8-K
Standard Biotools Inc. (LAB)
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 _____________________
Form 8-K _____________________
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date of Report (Date of earliest event Reported): May 7, 2020
Fluidigm Corporation (Exact Name of Registrant as Specified in Charter)
| Delaware | 001-34180 | 77-0513190 |
|---|---|---|
| (State or Other Jurisdiction of Incorporation) | (Commission File Number) | (I.R.S. Employer Identification Number) |
| 2 Tower Place, Suite 2000, South San Francisco, California 94080 | ||
| --- | ||
| (Address of Principal Executive Offices) (Zip Code) |
(650) 266-6000 (Registrant's telephone number, including area code)
(Former name or former address, if changed since last report)
| Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions: | ||
|---|---|---|
| [ ] | Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) | |
| [ ] | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) | |
| [ ] | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) | |
| [ ] | Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class | Trading Symbol(s) | Name of each exchange on which registered |
|---|---|---|
| Common stock, par value $0.001 per share | FLDM | Nasdaq Global Select Market |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (17 CFR §230.405) or Rule 12b-2 of the Securities Exchange Act of 1934 (17 CFR §240.12b-2). Emerging growth company [ ]
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. [ ]
Item 2.02. Results of Operations and Financial Condition.
On May 7, 2020, Fluidigm Corporation issued a press release reporting its financial results for the first fiscal quarter of 2020. A copy of the press release is furnished herewith as Exhibit 99.1.
The foregoing information in this Current Report on Form 8-K, including Exhibit 99.1 attached hereto, is being “furnished” and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, and shall not be incorporated by reference in any filing under the Securities Exchange Act of 1934, as amended, or the Securities Act of 1933, as amended, except as expressly set forth by specific reference in such future filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits.
| Exhibit No. | Description |
|---|---|
| 99.1 | Fluidigm Corporation Press Release dated May 7, 2020. |
SIGNATURE
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 hereunto duly authorized.
| Fluidigm Corporation | ||
|---|---|---|
| Date: May 7, 2020 | By: | /s/ Vikram Jog |
| Vikram Jog | ||
| Chief Financial Officer |
EdgarFiling
EXHIBIT 99.1
Fluidigm Announces First Quarter 2020 Financial Results
First Quarter Revenue Decreased 8 Percent to $27.6 Million
New COVID-19 Opportunities for Microfluidics and Mass Cytometry Businesses
Customers filing FDA Emergency Use Authorization for Ultrahigh-Throughput COVID-19 Tests on the BioMark platform
Maxpar Direct Immune Profiling Assay powering large COVID-19 Immune Function studies
SOUTH SAN FRANCISCO, Calif., May 07, 2020 (GLOBE NEWSWIRE) -- Fluidigm Corporation (Nasdaq:FLDM) today announced financial results for the first quarter ended March 31, 2020.
Financial Highlights
First Quarter 2020
- First quarter revenue decreased 8 percent to $27.6 million from $30.1 million. Total revenue included $3.1 million of license revenue.
- GAAP net loss for the quarter was $16.0 million, compared with a GAAP net loss of $25.5 million for the first quarter of 2019.
- Non-GAAP net loss was $9.4 million for the quarter, compared with a $8.2 million non-GAAP net loss for the first quarter of 2019.
“This is a different world from the one we knew a few months ago,” said Chris Linthwaite, Fluidigm President and CEO. “While the pandemic has created near-term headwinds, it has also delivered new opportunities. Our extremely high-throughput Biomark™ system enables labs to process up to 6,000 samples per day and is being employed in the global build-out of COVID-19 testing infrastructure. Our mass cytometry platform is measuring immune response in experimental new treatments and for characterization of COVID-19 induced immune response in the infected population. As a market leader in immune monitoring we are uniquely well-positioned to support testing of investigational new vaccines and therapeutics. I am impressed by our organization’s ability to adapt to the rapidly changing landscape.
“Protecting our employees, repositioning our products for COVID-19 applications and managing our liquidity are top priorities,” added Linthwaite. “From a liquidity perspective, we are focused on preserving the health of our business and actively managing our operating expenses in response to the evolving market conditions. Looking beyond this pandemic, our core business model is intact and we see incremental opportunities for new growth in the infectious disease market as the world returns to work. We anticipate infectious disease applications will complement our long-term commitment to biomarker discovery, disease research, and treatment paradigms linked to understanding immune function and response in a wide range of diseases.”
A reconciliation of GAAP to non-GAAP financial measures can be found in the tables of this news release.
First Quarter 2020 Results
Revenue by category:
| Category | Revenue by Category | Year-over-Year Change | % of Total Revenue | ||
|---|---|---|---|---|---|
| Instruments | $9.5 million | (26 | %) | 34 | % |
| Consumables | $9.5 million | (21 | %) | 34 | % |
| Service | $5.2 million | (2 | %) | 20 | % |
| License and Other | $3.4 million | N/A | 12 | % |
Revenue by market:
- Mass cytometry revenue decreased 20 percent to $15.0 million from $18.8 million in the prior year period. Mass cytometry product revenue decreased 26 percent to $11.5 million from $15.5 million in the prior year due to lower sales of instruments.
- Microfluidics revenue increased 11 percent to $12.6 million from $11.4 million in the prior year period. Microfluidics product revenue decreased 20 percent to $7.5 million from $9.4 million in the prior year period primarily due to lower sales of consumables partially offset by higher sales of instruments.
Revenue by geographic area:
| Geographic Area | Revenue by Geography | Year-over-Year Change | % of Total Revenue | ||
|---|---|---|---|---|---|
| Americas | $14.8 million | 14 | % | 54 | % |
| EMEA | $8.1 million | (1 | )% | 29 | % |
| Asia-Pacific | $4.7 million | (48 | %) | 17 | % |
Product and service margin:
Product and service margin was 53.8 percent in the first quarter of 2020 compared to 56.4 percent in the year ago period and 54.7 percent in the fourth quarter of 2019. Non-GAAP product and service margin was 67.3 percent in the first quarter of 2020 compared to 67.7 percent in the year ago period and 64.9 percent in the fourth quarter of 2019. The year-over-year decrease in product and service margin was primarily due to lower average selling prices and an unfavorable product mix, partially offset by lower service costs and improved manufacturing efficiencies. Sequentially, the increase in non-GAAP product and service margin was primarily due to lower service costs, favorable product mix, and lower inventory reserves. In the case of GAAP margin, the year-over-year decrease was coupled with fixed amortization over lower revenue. The decrease in sequential product and service margin was a result of fixed amortization over lower revenue more than offsetting lower service costs, favorable product mix, and lower inventory reserves.
Cash and cash equivalents, short-term investments, and restricted cash as of March 31, 2020:
Cash and cash equivalents, short-term investments, and restricted cash as of March 31, 2020, were $49.6 million. Cash and cash equivalents, short-term investments, and restricted cash as of December 31, 2019, were $60.7 million.
Operational and Business Progress
SARS-CoV-2 virus detection utilizing microfluidics
- OU Medicine has submitted a test to detect SARS-CoV-2, the virus that causes COVID‑19, for Emergency Use Authorization (EUA) by the U.S. Food and Drug Administration (FDA). This test is intended for large-scale testing of patients across the OU Medicine health care system and was developed in collaboration with University of Oklahoma Health Sciences Center and Oklahoma Medical Research Foundation.
- Lab 24, a contract research organization in Florida, has filed for FDA EUA for its SARS-CoV-2 detection test.
- BioXpedia, a contract research laboratory in Denmark, is offering SARS-CoV-2 testing on the Fluidigm Biomark HD system, with the capability to detect up to 24 total target genes per sample allowing testing for additional viral respiratory diseases.
Novel SARS-CoV-2 virus test utilizing microfluidics
- A consortium of medical schools led by the Icahn School of Medicine at Mount Sinai is developing a novel epigenetic test for early detection of SARS-CoV-2.
COVID-19 publications
- Fluidigm CyTOF^®^ technology, the Maxpar^®^ Direct™ Immune Profiling Assay™, and Maxpar Pathsetter™ analysis software were used in a clinical study to identify a distinct phenotype with an exaggerated immune response in critically ill patients with severe COVID-19.
- Imaging Mass Cytometry™ was used in a clinical study to identify and locate immune cells in lung tissue from patients who had COVID-19 and acute respiratory distress syndrome.
- Fluidigm CyTOF and microfluidics technologies were used by researchers at Beijing You’an Hospital for a multi-omic study. Researchers recently correlated mild and severe clinical data for COVID-19 patients upon admission and after initial treatment reflecting, differing gene expression patterns and T cell and cytokine levels.
- Fluidigm CyTOF technology was used in a clinical study producing preliminary evidence that stem cell therapy improves outcomes in patients with COVID-19 pneumonia, providing key information about potential mechanisms of action of the treatment strategy.
- Additional information on these publications can be found on our website at fluidigm.com.
Product launches, new services and acquisitions:
- Launched Therapeutic Insights Services, designed to provide researchers with sample-to-answer mass cytometry and Imaging Mass Cytometry service for a broad range of research needs including COVID-19 related research.
- Launched the AccuLift™ Laser Capture Microdissection System. The new AccuLift product portfolio enables precise and efficient capture of individual cells or larger tissue regions for DNA, RNA, and protein biomarker analysis.
- Acquired InstruNor AS to expand Fluidigm’s industry-leading mass cytometry capabilities and address flow cytometry markets with the addition of fully automated sample prep.
Conference Call Information
Fluidigm will host a conference call today, May 7, 2020, at 2:30 p.m. PT/5:30 p.m. ET to discuss first quarter 2020 financial results and operational progress. Individuals interested in listening to the conference call may do so by dialing the following:
US domestic callers: (877) 556-5248 Outside US callers: (720) 545-0029 Please reference Conference ID: 6873327
A live webcast of the conference call will be available online from the Investor Relations page of the Company’s website at Events & Presentations. The link will not be active until 2:15 p.m. PT/5:15 p.m. ET on May 7, 2020.
After the live webcast, the call will be archived on Fluidigm’s Investor Relations page at investors.fluidigm.com. In addition, a telephone replay of the teleconference will be available approximately 90 minutes after the end of the call.
The replay dial-in numbers are:
US domestic callers: (855) 859-2056 Outside US: (404) 537-3406 Please reference Conference ID: 6873327
The telephone replay will be available until May 14.
Statement Regarding Use of Non-GAAP Financial Information
Fluidigm has presented certain financial information in accordance with U.S. GAAP and also on a non-GAAP basis for the three-month periods ended March 31, 2020, and March 31, 2019. Management believes that non-GAAP financial measures, taken in conjunction with GAAP financial measures, provide useful information for both management and investors by excluding certain non-cash and other expenses that are not indicative of the company’s core operating results. Management uses non-GAAP measures to compare the company’s performance relative to forecasts and strategic plans and to benchmark the company’s performance externally against competitors. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used to supplement an understanding of the company’s operating results as reported under U.S. GAAP. Fluidigm encourages investors to carefully consider its results under GAAP, as well as its supplemental non-GAAP information and the reconciliation between these presentations, to more fully understand its business. Reconciliations between GAAP and non-GAAP operating results are presented in the accompanying tables of this release.
Use of Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including, among others, statements regardingopportunities for Fluidigm technology and products, including expected uses and demand for COVID-19 testing and research, potential for growth in revenues in the infectious disease markets, anticipated benefits of contractual relationships, including customers using Fluidigm technology for SARS-CoV-2 virus detection and epigenetic tests, and expectations for newly launched and recently acquired products and services. Forward‑looking statements are subject to numerous risks and uncertainties that could cause actual results to differ materially from currently anticipated results, including but not limited to the potential adverse effects of the coronavirus pandemic on our business and operating results during 2020; the suitability and acceptance of our tools and technology by the research community pursuing solutions for the novel coronavirus pandemic; our ability and/or the ability of the institutions utilizing our products and technology to obtain FDA and any other requisite approvals to use our products and technology for diagnostic testing purposes; customers and prospective customers continuing to curtail or suspend activities utilizing our products; interruptions or delays in the supply of components or materials for, or manufacturing of, our products resulting from the pandemic or other factors; challenges inherent in developing, manufacturing, launching, marketing, and selling new products; risks relating to reliance on sales of capital equipment for a significant proportion of revenues in each quarter; potential product performance and quality issues; the possible loss of key employees, customers, or suppliers; intellectual property risks; competition; uncertainties in contractual relationships; risks relating to company research and development, sales, marketing, and distribution plans and capabilities; reductions in research and development spending or changes in budget priorities by customers; seasonal variations in customer operations; unanticipated increases in costs or expenses; and risks associated with international operations. Information on these and additional risks and uncertainties and other information affecting Fluidigm's business and operating results is contained in its Annual Report on Form 10-K for the year ended December 31, 2019, and in its other filings with the Securities and Exchange Commission. These forward-looking statements speak only as of the date hereof. Fluidigm disclaims any obligation to update these forward-looking statements except as may be required by law.
About Fluidigm
Fluidigm (Nasdaq:FLDM) is an industry-leading biotechnology tools provider with a vision to improve life through comprehensive health insight. We focus on the most pressing needs in translational and clinical research, including cancer, immunology, and immunotherapy. Using proprietary CyTOF and microfluidics technologies, we develop, manufacture, and market multi-omic solutions to drive meaningful insights in health and disease, identify biomarkers to inform decisions, and accelerate the development of more effective therapies. Our customers are leading academic, government, pharmaceutical, biotechnology, and plant and animal research laboratories worldwide. Together with them, we strive to increase the quality of life for all. For more information, visit fluidigm.com.
Fluidigm, the Fluidigm logo, AccuLift, Biomark, CyTOF, Direct, Imaging Mass Cytometry, Immune Profiling Assay, Maxpar, and Pathsetter are trademarks and/or registered trademarks of Fluidigm Corporation in the United States and/or other countries. Fluidigm products are provided for Research Use Only. Not for use in diagnostic procedures.
Available Information **** We use our website (fluidigm.com), investor site (investors.fluidigm.com), corporate Twitter account (@fluidigm), Facebook page (facebook.com/Fluidigm), and LinkedIn page (linkedin.com/company/fluidigm-corporation) as channels of distribution of information about our products, our planned financial and other announcements, our attendance at upcoming investor and industry conferences, and other matters. Such information may be deemed material information, and we may use these channels to comply with our disclosure obligations under Regulation FD. Therefore, investors should monitor our website and our social media accounts in addition to following our press releases, SEC filings, public conference calls, and webcasts.
Contact:
Investors: Agnes Lee Vice President, Investor Relations Fluidigm Corporation 650 416 7423 agnes.lee@fluidigm.com
Media: Mark Spearman Senior Director, Corporate Communications 650 243 6621 mark.spearman@fluidigm.com
| FLUIDIGM CORPORATION | ||||||
|---|---|---|---|---|---|---|
| CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS | ||||||
| (In thousands, except per share amounts) | ||||||
| (Unaudited) | ||||||
| Three Months Ended | ||||||
| March 31, | ||||||
| 2020 | 2019 | |||||
| Revenue: | ||||||
| Product revenue | $ | 18,981 | $ | 24,827 | ||
| Service revenue | 5,186 | 5,284 | ||||
| Product and service revenue | 24,167 | 30,111 | ||||
| Grant revenue | 350 | — | ||||
| License revenue | 3,100 | — | ||||
| Total revenue | 27,617 | 30,111 | ||||
| Costs and expenses: | ||||||
| Cost of product revenue | 9,640 | 11,389 | ||||
| Cost of service revenue | 1,525 | 1,732 | ||||
| Cost of product and service revenue | 11,165 | 13,121 | ||||
| Research and development | 8,699 | 8,372 | ||||
| Selling, general and administrative | 22,695 | 22,824 | ||||
| Total costs and expenses | 42,559 | 44,317 | ||||
| Loss from operations | (14,942 | ) | (14,206 | ) | ||
| Interest expense | (900 | ) | (2,701 | ) | ||
| Loss on extinguishment of debt | — | (9,000 | ) | |||
| Other income (loss), net | (818 | ) | 484 | |||
| Loss before income taxes | (16,660 | ) | (25,423 | ) | ||
| Income tax benefit (expense) | 680 | (42 | ) | |||
| Net loss | $ | (15,980 | ) | $ | (25,465 | ) |
| Net loss per share, basic and diluted | $ | (0.23 | ) | $ | (0.44 | ) |
| Shares used in computing net loss per share, basic and diluted | 70,458 | 58,411 | ||||
| FLUIDIGM CORPORATION | ||||||
| --- | --- | --- | --- | --- | ||
| CONDENSED CONSOLIDATED BALANCE SHEETS | ||||||
| (In thousands) | ||||||
| (Unaudited) | ||||||
| March 31, 2020 | December 31, 2019 (1) | |||||
| ASSETS | ||||||
| Current assets: | ||||||
| Cash and cash equivalents (Note 2) | $ | 34,992 | $ | 21,661 | ||
| Short-term investments (Note 2) | 13,493 | 36,978 | ||||
| Accounts receivable, net | 14,410 | 18,981 | ||||
| Inventories | 16,294 | 13,884 | ||||
| Prepaid expenses and other current assets (Note 2) | 3,244 | 4,592 | ||||
| Total current assets | 82,433 | 96,096 | ||||
| Property and equipment, net | 8,143 | 8,056 | ||||
| Operating lease right-of-use assets, net | 39,499 | 4,860 | ||||
| Other non-current assets (Note 2) | 5,204 | 5,492 | ||||
| Developed technology, net | 48,612 | 46,200 | ||||
| Goodwill | 106,328 | 104,108 | ||||
| Total assets | $ | 290,219 | $ | 264,812 | ||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||
| Current liabilities: | ||||||
| Accounts payable | $ | 9,440 | $ | 6,510 | ||
| Accrued compensation and related benefits | 5,616 | 5,160 | ||||
| Operating lease liabilities, current | 1,185 | 1,833 | ||||
| Other accrued liabilities | 6,456 | 7,515 | ||||
| Deferred revenue, current portion | 12,667 | 11,803 | ||||
| Total current liabilities | 35,364 | 32,821 | ||||
| Convertible notes, net | 53,920 | 53,821 | ||||
| Deferred tax liability, net | 10,929 | 11,494 | ||||
| Operating lease liabilities, non-current | 39,611 | 4,323 | ||||
| Deferred revenue, non-current | 8,438 | 8,168 | ||||
| Other non-current liabilities | 461 | 573 | ||||
| Total liabilities | 148,723 | 111,200 | ||||
| Total stockholders' equity | 141,496 | 153,612 | ||||
| Total liabilities and stockholders' equity | $ | 290,219 | $ | 264,812 | ||
| Notes: | ||||||
| (1) Derived from audited consolidated financial statements | ||||||
| (2) Cash and cash equivalents, available for sale securities and restricted cash consist of: | ||||||
| Cash and cash equivalents | $ | 34,992 | $ | 21,661 | ||
| Short-term investments | 13,493 | 36,978 | ||||
| Restricted cash (included in prepaid and other current assets, and other non-current assets) | 1,075 | 2,075 | ||||
| Total cash and cash equivalents, available for sale securities and restricted cash | $ | 49,560 | $ | 60,714 | ||
| FLUIDIGM CORPORATION | ||||||
| --- | --- | --- | --- | --- | --- | --- |
| CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS | ||||||
| (In thousands) | ||||||
| (Unaudited) | ||||||
| Three Months Ended March 31, | ||||||
| 2020 | 2019 | |||||
| Operating activities | ||||||
| Net loss | $ | (15,980 | ) | $ | (25,465 | ) |
| Depreciation and amortization | 1,092 | 1,191 | ||||
| Stock-based compensation expense | 2,366 | 2,271 | ||||
| Amortization of developed technology | 2,968 | 2,800 | ||||
| Amortization of debt discounts, premiums and issuance costs | 140 | 2,037 | ||||
| Loss on extinguishment of debt | — | 9,000 | ||||
| Loss on disposal of property and equipment | — | 70 | ||||
| Other non-cash items | 459 | 110 | ||||
| Changes in assets and liabilities, net | 4,660 | (12,144 | ) | |||
| Net cash used in operating activities | (4,295 | ) | (20,130 | ) | ||
| Investing activities | ||||||
| Acquisition, net of cash acquired | (5,154 | ) | — | |||
| Purchases of investments | — | (9,491 | ) | |||
| Proceeds from sales and maturities of investments | 23,644 | — | ||||
| Purchases of property and equipment | (1,030 | ) | (266 | ) | ||
| Net cash provided by (used in) investing activities | 17,460 | (9,757 | ) | |||
| Financing activities | ||||||
| Payment of debt issuance costs | (357 | ) | — | |||
| Proceeds from (payments for) employee equity programs, net | (146 | ) | 147 | |||
| Net cash provided by (used in) financing activities | (503 | ) | 147 | |||
| Effect of foreign exchange rate fluctuations on cash and cash equivalents | (331 | ) | (27 | ) | ||
| Net increase (decrease) in cash, cash equivalents and restricted cash | 12,331 | (29,767 | ) | |||
| Cash, cash equivalents and restricted cash at beginning of period | 23,736 | 95,401 | ||||
| Cash, cash equivalents and restricted cash at end of period | $ | 36,067 | $ | 65,634 | ||
| Cash and cash equivalents, restricted cash and available for sale securities consist of: | ||||||
| Cash and cash equivalents | $ | 34,992 | $ | 21,661 | ||
| Short-term investments | 13,493 | 36,978 | ||||
| Restricted cash (included in prepaid and other current assets, and other non-current assets) | 1,075 | 1,075 | ||||
| Total cash and cash equivalents, available for sale securities and restricted cash | $ | 49,560 | $ | 59,714 | ||
| FLUIDIGM CORPORATION | ||||||
| --- | --- | --- | --- | --- | --- | --- |
| RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION | ||||||
| (In thousands, except per share amounts) | ||||||
| (Unaudited) | ||||||
| ITEMIZED RECONCILIATION BETWEEN GAAP AND NON-GAAP NET LOSS | ||||||
| Three Months Ended March 31, | ||||||
| 2020 | 2019 | |||||
| Net loss (GAAP) | $ | (15,980 | ) | $ | (25,465 | ) |
| Stock-based compensation expense | 2,366 | 2,271 | ||||
| Amortization of developed technology (a) | 2,968 | 2,800 | ||||
| Depreciation and amortization | 1,092 | 1,191 | ||||
| Interest expense (b) | 900 | 2,701 | ||||
| Loss on disposal of property and equipment | — | 70 | ||||
| Loss on extinguishment of debt | — | 9,000 | ||||
| Benefit from acquisition related income taxes (c) | (742 | ) | (742 | ) | ||
| Net loss (Non-GAAP) | $ | (9,396 | ) | $ | (8,174 | ) |
| Shares used in net loss per share calculation - | ||||||
| basic and diluted (GAAP and Non-GAAP) | 70,458 | 58,411 | ||||
| Net loss per share - basic and diluted (GAAP) | $ | (0.23 | ) | $ | (0.44 | ) |
| Net loss per share - basic and diluted (Non-GAAP) | $ | (0.13 | ) | $ | (0.14 | ) |
| ITEMIZED RECONCILIATION BETWEEN GAAP AND NON-GAAP PRODUCT AND SERVICE MARGIN | ||||||
| Three Months Ended March 31, | ||||||
| 2020 | 2019 | |||||
| Product and service gross profit (GAAP) | 13,002 | 16,990 | ||||
| Amortization of developed technology (a) | 2,800 | 2,800 | ||||
| Depreciation and amortization (d) | 393 | 453 | ||||
| Stock-based compensation expense (d) | 71 | 127 | ||||
| Product and service gross profit (Non-GAAP) | $ | 16,266 | $ | 20,370 | ||
| Product and service margin percentage (GAAP) | 53.8 | % | 56.4 | % | ||
| Product and service margin percentage (Non-GAAP) | 67.3 | % | 67.7 | % | ||
| ITEMIZED RECONCILIATION BETWEEN GAAP AND NON-GAAP OPERATING EXPENSES | ||||||
| Three Months Ended March 31, | ||||||
| 2020 | 2019 | |||||
| Operating expenses (GAAP) | 31,394 | 31,196 | ||||
| Stock-based compensation expense (e) | (2,295 | ) | (2,144 | ) | ||
| Depreciation and amortization (e) | (867 | ) | (738 | ) | ||
| Loss on disposal of property and equipment (e) | — | (70 | ) | |||
| Operating expenses (Non-GAAP) | $ | 28,232 | $ | 28,244 | ||
| ITEMIZED RECONCILIATION BETWEEN GAAP AND NON-GAAP LOSS FROM OPERATIONS | ||||||
| Three Months Ended March 31, | ||||||
| 2020 | 2019 | |||||
| Loss from operations (GAAP) | $ | (14,942 | ) | $ | (14,206 | ) |
| Stock-based compensation expense | 2,366 | 2,271 | ||||
| Amortization of developed technology (a) | 2,968 | 2,800 | ||||
| Depreciation and amortization (e) | 1,092 | 1,191 | ||||
| Loss on disposal of property and equipment (e) | — | 70 | ||||
| Loss from operations (Non-GAAP) | $ | (8,516 | ) | $ | (7,874 | ) |
| (a) represents amortization of developed technology in connection with the DVS acquisition | ||||||
| (b) represents interest expense, primarily on convertible debt | ||||||
| (c) represents the tax impact on the purchase of intangible assets in connection with the DVS acquisition | ||||||
| (d) represents expense associated with cost of product revenue | ||||||
| (e) represents expense associated with research and development, selling, general and administrative activities |