Helius Medical Technologies, Inc. (Nasdaq:HSDT) (“Helius” or the
“Company”), a neurotech company focused on delivering a novel
therapeutic neuromodulation approach for balance and gait deficits,
today announced results for the quarter ended September 30, 2023.
Third Quarter and Recent Business Updates
- Q3 2023 revenue
of $143 thousand, compared to $196 thousand in Q3 2022, the
decrease due to the expiration of the Patient Therapy Access
Program (“PTAP”) on June 30, 2023.
- Operating cash
burn of $2.5 million in Q3 2023, a decrease of $1.4 million
compared to Q3 2022, reflecting continued focus on cash
management.
- Ended the
quarter with $7.0 million of cash, cash equivalents, and proceeds
receivable from warrant exercises, extending the Company’s cash
runway into Q2 2024.
- Received
universal product code (“UPC”) numbers from Wolters Kluwer Health –
Medi-Span® (“Medi-Span”) for the Portable Neuromodulation
Stimulator (“PoNS®”) system and mouthpiece. Together with the
previously announced Durable Medical Equipment, Prosthetics,
Orthotics and Supplies (“DMEPOS”) accreditation, the UPC numbers
allow for dual paths of reimbursement.
- Received a
letter of intent (“LOI”) from the Québec Ministry of Health and
Social Services (“MSSS”) for the purchase of up to 30 PoNS systems
across multiple sites to be used to evaluate the benefit of PoNS
TherapyTM and determine reimbursement opportunities for stroke
patients.
- Received an
order for 10 PoNS Systems from the School of Rehabilitation at the
Université de Montréal (“UdeM”) to be used to evaluate the benefit
and health economic value of PoNS Therapy in the treatment of
stroke patients.
- Added sixth
Center of Excellence to the PoNS Therapeutic Experience Program
(“PoNSTEP”), a multi-center, company-sponsored, open label
observational interventional trial designed to evaluate the impact
of adherence to PoNS Therapy in patients with multiple sclerosis
(“MS”).
- Announced the
release of a white paper published by Pacific Blue Cross (“PBC”)
and HealthTech Connex (“HTC”) demonstrating that PoNS TherapyTM can
drastically decrease disability and improve the likelihood of
returning to work for patients suffering from traumatic brain
injury (“TBI”).
“We are pleased with the tremendous progress we
made in the third quarter and recent weeks,” said Dane Andreeff,
President and Chief Executive Officer of Helius. “We began the
third quarter with the successful conclusion of our Patient Therapy
Access Program, which expired on June 30. Through PTAP, we sold
PoNS to qualifying patients at a significant discount, thereby
reducing a major barrier to access while allowing us to add to our
ongoing MS patient registry. The registry collects important health
economic evidence to establish the value of PoNS on key clinical
and therapeutic outcomes, which is critical for third party
reimbursement. In September, we opened a second path toward
reimbursement in the U.S. by receiving UPC numbers for both the
PoNS system and mouthpiece and having the codes listed in the
Medi-Span database, as we also continue to pursue HCPCS codes for
reimbursement under our DMEPOS accreditation. As a result, we are
now in the position to begin negotiating with payers using the UPC
codes specific to the PoNS systems and mouthpieces with the listed
prices of $25,700 and $7,900, respectively.
We also developed relationships with two
important Canadian Healthcare providers, receiving an order for ten
PoNS systems from the School of Rehabilitation at the Université de
Montréal as well as a letter of intent from the Québec Ministry of
Health and Social Services to purchase thirty PoNS systems to treat
gait and/or balance deficit in stroke patients. We believe that
evidence from the treatment outcome will support the health
economic benefit and cost effectiveness of incorporating PoNS
Therapy as a first line treatment for stroke patients. Furthermore,
this evidence should provide a valuable benchmark for other
Canadian healthcare providers and private payers as they evaluate
reimbursement of PoNS Therapy. The data from these clinical
application trials will also provide supporting evidence of PoNS
Therapy’s therapeutic benefit that can strengthen the
registrational program for stroke currently ongoing in the
U.S.”
Andreeff continued, “Finally, we were thrilled
by the study results from the white paper recently published by
Pacific Blue Cross and HealthTech Connex demonstrating that PoNS
Therapy can drastically decrease disability in 89% of patients
suffering from long-term disability due to chronic TBI and promote
a sustainable return to work outcome for approximately 50% of these
patients. We believe that these findings will significantly
strengthen our reimbursement efforts with Canadian insurance
companies and healthcare providers while highlighting the health
economic benefit and cost effectiveness of PoNS Therapy as we
negotiate coverage with U.S. payers.”
“With what we’ve set in motion during 2023, and
a cash runway that will take us into the second quarter of next
year, we are excited about the road ahead, and the chance to help
more people with MS, TBI, and stroke who suffer from balance and
gait impairment,” concluded Andreeff.
Third Quarter 2023 Financial
Results
Total revenue for the third quarter of 2023 was
$143 thousand, a decrease of $53 thousand compared to $196 thousand
in the third quarter of 2022, primarily attributable to decreased
unit sales of PoNS systems in the U.S. following the termination of
the PTAP on June 30, 2023, partially offset by increased net
product sales in Canada.
Cost of revenue increased to $187 thousand for
the three months ended September 30, 2023, compared to $101
thousand for the comparable period in 2022, due to fixed overhead
costs, which are primarily comprised of salaries and benefits of
employees involved in management of the supply chain and certain
production costs.
Selling, general and administrative expenses for
the third quarter of 2023 were $2.2 million, a decrease of $1.2
million compared to $3.4 million in the third quarter of 2022,
primarily the result of a decrease in performance-based stock-based
compensation.
Research and development expenses for the third
quarter of 2023 decreased slightly to $722 thousand, compared to
$751 thousand in the third quarter of 2022.
Total operating expenses for the third quarter
of 2023 decreased to $3.1 million, compared to $4.9 million in the
third quarter of 2022.
Operating loss for the third quarter of 2023
decreased $1.7 million to a loss of $3.2 million, compared to an
operating loss of $4.9 million in the third quarter of 2022.
Net loss was $3.7 million for the third quarter
of 2023, compared to a net loss of $1.0 million in the
corresponding prior year period. The basic and diluted net loss per
share for the third quarter was $5.49 per share, compared to a net
loss of $2.90 per share for the third quarter of 2022.
Cash and Liquidity
Cash used in operating activities for the three
months ended September 30, 2023 was $2.5 million, a decrease of
$1.4 million compared to the third quarter of 2022, reflecting the
results of our continued focus on managing cash burn.
As of September 30, 2023, the Company had cash
of $6.6 million, compared to $14.5 million as of December 31, 2022.
The Company also had $0.4 million in proceeds receivable from
warrant exercises as of September 30, 2023, and now estimates its
cash runway extends into the second quarter of 2024.
The Company had no debt outstanding as of
September 30, 2023.
Conference Call
As previously announced, management will host a
conference call as follows:
Date: |
Thursday, November 9, 2023 |
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Time: |
4:30 p.m. Eastern Time |
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Toll free: |
800-225-9448 |
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International: |
203-518-9708 |
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Conference ID: |
HSDTQ323 |
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Webcast: |
Click Here |
The webcast will be archived under the Newsroom
section of the Company’s investor relations website.
About Helius Medical Technologies,
Inc.
Helius Medical Technologies is a leading
neurotech company in the medical device field focused on neurologic
deficits using orally applied technology platform that amplifies
the brain’s ability to engage physiologic compensatory mechanisms
and promote neuroplasticity, improving the lives of people dealing
with neurologic diseases. The Company’s first commercial product is
the Portable Neuromodulation Stimulator. For more information about
the PoNS® or Helius Medical Technologies, visit
www.heliusmedical.com.
About the PoNS Device and PoNS
Therapy
The Portable Neuromodulation Stimulator (“PoNS”)
is an innovative, non-implantable, orally applied therapy that
delivers neurostimulation through a mouthpiece connected to a
controller and it’s used, primarily at home, with physical
rehabilitation exercise, to improve balance and gait. The PoNS
device, which delivers mild electrical impulses to the tongue, is
indicated for use in the United States as a short-term treatment of
gait deficit due to mild-to-moderate symptoms from multiple
sclerosis (“MS”) and is to be used as an adjunct to a supervised
therapeutic exercise program in patients 22 years of age and over
by prescription only.
PoNS has shown effectiveness in treating gait or
balance and a significant reduction in the risk of falling in
stroke patients in Canada, where it received authorization for sale
in three indications: (i) for use as a short-term treatment (14
weeks) of gait deficit due to mild and moderate symptoms from
stroke and is to be used in conjunction with physical therapy; (ii)
for use as a short-term treatment (14 weeks) of chronic balance
deficit due to mild-to-moderate traumatic brain injury (“mmTBI”)
and is to be used in conjunction with physical therapy; and (iii)
for use as a short-term treatment (14 weeks) of gait deficit due to
mild and moderate symptoms from MS and is to be used in conjunction
with physical therapy. PoNS is also authorized for sale in
Australia for short term use by healthcare professionals as an
adjunct to a therapeutic exercise program to improve balance and
gait. For more information visit www.ponstherapy.com.
Cautionary Disclaimer
Statement
Certain statements in this news release are not
based on historical facts and constitute forward-looking statements
or forward-looking information within the meaning of the U.S.
Private Securities Litigation Reform Act of 1995 and Canadian
securities laws. All statements other than statements of historical
fact included in this news release are forward-looking statements
that involve risks and uncertainties. Forward-looking statements
are often identified by terms such as “believe,” “expect,”
“continue,” “will,” “goal,” “aim” and similar expressions. Such
forward-looking statements include, among others, statements
regarding the Company’s expected results from business and
financial performance in 2023, the sufficiency of the Company’s
future cash position, the development, commercialization and
success of the Company’s PoNS device and related treatment, future
decisions and approvals from applicable regulatory entities in the
U.S. and Canada, and the Company’s strategic operating plans.
There can be no assurance that such statements
will prove to be accurate and actual results and future events
could differ materially from those expressed or implied by such
statements. Important factors that could cause actual results to
differ materially from the Company’s expectations include
uncertainties associated with the Company’s capital requirements to
achieve its business objectives, disruptions in the banking system
and financial markets, lingering impacts of the COVID-19 pandemic,
the effect of macroeconomic conditions and the Company’s ability to
access capital markets, the Company’s ability to train physical
therapists in the supervision of the use of the PoNS Treatment, the
Company’s ability to secure contracts with rehabilitation clinics,
the Company’s ability to obtain national Medicare coverage and to
obtain a reimbursement code so that the PoNS device is covered by
Medicare and Medicaid, the Company’s ability to build internal
commercial infrastructure, secure state distribution licenses,
build a commercial team and build relationships with Key Opinion
Leaders, neurology experts and neurorehabilitation centers, market
awareness of the PoNS device, availability of funds, manufacturing,
labor shortage and supply chain risks, disruptions in the
manufacturing process of the PoNS device due to the transition to a
new manufacturer, the Company’s ability to maintain and enforce our
intellectual property rights, clinical trials and the clinical
development process, the product development process, the
regulatory submission review and approval process, the Company’s
operating costs and use of cash, and our ability to achieve
significant revenues, ongoing government regulation, and other
risks detailed from time to time in the “Risk Factors” section of
the Company’s Annual Report on Form 10-K for the year ended
December 31, 2022, and its other filings with the United States
Securities and Exchange Commission and the Canadian securities
regulators, which can be obtained from either at www.sec.gov or
www.sedar.com.
The reader is cautioned not to place undue
reliance on any forward-looking statement. The forward-looking
statements contained in this news release are made as of the date
of this news release and the Company assumes no obligation to
update any forward-looking statement or to update the reasons why
actual results could differ from such statements except to the
extent required by law.
Investor Relations Contact
Lisa M. Wilson, In-Site Communications, Inc.T:
212-452-2793E: lwilson@insitecony.com
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Helius Medical Technologies, Inc. |
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Unaudited Condensed Consolidated Statements of
Operations |
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(in thousands, except share and per share data) |
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Three Months Ended |
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Nine Months Ended |
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September 30, |
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September 30, |
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2023 |
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2022 |
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2023 |
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2022 |
Revenue |
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|
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Product sales, net |
$ |
132 |
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|
$ |
195 |
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|
$ |
482 |
|
|
$ |
497 |
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Other revenue |
|
11 |
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|
|
1 |
|
|
|
28 |
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|
|
8 |
|
Total revenue |
|
143 |
|
|
|
196 |
|
|
|
510 |
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|
|
505 |
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Cost of revenue |
|
187 |
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|
|
101 |
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|
|
493 |
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|
|
313 |
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Gross profit (loss) |
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(44 |
) |
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|
95 |
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|
17 |
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|
192 |
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Operating expenses |
|
|
|
|
|
|
|
|
|
|
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Selling, general and administrative expenses |
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2,196 |
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|
|
3,393 |
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7,639 |
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|
8,673 |
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Research and development expenses |
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722 |
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|
751 |
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2,292 |
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|
3,468 |
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Amortization expense |
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32 |
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|
|
47 |
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|
|
109 |
|
|
|
141 |
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Goodwill and fixed asset impairment |
|
159 |
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|
|
757 |
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|
|
159 |
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|
|
757 |
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Total operating expenses |
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3,109 |
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|
|
4,948 |
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|
|
10,199 |
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|
|
13,039 |
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Loss from operations |
|
(3,153 |
) |
|
|
(4,853 |
) |
|
|
(10,182 |
) |
|
|
(12,847 |
) |
Nonoperating income (expense) |
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|
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Interest income (expense), net |
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68 |
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|
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(919 |
) |
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|
257 |
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|
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(919 |
) |
Change in fair value of derivative liability |
|
(393 |
) |
|
|
5,489 |
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|
|
2,051 |
|
|
|
5,489 |
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Foreign exchange (loss) gain |
|
(192 |
) |
|
|
(747 |
) |
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|
62 |
|
|
|
(910 |
) |
Other income (expense), net |
|
7 |
|
|
|
— |
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|
|
7 |
|
|
|
1 |
|
Nonoperating income (expense), net |
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(510 |
) |
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|
3,823 |
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|
|
2,377 |
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|
|
3,661 |
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Loss before provision for income taxes |
|
(3,663 |
) |
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|
(1,030 |
) |
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|
(7,805 |
) |
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|
(9,186 |
) |
Provision for income taxes |
|
— |
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|
|
— |
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|
— |
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|
— |
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Net loss |
$ |
(3,663 |
) |
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$ |
(1,030 |
) |
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$ |
(7,805 |
) |
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$ |
(9,186 |
) |
Loss per share |
|
|
|
|
|
|
|
|
|
|
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Basic |
$ |
(5.49 |
) |
|
$ |
(2.90 |
) |
|
$ |
(13.60 |
) |
|
$ |
(53.77 |
) |
Diluted |
$ |
(5.49 |
) |
|
$ |
(2.90 |
) |
|
$ |
(13.60 |
) |
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$ |
(53.77 |
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Weighted average number of common shares
outstanding |
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Basic |
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667,809 |
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355,754 |
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573,950 |
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|
170,823 |
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Diluted |
|
667,809 |
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|
355,754 |
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|
|
573,950 |
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|
|
170,823 |
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|
|
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Helius Medical Technologies, Inc. |
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Unaudited Condensed Consolidated Balance
Sheets |
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(in thousands, except share and per share data) |
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September 30, 2023 |
|
December 31, 2022 |
ASSETS |
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Current assets |
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Cash and cash equivalents |
$ |
6,596 |
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$ |
14,549 |
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Accounts receivable, net |
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94 |
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71 |
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Other receivables |
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472 |
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272 |
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Inventory, net |
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521 |
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589 |
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Prepaid expenses and other current assets |
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893 |
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|
1,216 |
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Total current assets |
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8,576 |
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16,697 |
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Property and equipment, net |
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182 |
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347 |
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Intangible assets, net |
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31 |
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|
140 |
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Operating lease right-of-use asset, net |
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65 |
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|
103 |
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Total assets |
$ |
8,854 |
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$ |
17,287 |
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LIABILITIES AND STOCKHOLDERS’ EQUITY |
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Current liabilities |
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Accounts payable |
$ |
497 |
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$ |
627 |
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Accrued and other current liabilities |
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849 |
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|
1,280 |
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Current portion of operating lease liabilities |
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47 |
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|
54 |
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Current portion of deferred revenue |
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42 |
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|
27 |
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Total current liabilities |
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1,435 |
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|
1,988 |
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Operating lease liabilities, net of current portion |
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23 |
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|
56 |
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Deferred revenue, net of current portion |
|
136 |
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|
175 |
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Derivative liability |
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4,239 |
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|
6,917 |
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Total liabilities |
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5,833 |
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|
9,136 |
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STOCKHOLDERS’ EQUITY |
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Class A common stock, $0.001 par value; 150,000,000 shares
authorized; 687,799 and 563,974 shares issued and outstanding as of
September 30, 2023 and December 31, 2022,
respectively |
|
1 |
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|
|
1 |
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Additional paid-in capital |
|
162,391 |
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|
159,645 |
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Accumulated deficit |
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(158,912 |
) |
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|
(151,107 |
) |
Accumulated other comprehensive loss |
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(459 |
) |
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|
(388 |
) |
Total stockholders' equity |
|
3,021 |
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|
|
8,151 |
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Total liabilities and stockholders' equity |
$ |
8,854 |
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|
$ |
17,287 |
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