domestic sales forcerepresentatives, expanded marketing activities and international operations and compensation expense associated withincurring expenses for an entire quarter at the adoptionFrance subsidiary compared to incurring expenses for just two months in the same quarter of SFAS 123R.last fiscal year.
General and administrative. Consolidated general and administrative expenses increased by $60,000$218,000 or 4%13% in the current quarter as compared to the same quarter of last fiscal year. The increase was due to stock-based compensation expense associated withincurring expenses for an entire quarter at the adoptionFrance subsidiary compared to incurring expenses for just two months in the same quarter of SFAS 123R.last fiscal year, and an increase in benefits and information systems expenses.
Other income (expense). Net other income, as shown on the Consolidated Statements of Operations, increased $10,000$305,000 for the current quarter as compared to the same quarter of last fiscal year. The increase was primarily due to an increase in interest income of $136,000$196,000 resulting from a higher cash balance offset by decreasesand higher interest rates and an increase in currency transaction gains realized on Euro denominated intercompany transactions of $122,000.$97,000.
Provision for income taxes.Provision for income taxes was $1,391,000$713,000 at an effective rate of 38.5% and $129,000$563,000 at an effective rate of 35% for the three monthsmonth periods ended March 31,September 30, 2006 and 2005, respectively. The effective rate for the prior year period was significantly lower than the comparable periods in fiscal 2006 due to recognizing a tax benefit for the partial release in the deferred tax asset valuation allowance for the net operating losses utilized in the prior year period. As a result, the Company’s statement of earnings reflects more normal tax charges throughout fiscal 2006 and beyond. However, with the exception of the Alternative Minimum Tax and certain state taxes, the Company will not use cash for domestic income taxes until its net operating losses are fully realized on its tax returns. The Company accounts for income taxes under the provisions of SFAS 109, “Accounting for Income Taxes.”
Under this method, deferred tax assets and liabilities are determined based on the difference between the financial statement and tax bases of assets and liabilities using the enacted tax rates in effect for the year in which the differences are expected to affect taxable income. The Company believes that in fiscal 2006 its tax rate will be approximately 38%, even though the actual amount of taxes paid will be reduced significantly by the utilization of the net operating loss carryforward.

17


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
Nine Months Ended March 31, 2006 Compared to Nine Months Ended March 31, 2005
                         
  Hyaluronan  Oral Restorative    
  Division  Division  Consolidated 
  2006  2005  2006  2005  2006  2005 
Net sales $14,639,000  $14,205,000  $30,770,000  $26,565,000  $45,409,000  $40,770,000 
Cost of goods sold  6,858,000   6,518,000   10,541,000   9,620,000   17,399,000   16,138,000 
                   
Gross profit  7,781,000   7,687,000   20,229,000   16,945,000   28,010,000   24,632,000 
                         
Operating expenses                        
Research and development  1,728,000   2,451,000   1,150,000   803,000   2,878,000   3,254,000 
Marketing and sales  433,000   375,000   12,228,000   10,338,000   12,661,000   10,713,000 
General and administrative  2,073,000   1,669,000   3,202,000   3,037,000   5,275,000   4,706,000 
                   
   4,234,000   4,495,000   16,580,000   14,178,000   20,814,000   18,673,000 
                   
                         
Operating income $3,547,000  $3,192,000  $3,649,000  $2,767,000  $7,196,000  $5,959,000 
                   
Net Sales. Net sales for the nine months ended March 31, 2006 increased $4,639,000 or 11% as compared to the same period of last fiscal year. Hyaluronan Division sales increased $434,000 or 3%, and Oral Restorative Division sales increased $4,205,000 or 16%.
Hyaluronan Division sales for the current period increased to $14,639,000 from $14,205,000 in the same period of last fiscal year due to increased sales to veterinary customers and from product development offset partially by lower sales to ophthalmic customers.
Oral Restorative Division sales for the current period increased to $30,770,000 from $26,565,000 in the same period of last fiscal year. Domestic sales increased 21% due to the addition of sales representatives, sales of the RENOVA Internal Hex Implant System and sales of the newly launched Prima Implant System. International sales increased 10% due to sales of the RESTORE External Hex Implant System, sales of the Prima Implant System and the subsidiary in France, which was acquired in August 2005.
Gross profit. Consolidated gross profit, as a percentage of net sales, was 62% in the current period and 60% in the same period of last fiscal year.
The gross profit for the Hyaluronan Division decreased to 53% in the current period from 54% in the same period of last fiscal year; a 2.1 percentage point decrease was due to an increase in unused manufacturing capacity charges associated with decreased hyaluronan production, offset by a 1.1 percentage point increase due to product mix.
Gross profit for the Oral Restorative Division increased to 66% in the current period from 64% in the same period of last fiscal year of which 1.2 percentage points were due to a favorable shift in sales mix from lower margin products to higher margin products and 0.8 percentage points were due to fixed costs spread over a larger sales base.
Research and development. Consolidated research and development expenses consist of personnel costs, contract services, facility and equipment charges and materials consumed in the development of new products or enhancements to existing products. Research and development activities include: pilot plant operations, development of new formulations, design and testing of new products, regulatory services and clinical evaluation. Research and development expenses decreased $376,000 or 12% in the current period as compared to the same period last fiscal year. The decrease is due to lower regulatory consulting expenses in the Hyaluronan Division.

18


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
Marketing and sales. Consolidated marketing and sales expenses increased by $1,948,000 or 18% in the current period as compared to the same period of last fiscal year. The increase was due mainly to costs associated with the launch of the new Prima Implant System, the expansion of the oral restorative’s domestic sales force and international operations and stock-based compensation expense associated with the adoption of SFAS 123R.
General and administrative. Consolidated general and administrative expenses increased by $569,000 or 12% in the current period as compared to the same period of last fiscal year. The increase is related to $328,000 of stock-based compensation expense associated with the adoption of SFAS 123R and higher insurance costs.
Other income (expense). Net other income, as shown on the Consolidated Statements of Operations, increased $60,000 for the current period as compared to the same period of last fiscal year. The increase was primarily due to bond retirement expense of $290,000 in the 2005 period and an increase in interest income of $386,000 resulting from a higher cash balance and higher interest rates, offset by decreases in currency transaction gains realized on Euro denominated intercompany transactions of $393,000 and the Ethicon, Inc. payment of $250,000 received during the second quarter of fiscal 2005.
Provision for income taxes.Provision for income taxes was $2,794,000 and $359,000 for the nine months ended March 31, 2006 and 2005, respectively. The effective rate for the prior year period was significantly lower than the comparable periods in fiscal 2006 due to recognizing a tax benefit for the partial release in the deferred tax asset valuation allowance for the net operating losses utilized in the prior year period. As a result, the Company’s statement of earnings reflects more normal tax charges throughout fiscal 2006 and beyond. However, withWith the exception of the Alternative Minimum Tax and certain state taxes, the Company will not use cash for domestic income taxes until its net operating losses are fully realized on its tax returns.
The Company accounts for income taxes under the provisions of SFAS 109, “Accounting for Income Taxes.” Under this method, deferred tax assets and liabilities are determined based on the difference between the financial statement and tax bases of assets and liabilities using the enacted tax rates in effect for the year in which the differences are expected to affect taxable income. The Company believes that in fiscal 2006 its tax rate will be approximately 38%, even though the actual amount of taxes paid will be reduced significantly by the utilization of the net operating loss carryforward.

1915


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
Liquidity and Capital Resources
The Company’s Annual Report on Form 10-K, as amended, for the year ended JuneAs of September 30, 2005 contains a detailed discussion of the Company’s liquidity and capital resources. Investors should read the 2005 Form 10-K, as amended, in conjunction with this Quarterly Report on Form
10-Q.
For the nine month period ended March 31, 2006, the Company had positive$28.1 million of cash and cash equivalents and working capital of $53.9 million. Cash and cash equivalents increased during the three month period ended September 30, 2006 by $1.5 million.
Cash Provided by Operating Activities.Operating cash flow for the three month period ended September 30, 2006 was primarily the result of $3,626,000 dueoperational profitability. Net cash provided by operations was approximately $1.6 million, attributable to operating activities. The Company had positivenet income of $1.1 million and adjustments for non-cash charges related to the changes in deferred tax assets of $0.6 million and depreciation and amortization of $0.5 million. Inventories increased $0.6 million and accrued liabilities decreased $0.5 million, which were partially offset by a decrease in accounts receivable of $0.5 million.
Net cash flowprovided by operations in the same period of last fiscal yearsyear was approximately $0.2 million, attributable to net income of $1.0 million and adjustments for non-cash charges related to the changes in deferred tax assets of $0.5 million and depreciation and amortization of $0.5 million. Inventories increased $1.5 million and accrued liabilities decreased by $0.5 million.
Cash Used in Investing Activities. Net cash used in investing activities was $0.3 million and $0.8 million in the three month periods ended September 30, 2006 and 2005, 2004respectively. Cash used in investing activities reflected purchases of property and 2003. Chargesequipment of $0.3 million and $0.4 million in the three month periods ended September 30, 2006 and 2005, respectively. Net cash of $0.3 million was used for unused manufacturing capacity associated withthe acquisition of the stock of the Company’s hyaluronan production have continued to negatively impact operating resultsFrench distributor in the currentsame period of last fiscal year. Also, marketing
Cash Provided by Financing Activities. Net cash provided by financing activities was $0.1 million and sales expenses for$0.6 million in the oral restorative products are expectedthree month periods ended September 30, 2006 and 2005, respectively. Cash provided was attributable to continue at a high level due to continued international expansionproceeds from the exercise of stock options of $0.2 million and increased personnel costs associated with expanding$0.7 million in the sales force.three month periods ended September 30, 2006 and 2005, respectively.
The Company has a $5,000,000 credit facility with a bank which has a maturity date of December 31, 2006. The agreement allows for advances against eligible accounts receivable, subject to compliance with covenants. Under the credit facility, interest will accrue at the prime rate minus .5% or LIBOR plus 2.25%, at the Company’s option. At March 31,September 30, 2006 and June 30, 2005,2006, there were no balances outstanding under the line of credit.
On August 19, 2004, the Company issued variable rate industrial revenue bonds. The proceeds from these bonds were used to retire the existing 10.25% fixed rate industrial revenue bonds on September 1, 2004. The aggregate principal amount of the new bonds was $5,630,000, and the bonds bear interest at a variable rate set weekly by the bond remarketing agent (3.36%(3.93% as of March 31,September 30, 2006). In addition, the Company pays an annual remarketing fee equal to .125% and an annual letter of credit fee of 1.0%. The bonds are collateralized by a bank letter of credit which is secured by a first mortgage on the facility. The Company is required to make monthly principal and interest payments to a sinking fund. The terms of the agreement require the Company to comply with various financial covenants including minimum tangible net worth, liabilities to tangible net worth ratio and net income (loss). As of March 31,September 30, 2006 and June 30, 2005,2006, the Company was in compliance with all covenants.

16


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
The Company’s ability to generate positive cash flow from operations and achieve ongoing profitability is dependent upon the continued expansion of revenue from its hyaluronan and oral restorativedental businesses. Growth in the Hyaluronan Division is unpredictable due to the complex governmental regulatory environment for new medical products, the early stage of certain of these markets and the uncertainty associated with the future market status of the Company’s adhesion prevention product. Similarly, expansion of the Company’s Oral RestorativeDental Division sales is also dependent upon increased revenue from new and existing customers, as well as successfully competing in a more mature market. The Company expects its current cash balance, cash generated from anticipated operations and the available funds under the line of credit to satisfy cash flow needs in the near term. No assurance can be given that the Company will maintain positive cash flow from operations. While the Company’s capital resources appear adequate today, the Company may seek additional financing in the future. If additional financing is necessary, no assurance can be given that such financing will be available and, if available, will be on terms favorable to the Company and its shareholders.
The Company does not have any material “off-balance sheet” financing activities.
Seasonality
The Company’s oral restorativedental business is seasonal in nature. Historically, sales for the Oral RestorativeDental Division are lower in the first quarter than throughout the rest of the year, as a result of European holidays during the summer months.

20


LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS
OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS (continued)
Cautionary Statement
Statements included in this Management’s Discussion and Analysis of Financial Condition and Results of Operations and elsewhere in this Form 10-Q, in future filings by the Company with the Securities and Exchange Commission and in the Company’s press releases and oral statements made with the approval of authorized executive officers, that are not historical or current facts, should be considered “forward-looking statements” made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements may, among other things, relate to market acceptance and demand for the Company’s products, future product development plans and timing, the results of clinical trials, FDA clearances and the related timing of such, the potential size of the markets for the Company’s products, future product introductions, future revenues, expense levels, tax rates and capital needs and the Company’s ability to successfully negotiate acceptable agreements with its corporate partners. These statements are subject to certain risks and uncertainties that could cause actual results to differ materially from historical earnings and those presently anticipated or projected. The Company wishes to caution readers not to place undue reliance on any such forward-looking statements, which speak only as of the date made. The following important factors, among others, in some cases have affected or in the future could affect the Company’s actual results and could cause its actual financial performance to differ materially from that expressed in any forward-looking statement: (1) obtaining the necessary regulatory approvals for new hyaluronan and oral restorativedental products; (2) the Company’s reliance on corporate partners to develop new products on a timely basis and to market the Company’s existing and new hyaluronan products effectively; (3) intense competition in the markets for the Company’s principal products; and (4) the uncertainty associated with the future market status of the Company’s adhesion prevention product. Investors are referred to a more detailed discussion of the risks presented in Exhibit 99.1 toPart I, Item 1A of the Company’s Annual Report on Form 10-K as amended, for the fiscal year ended June 30, 2005.2006.

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LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART I — FINANCIAL INFORMATION
ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
The Company invests its excess cash in money market mutual funds and bank certificates of deposits and highly rated short-term corporate debt securities.deposits. All investments are held to maturity. The market risk on such investments is minimal.
Receivables from sales to foreign customers are denominated in U.S. dollars. Transactions at the Company’s foreign subsidiaries are denominated in European Euros at Lifecore Biomedical SpA, Lifecore Biomedical GmbH and Lifecore Biomedical SAS and are denominated in Swedish Krona at Lifecore Biomedical AB. The Company is exposed to foreign currency exchange rate risk arising from transactions in the normal course of business from sales to its foreign subsidiaries. Because the Company’s products are manufactured or sourced primarily from the United States, a stronger U.S. dollar generally has a negative impact on results from operations outside the United States while a weaker dollar generally has a positive effect. The Company does not use derivative financial instruments to manage foreign currency fluctuation risk.
On August 19, 2004, the Company issued variable rate industrial revenue bonds. The proceeds from these bonds were used to retire the existing 10.25% fixed rate industrial revenue bonds on September 1, 2004. The aggregate principal amount of the new bonds was $5,630,000, and the bonds bear interest at a variable rate set weekly by the bond remarketing agent (3.36%(3.93% as of March 31,September 30, 2006). A ten percent change in this variable rate would result in approximately $17,000$20,000 of additional interest expense annually.
ITEM 4. CONTROLS AND PROCEDURES
(a) Evaluation of disclosure controls and procedures.
Under the supervision and with the participation of the Company’s management, including the Company’s Chief Executive Officer and Chief Financial Officer, the Company evaluated the effectiveness of the design and operation of the Company’s disclosure controls and procedures (as defined in Rule 13a – 15(e) under the Securities Exchange Act of 1934, as amended, (the “Exchange Act”)). Based upon that evaluation, the Chief Executive Officer and Chief Financial Officer concluded that, as of the end of the period covered by this report, the Company’s disclosure controls and procedures were effective.
(b) Changes in internal control over financial reporting.
During the fiscal period covered by this report, there has been no change in the Company’s internal control over financial reporting (as defined in Rule 13a – 15(f) under the Exchange Act) that has materially affected, or is reasonably likely to materially affect, the Company’s internal control over financial reporting.

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LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART II — OTHER INFORMATION
ITEM 1. LEGAL PROCEEDINGS
The Company isLifecore Biomedical, Inc. (the “Company”) was named as a defendant in 67 currently pending lawsuits, involving alleged injuries to 69 women. Fifty-five of the pending cases are proceeding in Florida state court. The balance of the pending lawsuits have been filed in various states including California, Louisiana, Minnesota, New Jersey, Pennsylvania and Wisconsin. Lifecore is aware that five cases have been settled by Ethicon. Another eight plaintiffs have voluntarily dismissed their claims. One case,Shumbo-Poissant v. Ethicon, Inc., et al. (Conn.), was dismissed on summary judgment.
80 product liability lawsuits. The lawsuits allegealleged that the plaintiffs suffered injuries due to the defective nature of GYNECARE INTERGEL Adhesion Prevention Solution (“INTERGEL Solution”) which was developed and manufactured by the Company.Company and marketed by ETHICON, Inc. The other defendants in these lawsuits arewere ETHICON, Inc., which was the Company’s exclusive worldwide marketing partner for INTERGEL Solution through its division, GYNECARE Worldwide, and Johnson & Johnson, the parent company of ETHICON. MostMany of the lawsuits also namenamed Vital Pharma, Inc. as a defendant; Vital Pharma acted as the contract packager for the INTERGEL Solution.solution. The plaintiffs in these actions arewere individuals who were patients in medical procedures during which INTERGEL Solution was used and who were allegedly injured due to the defective nature of INTERGEL Solution.
On September 20, 2006, settlement documents relating to all but one of the lawsuits remaining at that date were executed on behalf of the parties. The Company had previously anticipated thatterms of the settlement do not call for any cash payment by the Company. Since the execution of the settlement documents, Lifecore has been sued in one additional lawsuit, captionedfiled in Nebraska. As of this date, there are two cases remaining:Renee ContrattoBrandy R. Kreifel and Tammy Lyden v. Gynecare, Inc., Ethicon, Inc., Lifecore Biomedical, Inc. and Johnson & Johnson Company;Stephanie and Michael Stibor and Wisconsin Physicians Service Insurance Corporation v. Ethicon, Inc., d/b/a Gynecare Worldwide, Johnson & Johnson, Lifecore Biomedical, Inc. and Vital Pharma, IncKrista Jacobson. (N.D. Cal.) would beAlthough the first lawsuit to go to trial. The trial of that matter has been delayed, and is now set for January 2007. Defendants have filed motions to exclude the plaintiff’s expert testimony, and motions for summary judgment seeking dismissalvast majority of the Contratto matter on various legal grounds. Those motions are pending beforeINTERGEL claims have been resolved, there can be no assurance that other related claims will not arise.
ETHICON defended the Court. The Florida lawsuits are scheduled for a mandatory mediation involvingCompany in all of the Florida cases during the last week of June 2006. The first-filed Florida case,Black v. Ethicon, Inc., et al., is currently scheduled for trial in the fall of 2006, if the mediation is unsuccessful.
ETHICON began marketing INTERGEL Solution outside the United States in June 1998 for reducing the incidence of post-surgical adhesions. INTERGEL Solution was approved by the FDA for the U.S. market in November 2001. INTERGEL Solution was voluntarily withdrawn from the market by ETHICON in March 2003 in order to assess information obtained from post-marketing experience with the product, including allegations of adverse events associated with off-label use in non-conservative surgical procedures (such as hysterectomies).
ETHICONthese lawsuits and is defending the Company in all of thesethe two remaining lawsuits. Under the terms of the Company’s Conveyance, License, Development and Supply Agreement dated August 8, 1994 with ETHICON, ETHICON is obligated to indemnify and hold the Company harmless from all claims related to the sale and use of INTERGEL Solution, unless it is ultimately determined that a plaintiff’s injuries were caused by a breach of the Company’s limited contractual warranty to ETHICON under that agreement. The Company believes that ETHICON will be obligated to fully indemnify the Company in connection with all of the pendingany remaining claims relating to INTERGEL Solution.Solution sold prior to its voluntary market withdrawal in March 2003.
PursuantOn September 25, 2006, Vital Pharma, Inc. and its insurer, Noetic Specialty Insurance Company, sued the Company and its insurer, Federal Insurance Company, in Palm Beach County, Florida. Federal has removed the case to federal court, and the Company’s answer is currently scheduled to be filed on November 6, 2006. Vital Pharma and Noetic contend that the Company has breached the terms of its agreement withthe Supply Agreement between the Company and Vital Pharma, by failing to fully defend and indemnify Vital Pharma in the Company’s insurer is coveringIntergel lawsuits. Vital Pharma and Noetic are seeking reimbursement of legal fees and expenses incurred in the INTERGEL litigation, and a declaration that the Company and Federal are obligated to fully indemnify and hold Vital Pharma harmless with respect to the Intergel litigation.
The Company believes that Vital Pharma’s and Noetic’s claims have no merit. The Company complied with its obligations under the Supply Agreement. The Company agreed to pay for the costs of Vital Pharma’s defense, costs. This has been done withsubject to a full reservation of rightsrights. The Company, through its insurer, Federal, did pay for the reasonable costs and expenses incurred by Vital Pharma during the Company.INTERGEL litigation. Although Vital Pharma did complain, during the course of the INTERGEL litigation, that Federal did not pay all of the costs and expenses incurred, Vital Pharma did not provide any basis to challenge the amounts not paid by Federal pursuant to Federal’s bill auditing process. The Company has also asserted that tendered the defense of this matter to Federal, and Federal has agreed to defend the Company subject to a reservation of rights.
ETHICON is obligatedbegan marketing INTERGEL Solution outside the United States in June 1998 for reducing the incidence of post-surgical adhesions. INTERGEL Solution was approved by the FDA for the U.S. market in November 2001. INTERGEL Solution was voluntarily withdrawn from the market by ETHICON in March 2003 in order to pay for Vital Pharma’s defense costs, pursuant toassess information obtained from postmarketing experience with the agreement between ETHICON and the Company.
The Company has also received four claim letters alleging claims similar to the lawsuits. ETHICON is responding to the claim letters on behalfproduct, including allegations of the Company.adverse events associated with off-label use in non-conservative surgical procedures (such as hysterectomies).

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LIFECORE BIOMEDICAL, INC. AND SUBSIDIARIES
PART II — OTHER INFORMATION
ITEM 6. EXHIBITS
3.1 Amended and Restated Articles of Incorporation, as adopted on January 18, 2006 (incorporated by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K filed on January 24, 2006)
 
3.2 Amended Bylaws, as adopted on January 18, 2006 (incorporated by reference to Exhibit 3.2 to the Company’s Current Report on Form 8-K filed on January 24, 2006)
 
4.1 Form of Common Stock Certificate (incorporated by reference to Exhibit 4.1 to 1987 S-2 Registration Statement [File No. 33-12970])
 
4.2 Form of Rights Agreement, dated as of May 23, 1996, between the Company and Norwest Bank Minnesota, National Association (incorporated by reference to Exhibit 1 to the Company’s Form 8-A Registration Statement dated May 31, 1996)
 
10.1 1996 Stock Option Plan, as amended to date.
10.2Fiscal Year 2007 Bonus Plan, effective July 1, 2006 (incorporated by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K filed on September 19, 2006)
 
31.1 Certification of the Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
 
31.2 Certification of the Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
 
32.1 Certification of the Chief Executive Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
 
32.2 Certification of the Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002

2420


SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
     
 LIFECORE BIOMEDICAL, INC.

By:
Dated: November 9, 2006 /s/ Dennis J. Allingham   
 Dennis J. Allingham  
By:
Dated: May 10, 2006/s/ Dennis J. Allingham
Dennis J. Allingham
 President, Chief Executive Officer, Secretary and Director
(duly authorized officer) 
 (duly authorized officer)
   
Dated: May 10,November 9, 2006 /s/ David M. Noel   
 David M. Noel  
David M. Noel
 Vice President of Finance and Chief Financial Officer

(principal financial and accounting officer)

2521


Exhibit Index
3.1 Amended and Restated Articles of Incorporation, as adopted on January 18, 2006 (incorporated by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K filed on January 24, 2006)
 
3.2 Amended Bylaws, as adopted on January 18, 2006 (incorporated by reference to Exhibit 3.2 to the Company’s Current Report on Form 8-K filed on January 24, 2006)
 
4.1 Form of Common Stock Certificate (incorporated by reference to Exhibit 4.1 to 1987 S-2 Registration Statement [File No. 33-12970])
 
4.2 Form of Rights Agreement, dated as of May 23, 1996, between the Company and Norwest Bank Minnesota, National Association (incorporated by reference to Exhibit 1 to the Company’s Form 8-A Registration Statement dated May 31, 1996)
 
10.1 1996 Stock Option Plan, as amended to date.
10.2Fiscal Year 2007 Bonus Plan, effective July 1, 2006 (incorporated by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K filed on September 19, 2006)
 
31.1 Certification of the Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
 
31.2 Certification of the Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
 
32.1 Certification of the Chief Executive Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
 
32.2 Certification of the Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
 
32.2 Certification of the Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002

2622