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.com
HYPERFINE, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED BALANCE
SHEETS (in thousands, except share and per share amounts)
(Unaudited)
|
|
September 30, 2023 |
|
December 31, 2022 |
ASSETS |
|
|
|
|
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 |
|
|
|
|
|
|
|
|
|
|
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