ICAD INC - Quarter Report: 2010 June (Form 10-Q)

 

 

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM 10-Q

(Mark One)

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

		For the quarterly period ended June 30, 2010

OR

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 1-9341

iCAD, Inc.

Delaware		02-0377419
(State or other jurisdiction		(I.R.S. Employer Identification No.)
of incorporation or organization)

98 Spit Brook Road, Suite 100, Nashua, NH		03062
(Address of principal executive offices)		(Zip Code)

(603) 882-5200

Not Applicable

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 requirement for the past 90 days. YES þ NO o.

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). YES o NO o.

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 “large accelerated filer”, “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act.

Large Accelerated filer o		Accelerated filer o		Non-accelerated filer o		Smaller reporting company þ
				(do not check if a smaller reporting company)

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act) YES o NO þ.

As of the close of business on August 3, 2010 there were 45,939,063 shares outstanding of the registrant’s Common Stock, $.01 par value.

 

 

iCAD, INC.

INDEX

		PAGE
PART I FINANCIAL INFORMATION
Item 1 Financial Statements (unaudited)
Balance Sheets as of June 30, 2010 and December 31, 2009			3
Statements of Operations for the three and six month periods ended June 30, 2010 and 2009			4
Statements of Cash Flows for the six month periods ended June 30, 2010 and 2009			5
Notes to Consolidated Financial Statements			6–10
Item 2 Management’s Discussion and Analysis of Financial Condition and Results of Operations			11–17
Item 3 Quantitative and Qualitative Disclosures about Market Risk			17
Item 4 Controls and Procedures			17
PART II OTHER INFORMATION
Item 2 Unregistered Sales of Equity Securities and Use of Proceeds			18
Item 6 Exhibits			19
Signatures			20
Exhibit 31.1
Exhibit 31.2
Exhibit 32.1
Exhibit 32.2

iCAD, Inc.

Balance Sheets

(unaudited)

		June 30,				December 31,
		2010				2009
Assets
Current assets:
Cash and cash equivalents		$	17,196,502			$	16,248,031
Trade accounts receivable, net of allowance for doubtful accounts of $50,000 in 2010 and $84,000 in 2009			4,152,492				4,692,614
Inventory, net			865,347				1,094,115
Prepaid expenses and other current assets			440,257				393,490
Total current assets			22,654,598				22,428,250
Property and equipment:
Equipment			2,821,671				2,873,012
Leasehold improvements			74,107				72,612
Furniture and fixtures			344,700				344,700
Marketing assets			292,613				292,613
			3,533,091				3,582,937
Less accumulated depreciation and amortization			2,774,944				2,661,083
Net property and equipment			758,147				921,854
Other assets:
Deposits			32,126				63,194
Patents, net of accumulated amortization			118,605				90,027
Customer relationships, net of accumulated amortization			184,065				200,407
Technology intangibles, net of accumulated amortization			5,538,855				6,093,294
Tradename, net of accumulated amortization			86,800				99,200
Goodwill			43,515,285				43,515,285
Total other assets			49,475,736				50,061,407
Total assets		$	72,888,481			$	73,411,511
Liabilities and Stockholders’ Equity
Current liabilities:
Accounts payable		$	734,706			$	1,365,558
Accrued salaries and other expenses			2,712,466				2,199,286
Deferred revenue			3,568,463				3,139,567
Total current liabilities			7,015,635				6,704,411
Long-term warranty expense			19,173				23,275
Long-term deferred revenue			521,472				375,183
Total liabilities			7,556,280				7,102,869
Commitments and contingencies (Note 5)
Stockholders’ equity:
Preferred stock, $ .01 par value: authorized 1,000,000 shares; none issued			—				—
Common stock, $ .01 par value: authorized 85,000,000 shares; issued 45,896,929 in 2010 and 45,746,736 in 2009; outstanding 45,829,053 in 2010 and 45,678,860 in 2009			458,969				457,467
Additional paid-in capital			151,005,516				150,062,733
Accumulated deficit			(85,182,020	)			(83,261,294	)
Treasury stock at cost (67,876 shares)			(950,264	)			(950,264	)
Total stockholders’ equity			65,332,201				66,308,642
Total liabilities and stockholders’ equity		$	72,888,481			$	73,411,511

See accompanying notes to consolidated financial statements.

iCAD, INC.

Statements of Operations

(unaudited)

		Three Months Ended								Six Months Ended
		June 30,								June 30,
		2010				2009				2010				2009
Revenue
Products		$	4,716,434			$	4,822,094			$	9,928,086			$	11,161,715
Service and supplies			1,380,878				907,793				2,689,722				1,733,170
Total revenue			6,097,312				5,729,887				12,617,808				12,894,885
Cost of revenue
Products			557,155				893,086				1,224,635				1,950,987
Service and supplies			165,919				160,131				346,024				359,034
Total cost of revenue			723,074				1,053,217				1,570,659				2,310,021
Gross margin			5,374,238				4,676,670				11,047,149				10,584,864
Operating expenses:
Engineering and product development			1,525,346				1,738,278				3,081,472				3,899,493
Marketing and sales			3,041,584				2,652,312				5,874,747				5,597,433
General and administrative			1,839,908				1,716,083				4,326,153				3,551,394
Total operating expenses			6,406,838				6,106,673				13,282,372				13,048,320
Loss from operations			(1,032,600	)			(1,430,003	)			(2,235,223	)			(2,463,456	)
Other income			275,000				—				275,000				—
Interest income — net			21,481				30,750				39,497				65,676
Net loss		$	(736,119	)		$	(1,399,253	)		$	(1,920,726	)		$	(2,397,780	)
Net loss per share:
Basic and Diluted		$	(0.02	)		$	(0.03	)		$	(0.04	)		$	(0.05	)
Weighted average number of shares used in computing loss per share:
Basic and Diluted			45,736,520				45,412,573				45,711,541				45,382,928

See accompanying notes to consolidated financial statements.

iCAD, INC.

Statements of Cash Flows

(unaudited)

		Six Months Ended				Six Months Ended
		June 30, 2010				June 30, 2009
Cash flows from operating activities:
Net loss		$	(1,920,726	)		$	(2,397,780	)
Adjustments to reconcile net loss to net cash provided by operating activities:
Depreciation			248,618				432,349
Amortization			583,181				584,386
Gain on sale of patent			(275,000	)			—
Stock-based compensation			980,865				1,002,722
Changes in operating assets and liabilities:
Accounts receivable			540,122				2,188,980
Inventory			228,768				(30,712	)
Prepaid expenses, other current assets and deposits			(15,699	)			17,207
Accounts payable			(630,852	)			(730,272	)
Accrued salaries, warranty and other expenses			509,078				(1,142,698	)
Deferred revenue			575,185				293,785
Total adjustments			2,744,266				2,615,747
Net cash provided by operating activities			823,540				217,967
Cash flows from investing activities:
Additions to patents, technology and other			(28,578	)			(99,467	)
Additions to property and equipment			(84,911	)			(62,118	)
Proceeds from sale of patent			275,000				—
Net cash provided by (used for) investing activities			161,511				(161,585	)
Cash flows from financing activities:
Issuance of common stock for cash			—				3,201
Taxes paid related to restricted stock issuance			(36,580	)			—
Net cash provided by (used for) financing activities			(36,580	)			3,201
Increase in cash and equivalents			948,471				59,583
Cash and equivalents, beginning of period			16,248,031				13,115,715
Cash and equivalents, end of period		$	17,196,502			$	13,175,298

See accompanying notes to consolidated financial statements.

iCAD, INC.

(1)

Basis of Presentation and Significant Accounting Policies

Reference should be made to iCAD, Inc.’s (“iCAD”, “Company”, “we”, “our” or “us”) Annual Report on Form 10-K for the year ended December 31, 2009 for a comprehensive summary of significant accounting policies.

The accompanying consolidated financial statements of the Company have been prepared in accordance with accounting principles generally accepted in the United States of America (“generally accepted accounting principles”). In the opinion of management, these unaudited interim consolidated financial statements reflect all adjustments, consisting of normal recurring adjustments, necessary for a fair presentation of the financial position at June 30, 2010, the results of operations for the three and six month periods ended June 30, 2010 and 2009, and cash flows for the six month periods ended June 30, 2010 and 2009. Although the Company believes that the disclosures in these financial statements are adequate to make the information presented not misleading, certain information normally included in the footnotes prepared in accordance with generally accepted accounting principles has been omitted as permitted by the rules and regulations of the Securities and Exchange Commission (“SEC”). The accompanying financial statements should be read in conjunction with the audited financial statements and notes thereto included in the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2009 filed with the SEC on March 23, 2010. The results for the three and six month periods ended June 30, 2010 are not necessarily indicative of the results that may be expected for the fiscal year ending December 31, 2010, or any future period. Interim period amounts are not necessarily indicative of the results of operations for the full fiscal year.

In February 2010, the Financial Accounting Standards Board (“FASB”) issued ASU 2010-09, Subsequent Events (Topic 855) – Amendments to Certain Recognition and Disclosure Requirements (“ASU 2010-09”). ASU 2010-09 requires an entity that is an SEC filer to evaluate subsequent events through the date that the financial statements are issued and removes the requirement that an SEC filer disclose the date through which subsequent events have been evaluated. ASC 2010-09 was effective upon issuance. The adoption of this standard had no effect on our results of operation or our financial position.

iCAD, INC.
Notes to Consolidated Financial Statements
(Unaudited)
June 30, 2010

(2)

Net Loss per Common Share

The Company’s basic net loss per common share is computed by dividing net loss by the weighted average number of shares of common stock outstanding for the period. Since the Company has a net loss for all periods presented, the effect of all potentially dilutive securities, such as common stock equivalents, is anti-dilutive. Common stock equivalent shares consist of common shares issuable upon the exercise of stock options and warrants and vesting of restricted stock. Accordingly, basic and diluted net loss per share is the same for all periods presented. As of June 30, 2010 and 2009, there were 6,184,351 and 6,853,626 shares of common stock, respectively, issuable upon the exercise of stock options and warrants and vesting of restricted stock, which were excluded from the calculation as their effect would have been antidilutive.

(3)

Stock-Based Compensation

The Company follows FASB Accounting Standards Codification (“ASC”) Topic 718, “Compensation – Stock Compensation”, (“ASC 718”), for all share-based compensation that was not vested as of January 1, 2006. Under this application, the Company is required to record compensation expense for all awards granted after the date of adoption and for the unvested portion of previously granted awards that remain outstanding at the date of adoption.

The Company issued 530,500 shares of restricted stock and 128,318 stock options in the six months ended June 30, 2010. The restricted stock granted during the first six months of 2010 had a weighted average value of $1.41 per share. The options granted during the first six months of 2010 had a weighted average exercise price of $1.58 per share. The weighted average fair value of options granted during this six month period was $0.64 per share and was estimated on the grant date using the Black-Scholes option-pricing model with the following weighted average assumptions: expected volatility of 68.34%, expected term of 3.5 years, risk-free interest rate of 2.41%, and expected dividend yield of 0%. The average expected life was calculated using the Company’s historical average life. The risk-free rate is based on the rate of U.S. Treasury zero-coupon issues with a remaining term equal to the expected life of option grants. The Company recorded $980,865 for share-based compensation for the six months ended June 30, 2010.

iCAD, INC.
Notes to Consolidated Financial Statements
(Unaudited)
June 30, 2010

(3)

Stock-Based Compensation (continued)

For the same period in 2009, the Company issued 169,483 stock options. The Company did not issue any shares of restricted stock during this six month period in 2009. The options granted during the first six months of 2009 had a weighted average exercise price of $1.13 per share. The weighted average fair value of options granted during the six month period ended June 30, 2009 was $0.42 per share and was estimated on the grant date using the Black-Scholes option-pricing model with the following weighted average assumptions: expected volatility of 62.8%, expected term of 3.5 years, risk-free interest rate of 1.69%, and expected dividend yield of 0%. The Company recorded $1,002,722 for share-based compensation for the six months ended June 30, 2009.

As of June 30, 2010 there was approximately $1,413,000 of total unrecognized compensation cost related to unvested options and restricted stock. That cost is expected to be recognized over a weighted average period of three years.

The Company’s aggregate intrinsic value of options outstanding at June 30, 2010 was $827,190. The aggregate intrinsic value of restricted stock outstanding at June 30, 2010 was $1,781,541.

(4)

Fair Value Measurements

FASB ASC Topic 820, “Fair Value Measurement and Disclosures”, (“ASC 820”) defines fair value, establishes a framework for measuring fair value under generally accepted accounting principles and enhances disclosures about fair value measurements. Fair value is defined under ASC 820 as the exchange price that would be received for an asset or paid to transfer a liability (an exit price) in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants on the measurement date. Valuation techniques used to measure fair value under ASC 820 must maximize the use of observable inputs and minimize the use of unobservable inputs. The standard describes a fair value hierarchy based on three levels of inputs, of which the first two are considered observable and the last unobservable, that may be used to measure fair value which are the following:

•

Level 1 — Quoted prices in active markets for identical assets or liabilities.

	•		Level 2 — Inputs other than Level 1 that are observable, either directly or indirectly, such as quoted prices for similar assets or liabilities; quoted prices in markets that are not active; or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities.
	•		Level 3 — Unobservable inputs that are supported by little or no market activity and that are significant to the fair value.

iCAD, INC.
Notes to Consolidated Financial Statements
(Unaudited)

(4)

Fair Value Measurements (continued)

A financial instrument’s level within the fair value hierarchy is based on the lowest level of any input that is significant to the fair value measurement.

In accordance with ASC 820, the Company’s financial assets that are measured at fair value on a recurring basis as of June 30, 2010 are cash equivalents. The cash equivalents are measured using level one inputs.

(5)

Commitments and Contingencies

In July 2007, a dissolved former Canadian subsidiary of the Company, CADx Medical Systems Inc. (“CADx Medical”), received a tax re-assessment of approximately $6,800,000 from the Canada Revenue Agency (“CRA”) resulting from CRA’s audit of CADx Medical’s Canadian federal tax return for the year ended December 31, 2002. In February 2010, the CRA reviewed the matter and reduced the tax re-assessment to approximately $703,000, excluding interest and penalties. The CRA has the right to pursue the matter until July 2017. The Company believes that it is not liable for the re-assessment against CADx Medical and no accrual was recorded as of June 30, 2010.

(6)

Income Taxes

At June 30, 2010, the Company had no material unrecognized tax benefits and no adjustments to liabilities or operations were required under ASC 740, “Income Taxes”. The Company does not expect that the unrecognized tax benefits will materially increase within the next twelve months. The Company did not recognize any interest or penalties related to uncertain tax positions at June 30, 2010. The Company files United States federal income tax returns and income tax returns in various states and local jurisdictions. On July 8, 2010, the Company was notified by the Internal Revenue Service of its intent to examine the tax returns for the 2008 tax year. Management cannot reasonably determine the results of this examination, if any, at this time. The Company is not under examination for any additional open tax years by the Internal Revenue Service or any other state and federal jurisdictions.

iCAD, INC.
Notes to Consolidated Financial Statements
(Unaudited)

(7)

Goodwill

In accordance with FASB ASC Topic 350-20, “Intangibles — Goodwill and Other”, (“ASC 350-20”), the Company tests goodwill for impairment on an annual basis and between annual tests if events and circumstances indicate it is more likely than not that the fair value of the Company is less than its carrying value. Events that would indicate impairment and trigger an interim impairment assessment include, but are not limited to, current economic and market conditions, changes in its results of operations and changes in its forecasts or market expectation relating to future results.

The Company’s goodwill arose in connection with its acquisitions in June 2002 and in December 2003. The Company operates in one segment and as one reporting unit since its products perform the same basic function, have common sales channels and/or resellers, and are developed and supported by one central staff. Therefore, the Company uses market capitalization as the best evidence of fair value (market capitalization is calculated using the quoted closing share price of the Company’s common stock at its annual impairment date of October 1, multiplied by the number of common shares outstanding) of the Company. The Company tests goodwill for impairment by comparing its market capitalization (fair value) to its carrying value. The fair value of the Company is compared to the carrying amount at the same date as the basis to determine if an impairment exists. The Company performed the step one fair value comparison as of October 1, 2009 and the Company’s market capitalization exceeded its carrying value. At June 30, 2010, the Company’s market capitalization exceeded its carrying value.

(8)

Recent Accounting Pronouncements

Effective January 1, 2009, the Company adopted guidance now codified as FASB ASC Topic 805, “Business Combinations” (“ASC 805”). This topic requires an acquirer to recognize and measure the identifiable assets acquired, the liabilities assumed, and any non-controlling interest in the acquiree at their fair values as of the acquisition date. The topic requires acquisition costs and any restructuring costs associated with the business combination to be recognized separately from the fair value of the business combination.

ASC 805 establishes requirements for recognizing and measuring goodwill acquired in the business combination or a gain from a bargain purchase as well as disclosure requirements designed to enable users to better interpret the results of the business combination. Early adoption of this topic was not permitted. The adoption of ASC 805 will impact the Company’s financial position, results of operations and cash flows to the extent it conducts acquisition-related activities and/or consummates business combinations. In the first six months of 2010, the Company recorded expenses of approximately $751,000 primarily related to a potential acquisition that was not consummated.

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

“Safe Harbor” Statement under the Private Securities Litigation Reform Act of 1995: Certain information included in this Item 2 and elsewhere in this Form 10-Q that are not historical facts contain forward looking statements that involve a number of known and unknown risks, uncertainties and other factors that could cause the actual results, performance or achievements of the Company to be materially different from any future results, performance or achievement expressed or implied by such forward looking statements. These risks and uncertainties include, but are not limited to, uncertainty of future sales levels, protection of patents and other proprietary rights, the impact of supply and manufacturing constraints or difficulties, product market acceptance, possible technological obsolescence of products, increased competition, litigation and/or government regulation, changes in Medicare reimbursement policies, competitive factors, the effects of a decline in the economy in markets served by the Company and other risks detailed in the Company’s other filings with the SEC. The words “believe”, “demonstrate”, “intend”, “expect”, “estimate”, “anticipate”, “likely”, “seek”, “should” and similar expressions identify forward-looking statements. Readers are cautioned not to place undue reliance on those forward-looking statements, which speak only as of the date the statement was made.

Results of Operations

Overview

iCAD is an industry-leading provider of advanced image analysis and workflow solutions that enable radiologists and other healthcare professionals to better serve patients by identifying pathologies and pinpointing cancer earlier. iCAD offers a comprehensive range of high-performance, expandable Computer-Aided Detection (CAD) systems and workflow solutions for mammography (film-based, digital radiography (DR) and computed radiography (CR), Magnetic Resonance Imaging (MRI), and Computed Tomography (CT)). iCAD’s solutions aid in the early detection of the most prevalent cancers including breast, prostate and colon cancer. Early detection of cancer is the key to better prognosis, less invasive and lower treatment costs, and higher survival rates. Performed as an adjunct to mammography screening, CAD has quickly become the standard of care in breast cancer detection, helping radiologists improve clinical outcomes while enhancing workflow. Computer-enhanced breast and prostate MRI analysis streamlines case interpretation workflow and generates more robust information for more effective patient treatment. CAD for mammography screening is also reimbursable in the U.S. under federal and most third-party insurance programs. Since receiving approval from the U.S. Food and Drug Administration (“FDA”) for the Company’s first breast cancer detection product in January 2002, over thirty eight hundred of iCAD’s CAD systems have been placed in mammography practices worldwide. iCAD is the only stand alone company offering CAD solutions for the early detection of breast cancer.

iCAD’s CAD mammography products have been shown to detect up to 72 percent of the cancers that biopsy proved were missed on the previous mammogram, an average of 15 months earlier. Our advanced pattern recognition technology analyzes images to identify patterns and then uses sophisticated mathematical analysis to mark suspicious areas.

The Company’s CAD systems include proprietary algorithm and other technology together with standard computer and display equipment. CAD systems for the film-based analog mammography market also include a radiographic film digitizer, either manufactured by the Company or others for the digitization of film-based medical images.

The Company intends to apply its core competencies in pattern recognition and algorithm development in disease detection to its future product development efforts. Its focus is on the development and marketing of cancer detection products for disease states where there are established or emerging protocols for screening as a standard of care. iCAD expects to pursue development or acquisition of products for select disease states that demonstrate one or more of the following: it is clinically proven that screening has a significant positive impact on patient outcomes, where there is an opportunity to lower health care costs, where screening is non-invasive or minimally invasive and where public awareness is high. The Company also intends to pursue opportunities beyond CAD through possible strategic acquisitions as part of its growth strategy, as such the Company continues to actively evaluate strategic opportunities in adjacent markets that could leverage its opportunities for growth beyond its historic core markets.

iCAD has applied its patented detection technology and algorithms to the development of CAD solutions for use with virtual colonoscopy or CT Colonography (CTC) to improve the detection of colonic polyps. The Company’s pattern recognition and image analysis expertise are readily applicable to colonic polyp detection and the Company has developed a CTC CAD solution. Virtual colonoscopy (CTC) is a technology that has evolved rapidly in recent years. Based on the results of the National CT Colonography trial, the Company expects that the market for virtual colonoscopy will grow along with the procedures for early detection of colon cancer. This trial demonstrated that CTC is highly accurate for the detection of intermediate and large polyps and that the accuracy of CTC is similar to a colonoscopy. CT Colonography or CTC is emerging as an alternative imaging procedure for evaluation of the colon. The Company has developed VeralookÔ, a product for computer aided detection of polyps in the colon using CTC and completed the clinical testing of its CTC CAD product in the first quarter of 2009. The Company filed a 510(k) application with the FDA in May 2009 seeking FDA clearance to market Veralook in the U.S. and received FDA clearance on August 4, 2010. Colorectal cancer has been shown to be highly preventable with early detection and removal of polyps.

In July 2008, the Company acquired pharmaco-kinetic based CAD products that aid in the interpretation of contrast enhanced MRI images of the breast and prostate and began marketing these products in the fourth quarter of 2008. The interpretation of MRI exams also benefits from advanced image analysis and clinical decision support tools. MRI is an excellent tool to detect breast cancer as well as prostate cancer. While MRI is a more expensive option than traditional mammography, it enables physicians to view tumors which may have been missed during routine screenings. MRI uses magnets and radio waves instead of x-rays to produce very detailed, cross-sectional images of the body, and can be used to look specifically at those areas.

The Company’s headquarters are located in Nashua, New Hampshire, with manufacturing and contract manufacturing facilities in New Hampshire and Massachusetts and a research and development facility in Ohio.

Critical Accounting Policies

The Company’s discussion and analysis of its financial condition, results of operations, and cash flows are based on the Company’s consolidated financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States of America. The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses, and related disclosure of contingent assets and liabilities. On an on-going basis, we evaluate these estimates, including those related to accounts receivable allowance, inventory valuation and obsolescence, intangible assets, income taxes, warranty obligations, contingencies and litigation. Additionally, the Company uses assumptions and estimates in calculations to determine stock-based compensation. The Company bases its estimates on historical experience and on various other assumptions that it believes to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions.

The Company’s critical accounting policies are set forth in its Annual Report on Form 10-K for the fiscal year ended December 31, 2009. The Company believes that revenue recognition is a critical accounting policy because it is governed by multiple complex accounting rules; however, there are no significant estimates or assumptions used in recording the Company’s revenue.

Quarter Ended June 30, 2010 compared to Quarter Ended June 30, 2009 and Six Months Ended June 30, 2010 compared to Six Months Ended June 30, 2009

Revenue. Total revenue for the three month period ended June 30, 2010 was $6,097,312 compared with revenue of $5,729,887 for the three month period ended June 30, 2009, for an increase of $367,425 or 6.4%. Total revenue for the six month period ended June 30, 2010 was $12,617,808 compared with revenue of $12,894,885 for the six month period ended June 30, 2009, for a slight decrease of $277,077 or 2.1%. These results for the three and six month periods were due primarily to an increase in digital and MRI CAD revenue and in service and supply revenue, offset by a decline in film-based CAD revenue.

The Company’s digital and MRI CAD revenue for the second quarter of 2010 increased $891,921 or 28.8%, to $3,991,346, compared to revenue of $3,099,425 in the same period in 2009. Revenue during the second quarter of 2009 was particularly soft due to the weakened economy and budget freezes in healthcare capital spending. The Company’s digital and MRI CAD revenue for the six months ended June 30, 2010 increased $280,082 or 3.6%, to $8,156,628, compared to revenue of $7,876,546 in the same period in 2009.

Revenue from iCAD’s film based products for the three and six month periods ended June 30, 2010 decreased 57.9% and 46.1%, respectively, to $725,088 and $1,771,458, compared to $1,722,669 and $3,285,169 in the three and six month periods ended June 30, 2009. This decrease can be attributed to current economic conditions and deferred hospital spending, as the majority of film-based revenue is derived from sales of the Company’s TotalLook MammoAdvantage. The TotalLook MammoAdvantage product is used for digitizing film based prior mammography exams for comparative reading and is sold to further optimize workflow in a digital mammography environment. The TotalLook MammoAdvantage product is typically sold as customers are preparing to go digital. In addition, the demand for film-based products and accessories continues to decline as the marketplace continues to transition to digital technologies.

Service and supply revenue for the three and six month periods ended June 30, 2010 increased 52.1% and 55.2%, respectively, to $1,380,878 and $2,689,722, compared to $907,793 and $1,733,170 in the three and six month periods ended June 30, 2009. The increase in the Company’s service and supply revenue is due primarily to increased service contract revenue on the Company’s growing installed base of products as customers migrate from warranty to service contracts, and to renewed service contract agreements. Service contract revenue as a percentage of the Company’s total service and supply revenue for the three and six months ended June 30, 2010 represented 94% and 91%, respectively, compared to 92% and 93% for the same periods of 2009.

		Three months ended June 30,
		2010				2009				Change				% Change
Digital & MRI CAD revenue		$	3,991,346			$	3,099,425			$	891,921				28.8	%
Film based revenue			725,088				1,722,669				(997,581	)			-57.9	%
Service & supply revenue			1,380,878				907,793				473,085				52.1	%
Total revenue		$	6,097,312			$	5,729,887			$	367,425				6.4	%

		Six months ended June 30,
		2010				2009				Change				% Change
Digital & MRI CAD revenue		$	8,156,628			$	7,876,546			$	280,082				3.6	%
Film based revenue			1,771,458				3,285,169				(1,513,711	)			-46.1	%
Service & supply revenue			2,689,722				1,733,170				956,552				55.2	%
Total revenue		$	12,617,808			$	12,894,885			$	(277,077	)			-2.1	%

Gross Margin. Gross margin increased to 88.1% and 87.6% for the three and six month periods ended June 30, 2010 compared to 81.6% and 82.1%, respectively, in the same three and six month periods in 2009. The increase in total gross margin is primarily attributable to component cost reductions, the realization of some average selling price increases, overhead cost reduction efforts and lower repair costs related to service contracts on a growing installed base of digital products and the new TotalLook MammoAdvantage product. Gross margin on product revenue increased to 88.2% and 87.7% for the three and six months ended June 30, 2010 compared to 81.5% and 82.5%, respectively, in the same period in 2009. Gross margin on service and supply revenue increased to 88.0% and 87.1% for the three and six month periods ended June 30, 2010 compared to 82.4 and 79.3%, respectively, in the same three and six month periods in 2009.

Engineering and Product Development. Engineering and product development costs for the three and six month periods ended June 30, 2010 decreased by $212,932 or 12.2% and $818,021 or 21.0%, respectively, from $1,738,278 and $3,899,493 in 2009 to $1,525,346 and $3,081,472, respectively, in 2010. The decrease in engineering and product development costs during the three and six month periods ended June 30, 2010 was primarily due to decreases in compensation related expenses of $86,000 and $301,000, respectively, resulting primarily from staff reductions, and in consulting services of $28,000 and $340,000 principally relating to the licensing and clinical trial costs for the Company’s CT Colon product which was completed in the first quarter of 2009. In addition, during the three and six month periods, the Company recorded decreases in legal, depreciation and various other expenses totaling $99,000 and $177,000, respectively.

Marketing and Sales. Marketing and sales expense for the three and six month periods ended June 30, 2010 increased by $389,272 or 14.7% and $277,314 or 5.0%, respectively, from $2,652,312 and $5,597,433 in 2009 to $3,041,584 and $5,874,747, respectively, in 2010. The increase in marketing and sales expense during this three and six month period was primarily due to the increase of $252,000 and $278,000, respectively, in consulting services, an increase in compensation related expenses of $219,000 and $226,000, and in sales commissions of $62,000 and $41,000 due to the increase in revenue during the second quarter of 2010. These increases were offset by decreases in public relations, tradeshow, marketing, depreciation, and various administrative expenses totaling $144,000 and $268,000, respectively, for the three and six month periods ended June 30, 2010.

General and Administrative. General and administrative expenses for the three and six month periods ended June 30, 2010 increased by $123,825 or 7.2%, and $774,759 or 21.8%, respectively, from $1,716,083 and $3,551,394 in 2009 to $1,839,908 and $4,326,153, respectively, in 2010. The increase in general and administrative expense during this three and six month period of 2010 was due primarily to an increased bonus accrual of $184,000 and $189,000, respectively, and in legal and professional fees of $70,000 and $751,000 associated primarily with a potential acquisition that was not consummated. This increase in general and administrative expense was offset by decreases in consulting, legal, taxes and various other administrative expenses totaling $130,000 and $165,000, respectively, for the three and six month periods ended June 30, 2010.

Other Income: During the second quarter of 2010 the Company received a one-time payment of $275,000 related to the sale of a patent that was acquired as part of the Qualia Computing, Inc. acquisition in 2003. The patent is for technology that is outside of the medical device industry and unrelated to the Company’s core business.

Interest Income/Expense. Net interest income for the three and six month periods ended June 30, 2010 decreased by $9,269 and $26,179, respectively, from $30,750 and $65,676 in 2009 to $21,481 and $39,497 in the same period of 2010. The decrease in interest income is due primarily to the reduction of the interest rate earned from the Company’s money market accounts.

Net Loss. As a result of the foregoing, the Company recorded a net loss of ($736,119) or ($0.02) per share for the three month period ended June 30, 2010 on revenue of $6,097,312, compared to a net loss of ($1,399,253) or ($0.03) per share for the three month period ended June 30, 2009 on revenue of $5,729,887. The net loss for the six months ended June 30, 2010 was ($1,920,726) or ($0.04) per share on revenue of $12,617,808, compared to a net loss of ($2,397,780) or ($0.05) per share on revenue of $12,894,885 for the six months ended June 30, 2009.

Backlog. The Company’s product backlog (excluding service and supplies) as of June 30, 2010 totaled approximately $583,000 as compared to $511,000 at June 30, 2009 and $762,000 at March 31, 2010. It is expected that the majority of the backlog at June 30, 2010 will be shipped within the current fiscal year. Backlog as of any particular period should not be relied upon as indicative of the Company’s net revenues for any future period as a large amount of the Company’s product is booked and shipped within the same quarter.

Liquidity and Capital Resources

The Company believes that its current liquidity and capital resources are sufficient to sustain operations through at least the next 12 months, primarily due to cash on hand and projected cash balances from continuing operations. The Company’s ability to generate cash adequate to meet its future capital requirements will depend primarily on operating cash flow. If sales or cash collections are reduced from current expectations, or if expenses and cash requirements are increased, the Company may require additional financing, although there are no guarantees that the Company will be able to obtain the financing if necessary. We will continue to closely monitor our liquidity and the capital and credit markets.

At June 30, 2010, the Company had current assets of $22,654,598, current liabilities of $7,015,635 and working capital of $15,638,963. The ratio of current assets to current liabilities was 3.2:1.

Net cash provided by operating activities for the six months ended June 30, 2010 was $823,540, compared to net cash provided by operating activities of $217,967 for the same period in 2009. The cash provided by operating activities for the six months ended June 30, 2010 resulted from decreases in accounts receivable of $540,122, inventory of $228,768, accrued expenses of $509,078 and deferred revenue of $575,185, plus non-cash items including depreciation and amortization totaling $831,799 and stock based compensation of $980,865, which were offset by the net loss of $1,920,726, the gain on the sale of a patent of $275,000, an increase in prepaid expenses, other current assets and deposits of $15,699 and a decrease in accounts payable of $630,852.

The net cash provided by investing activities for the six months ended June 30, 2010 was $161,511, which consisted of proceeds from the sale of a patent of $275,000 offset by additions to patents, technology and other assets of $28,578 and additions to property and equipment of $84,911, compared to net cash used for investing activities for the six months ended June 30, 2009 of $161,585, which consisted of additions to patents, technology and other assets of $99,467 and additions to property and equipment of $62,118.

Net cash used for financing activities for the six months ended June 30, 2010 was $36,580 relating to taxes paid with respect to the issuance of restricted stock, compared to net cash provided by financing activities for the six months ended June 30, 2009 of $3,201 due to cash received from the issuance of common stock relating to the exercise of stock options.

Contractual Obligations

The following table summarizes, for the periods presented, the Company’s future estimated cash payments under existing contractual obligations at June 30, 2010.

		Payments due by period
						Less than 1
Contractual Obligations		Total				year				1-3 years				3-5 years				5+ years
Lease Obligations*		$	555,169			$	262,849			$	292,320			$	—			$	—
Total Contractual Obligations		$	555,169			$	262,849			$	292,320			$	—			$	—

Recent Accounting Pronouncements

Effective January 1, 2009, the Company adopted guidance now codified as FASB ASC Topic 805, “Business Combinations” (“ASC 805”). This topic requires an acquirer to recognize and measure the identifiable assets acquired, the liabilities assumed, and any non-controlling interest in the acquiree at their fair values as of the acquisition date. The topic requires acquisition costs and any restructuring costs associated with the business combination to be recognized separately from the fair value of the business combination. ASC 805 establishes requirements for recognizing and measuring goodwill acquired in the business combination or a gain from a bargain purchase as well as disclosure requirements designed to enable users to better interpret the results of the business combination. Early adoption of this topic was not permitted. The adoption of ASC 805 will impact the Company’s financial position, results of operations and cash flows to the extent it conducts acquisition-related activities and/or consummates business combinations. In the first six months of 2010, the Company recorded expenses of approximately $751,000 primarily related to a potential acquisition that was not consummated.

Item 3.		Quantitative and Qualitative Disclosures about Market Risk

Not applicable.

Item 4.		Controls and Procedures

The Company, under the supervision and with the participation of its management, including its principal executive officer and principal financial officer, evaluated the effectiveness of the design and operation of its disclosure controls and procedures as of the end of the period covered by this report. Based on this evaluation, the principal executive officer and principal financial officer concluded that the Company’s disclosure controls and procedures (as defined in Rule 13a-15(e) of the Securities Exchange Act of 1934 (”Exchange Act”)) were effective at the reasonable level of assurance.

A control system, no matter how well conceived and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met. Further, the design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues and instances of fraud, if any, within the Company have been detected. Because of the inherent limitations in a cost-effective control system, misstatements due to error or fraud may occur and not be detected. The Company conducts periodic evaluations to enhance, where necessary its procedures and controls.

The Company’s principal executive officer and principal financial officer conducted an evaluation of the Company’s internal control over financial reporting (as defined in Exchange Act Rule 13a-15(f)) to determine whether any changes in internal control over financial reporting occurred during the quarter ended June 30, 2010, that have materially affected or which are reasonably likely to materially affect internal control over financial reporting. Based on that evaluation, there has been no such change during such period.

PART II OTHER INFORMATION

Item 2.		Unregistered Sales of Equity Securities and Use of Proceeds

The following table represents information with respect to purchases of common stock made by the Company during the three months ended June 30, 2010:

										Total number
										of shares				Maximum
										purchased as				dollar value of
										part of publicly				shares that may
		Total number				Average				announced				yet be purchaed
		of shares				price paid per				plans or				under the plans
Month of purchase		purchased (1)				share				programs				or programs
April 1 - April 30, 2010			—			$	—			$	—			$	—
May 1 - May 31, 2010			—			$	—			$	—			$	—
June 1 - June 30, 2010			21,959			$	1.43			$	—			$	—
Total			21,959			$	1.43			$	—			$	—

Item 6.		Exhibits

Exhibit No.				Description
	31.1			Certification of Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
	31.2			Certification of Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
	32.1			Certification of Chief Executive Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
	32.2			Certification of Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

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.