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Hyperfine, Inc. Reports Third Quarter 2023 Financial Results
Source: Nasdaq GlobeNewswire / 09 Nov 2023 16:05:01 America/New_York
GUILFORD, Conn., Nov. 09, 2023 (GLOBE NEWSWIRE) -- Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking medical device company that has redefined brain imaging with the world’s first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system—the Swoop® system—today announced third quarter 2023 financial results and provided a business update.
“We remain focused on our three strategic pillars of innovation, clinical evidence, and commercialization, all while actively managing our spending, resulting in meaningful progress in the transformation of the business,” said Maria Sainz, Chief Executive Officer and President of Hyperfine, Inc. “The quarter was dominated by U.S. direct deals driving record average selling price and gross margin percentage for our business. We also received FDA clearance for our latest AI-powered software and drove strong progress on all our clinical programs, including our upcoming Alzheimer’s feasibility study.”
Third Quarter 2023 Financial Results
- Revenues for the third quarter of 2023 were $2.33 million, compared to $2.35 million in the third quarter of 2022.
- Hyperfine, Inc. sold six commercial Swoop® systems in the third quarter of 2023.
- Gross margin for the third quarter of 2023 was $1.12 million, resulting in a 48% gross margin, compared to $0.69 million in the third quarter of 2022.
- Research and development expenses for the third quarter of 2023 were $5.74 million, compared to $7.34 million in the third quarter of 2022.
- Sales, marketing, general, and administrative expenses for the third quarter of 2023 were $7.14 million, compared to $6.63 million in the third quarter of 2022.
- Net loss for the third quarter of 2023 was $10.76 million, equating to a net loss of $0.15 per share, as compared to a net loss of $13.17 million, or a net loss of $0.19 per share, for the third quarter of 2022.
Nine Months Financial Results
- Revenues for the nine months ended September 30, 2023 were $8.35 million, compared to $5.39 million in the nine months ended September 30, 2022.
- Gross margin for the nine months ended September 30, 2023 was $3.72 million, resulting in a 45% gross margin, compared to $0.61 million in the nine months ended September 30, 2022.
- Research and development expenses for the nine months ended September 30, 2023 were $16.53 million, compared to $22.94 million in the nine months ended September 30, 2022.
- Sales, marketing, general, and administrative expenses for the nine months ended September 30, 2023 were $23.68 million, compared to $37.92 million in the nine months ended September 30, 2022.
- Net loss for the nine months ended September 30, 2023 was $33.55 million, equating to a net loss of $0.47 per share, as compared to a net loss of $60.11 million, or a net loss of $0.85 per share, for the nine months ended September 30, 2022.
2023 Financial Guidance
- Management expects revenue for the full year 2023 to be $11 to $13 million.
- Management expects cash burn for the full year 2023 to be $41 to $44 million.
Conference Call
Hyperfine, Inc. will host a conference call at 1:30 p.m. PT/ 4:30 p.m. ET on Thursday, November 9, 2023, to discuss its third quarter 2023 financial results and provide a business update. Those interested in listening should register online by visiting https://investors.hyperfine.io/. and clicking on News & Events. Participants are encouraged to register more than 15 minutes before the start of the call. A live and archived audio webcast will be available through the Investors page of Hyperfine, Inc.’s corporate website at https://investors.hyperfine.io/.
About Hyperfine, Inc. and the Swoop® Portable MR Imaging® System
Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking medical technology company that has redefined brain imaging with the Swoop® system—the world’s first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of care. The Swoop® system received initial U.S. Food and Drug Administration (FDA) clearance in 2020 as a portable magnetic resonance brain imaging device for producing images that display the internal structure of the head where a full diagnostic examination is not clinically practical. When interpreted by a trained physician, these images provide information that can be useful in determining a diagnosis. The Swoop® system has been approved for brain imaging in several countries, including Canada and Australia, has UKCA certification in the United Kingdom and CE certification in the European Union, and is also available in New Zealand.
The mission of Hyperfine, Inc. is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging and data solutions. Founded by Dr. Jonathan Rothberg in a technology-based incubator called 4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists developed the Swoop® system out of a passion for redefining brain imaging methodology and how clinicians can apply accessible diagnostic imaging to patient care. Traditionally, access to costly, stationary, conventional MRI technology can be inconvenient or not available when needed most. With the portable, ultra-low-field Swoop® system, Hyperfine, Inc. is redefining the neuroimaging workflow by bringing brain imaging to the patient’s bedside. For more information, visit hyperfine.io.
Hyperfine, Swoop, and Portable MR Imaging are registered trademarks of Hyperfine, Inc.
Forward-Looking Statements
This press release includes “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Actual results of Hyperfine, Inc. (the "Company”) may differ from its expectations, estimates and projections and consequently, you should not rely on these forward-looking statements as predictions of future events. Words such as “expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,” “intend,” “plan,” “may,” “will,” “could,” “should,” “believes,” “predicts,” “potential,” “continue,” and similar expressions (or the negative versions of such words or expressions) are intended to identify such forward-looking statements. These forward-looking statements include, without limitation, expectations about the Company’s financial and operating results, the Company’s goals and commercial plans, the Company’s Alzheimer’s feasibility study, the benefits of the Company’s products and services, and the Company’s future performance and its ability to implement its strategy. These forward-looking statements involve significant risks and uncertainties that could cause the actual results to differ materially from the expected results. Most of these factors are outside of the Company’s control and are difficult to predict. Factors that may cause such differences include, but are not limited to: the success, cost and timing of the Company’s product development and commercialization activities, including the degree that the Swoop® system is accepted and used by healthcare professionals; the inability to maintain the listing of the Company’s Class A common stock on the Nasdaq Stock Market LLC; the Company’s inability to grow and manage growth profitably and retain its key employees; changes in applicable laws or regulations; the inability of the Company to raise financing in the future; the inability of the Company to obtain and maintain regulatory clearance or approval for its products, and any related restrictions and limitations of any cleared or approved product; the inability of the Company to identify, in-license or acquire additional technology; the inability of the Company to maintain its existing or future license, manufacturing, supply and distribution agreements and to obtain adequate supply of its products; the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently marketing or developing; the size and growth potential of the markets for the Company’s products and services, and its ability to serve those markets, either alone or in partnership with others; the pricing of the Company’s products and services and reimbursement for medical procedures conducted using the Company’s products and services; the Company’s inability to successfully complete and generate positive data from the ACTION PMR study and the Alzheimer’s feasibility study; the Company’s estimates regarding expenses, revenue, capital requirements and needs for additional financing; the Company’s financial performance; and other risks and uncertainties indicated from time to time in Company’s filings with the Securities and Exchange Commission, including those under “Risk Factors” therein. The Company cautions readers that the foregoing list of factors is not exclusive and that readers should not place undue reliance upon any forward-looking statements which speak only as of the date made. The Company does not undertake or accept any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements to reflect any change in its expectations or any change in events, conditions or circumstances on which any such statement is based.
Investor Contact
Marissa Bych
Gilmartin Group LLC
marissa@gilmartinir.comHYPERFINE, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands, except share and per share amounts)
(Unaudited)September 30,
2023December 31,
2022ASSETS CURRENT ASSETS: Cash and cash equivalents $ 85,424 $ 117,472 Restricted cash 548 771 Accounts receivable, less allowance of $241 and $180 as of September 30, 2023 and December 31, 2022, respectively 2,437 2,103 Unbilled receivables 682 454 Inventory 6,940 4,622 Prepaid expenses and other current assets 2,184 3,194 Due from related parties — 48 Total current assets 98,215 128,664 Property and equipment, net 3,158 3,248 Other long term assets 1,691 2,139 Total assets $ 103,064 $ 134,051 LIABILITIES AND STOCKHOLDERS’ EQUITY CURRENT LIABILITIES: Accounts payable $ 908 $ 678 Deferred grant funding 548 771 Deferred revenue 1,454 1,378 Due to related parties 48 — Accrued expenses and other current liabilities 5,253 5,976 Total current liabilities 8,211 8,803 Long term deferred revenue 1,086 1,526 Total liabilities 9,297 10,329 COMMITMENTS AND CONTINGENCIES STOCKHOLDERS' EQUITY Class A Common stock, $.0001 par value; 600,000,000 shares authorized; 56,537,946 and 55,622,488 shares issued and outstanding at September 30, 2023 and December 31, 2022, respectively 5 5 Class B Common stock, $.0001 par value; 27,000,000 shares authorized; 15,055,288 shares issued and outstanding at September 30, 2023 and December 31, 2022, respectively 2 2 Additional paid-in capital 336,798 333,199 Accumulated deficit (243,038 ) (209,484 ) Total stockholders' equity 93,767 123,722 TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY $ 103,064 $ 134,051 HYPERFINE, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENT OF OPERATIONS AND COMPREHENSIVE LOSS
(in thousands, except share and per share amounts)
(Unaudited)Three Months Ended
September 30,Nine Months Ended
September 30,2023 2022 2023 2022 Sales Device $ 1,728 $ 1,945 $ 6,670 $ 4,305 Service 602 403 1,676 1,085 Total sales 2,330 2,348 8,346 5,390 Cost of sales Device 835 1,215 3,321 3,511 Service 371 445 1,302 1,272 Total cost of sales 1,206 1,660 4,623 4,783 Gross margin 1,124 688 3,723 607 Operating Expenses: Research and development 5,739 7,338 16,531 22,937 General and administrative 4,615 3,198 16,103 26,570 Sales and marketing 2,529 3,434 7,575 11,345 Total operating expenses 12,883 13,970 40,209 60,852 Loss from operations (11,759 ) (13,282 ) (36,486 ) (60,245 ) Interest income 1,021 170 2,920 203 Other income (expense), net (19 ) (59 ) 12 (63 ) Loss before provision for income taxes (10,757 ) (13,171 ) (33,554 ) (60,105 ) Provision for income taxes — — — — Net loss and comprehensive loss $ (10,757 ) $ (13,171 ) $ (33,554 ) $ (60,105 ) Net loss per common share attributable to common stockholders, basic and diluted $ (0.15 ) $ (0.19 ) $ (0.47 ) $ (0.85 ) Weighted-average shares used to compute net loss per share attributable to common stockholders, basic and diluted 71,464,315 70,509,639 71,178,769 70,398,103 HYPERFINE, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENT OF CASH FLOWS
(in thousands)
(Unaudited)Nine Months Ended
September 30,2023 2022 Cash flows from operating activities: Net loss $ (33,554 ) $ (60,105 ) Adjustments to reconcile net loss to net cash used in operating activities: Depreciation 791 754 Stock-based compensation expense 3,453 8,859 Loss on disposal of property and equipment, net 48 — Payments received on net investment in lease 25 6 Changes in assets and liabilities: Accounts receivable, net (334 ) (2,149 ) Unbilled receivables (228 ) (1,384 ) Inventory (2,494 ) 308 Prepaid expenses and other current assets 1,010 (439 ) Due from related parties 48 14 Prepaid inventory 281 — Other long term assets 142 62 Accounts payable 229 (1,522 ) Deferred grant funding (196 ) (1,403 ) Deferred revenue (364 ) 1,098 Due to related parties 48 (1,920 ) Accrued expenses and other current liabilities (776 ) 827 Net cash used in operating activities (31,871 ) (56,994 ) Cash flows from investing activities: Purchases of property and equipment (546 ) (427 ) Net cash used in investing activities (546 ) (427 ) Cash flows from financing activities: Proceeds from exercise of stock options 146 2 Net cash provided by financing activities 146 2 Net decrease in cash and cash equivalents and restricted cash (32,271 ) (57,419 ) Cash, cash equivalents and restricted cash, beginning of period 118,243 191,160 Cash, cash equivalents and restricted cash, end of period 85,972 133,741 Reconciliation of cash, cash equivalents, and restricted cash reported in the balance sheets Cash and cash equivalents 85,424 132,482 Restricted cash 548 1,259 Total cash, cash equivalents and restricted cash $ 85,972 $ 133,741 Supplemental disclosure of noncash information: Noncash acquisition of fixed assets $ 54 $ — Write-off of notes receivable $ — $ 90