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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
WASHINGTON,
DC 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): August 8, 2023
InspireMD,
Inc.
(Exact
Name of Registrant as Specified in Its Charter)
Delaware
(State
or Other Jurisdiction of Incorporation)
001-35731 |
|
26-2123838 |
(Commission
File
Number) |
|
(IRS
Employer
Identification
No.) |
4
Menorat Hamaor St.
Tel
Aviv, Israel |
|
6744832 |
(Address
of Principal Executive Offices) |
|
(Zip
Code) |
(888)
776-6804
(Registrant’s
Telephone Number, Including Area Code)
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 $0.0001 per share |
|
NSPR |
|
The
Nasdaq Capital Market LLC |
Indicate
by check mark whether the registrant is an emerging growth company as defined in as defined in Rule 405 of the Securities Act of 1933
(§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
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
August 8, 2023, InspireMD, Inc. issued a press release announcing its financial and operating results and recent highlights for the three
and six months ended June 30, 2023. A copy of this press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.
In
accordance with General Instruction B.2 of Form 8-K, the information in this Current Report on Form 8-K that is furnished pursuant to
this Item 2.02 shall not be deemed to be “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as
amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, and shall not be incorporated by reference
into any registration statement or other document filed under the Securities Act of 1933, as amended, or the Exchange Act, except as
shall be expressly set forth by specific reference in such filing.
Item
9.01 Financial Statements and Exhibits.
(d)
Exhibits
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 hereunto duly authorized.
|
INSPIREMD, INC. |
|
|
|
Date:
August 8, 2023 |
By: |
/s/
Amir Kohen |
|
Name: |
Amir
Kohen |
|
Title: |
Interim
Chief Financial Officer |
Exhibit
99.1

InspireMD
Reports Second Quarter 2023 Financial Results and Provides
Business
Update
-
Completed transformational private placement for up to $113.6 million, including $42.2 million upfront –
-
Completed enrollment in the C-Guardians US IDE trial; on track to announce primary and secondary endpoints and, if successful, submit
PMA application in H2 2024 –
-
Generated Q2 2023 CGuard EPS revenue of $1.6 million, an increase of nearly 10% over Q2 2022 –
—
Management
to host investor conference call today, August 8, at 8:30am ET
—
Tel
Aviv, Israel, and Miami, FL — August 8, 2023 – InspireMD, Inc. (Nasdaq: NSPR), developer of the CGuard™ Embolic
Prevention Stent System (EPS) for treatment of carotid artery disease and prevention of stroke today announced financial and operating
results for the second quarter ended June 30, 2023.
Second
Quarter 2023 and Recent Developments:
| ● | Successfully
completed a transformational private placement of common shares, prepaid warrants and warrants
for up to $113.6 million in gross proceeds, including $42.2 million upfront and additional
proceeds of up to $71.4 million upon exercise of milestone-driven warrants. |
| ● | Completed
enrollment in the C-Guardians Investigational Device Exemption (IDE) Clinical Trial. The
Company anticipates announcing primary and secondary endpoints and, if successful, submitting
a Premarket Approval (PMA) application to FDA in the second half of 2024. |
| ● | Announced
the first-in-human cases successfully performed with its CGuard Prime CAS stent delivery
platform as part of C-Guardians trial enrollment. |
| ● | Generated
record CGuard revenue for the second quarter 2023 of $1,649,000, a 9.6 % increase over the
same period in 2022 and a 33% increase over the first quarter of 2023. |
| ● | Sold
2,804 CGuard EPS stent systems in the second quarter of 2023, as compared to 2,602 in the
second quarter of 2022, an increase of 7.8%, and compared to 2,033 in the first quarter of
2023, an increase of 38%. |
Marvin
Slosman, CEO of InspireMD, commented: “Our second quarter was marked by several transformational milestones for our business,
including the financing of up to $113.6 million that we announced in May. This capital allows us to advance our business towards multiple
value-creating milestones, including obtaining potential regulatory approval of and launching our CGuard stent system in the U.S., initiating
regulatory pathways for new advanced indications for CGuard, and developing new products, while at the same time continuing to grow our
business in approved markets outside of the United States.

“We
also announced completion of enrollment in our C-Guardians IDE trial, which includes the first ever cases performed with our CGuard Prime
CAS stent delivery platform that we also plan to include in our regulatory submissions. Importantly, enrollment was completed efficiently
in under 24 months and gives us line of sight to results and, if successful, a PMA submission in the second half of next year. In parallel,
we continue to advance critical pre-commercial activities in the U.S. with the goal of launching CGuard Prime in the first half of 2025,
if approved.
“The
ongoing shift toward an endovascular standard of care with both CAS and TCAR, highlighted by the current CMS proposed decision memo to
expand reimbursement for CAS, further validates our strategic direction. We are striving to serve all physician specialties that treat
carotid disease, both CAS and TCAR, with our best-in-class CGuard EPS implant. We believe we are optimally positioned to make the CGuard
EPS stent system the standard of care, not only in the U.S. but globally,” Mr. Slosman concluded.
Financial
Results for the Second Quarter ended June 30, 2023
For
the three months ended June 30, 2023, revenue increased by $118,000, or 7.7%, to $1,649,000, from $1,531,000 during the three months
ended June 30, 2022. This increase was predominantly driven by a 9.6% increase in sales of CGuard EPS from $1,505,000 during the three
months ended June 30, 2022, to $1,649,000 during the three months ended June 30, 2023.
For
the three months ended June 30, 2023, gross profit (revenue less cost of revenues) increased by $60,000, or 14.0%, to $491,000, from
$431,000 during the three months ended June 30, 2022. This increase in gross profit resulted from a $90,000 increase in revenues (as
mentioned above), less the associated related material and labor offset by $30,000 in miscellaneous expenses. Gross margin (gross profits
as a percentage of revenue) increased to 29.8% during the three months ended June 30, 2023, from 28.1% during the three months ended
June 30, 2022, driven by the factors mentioned above.
Total
operating expenses for the second quarter of 2023, were $5,806,000, an increase of $694,000 or 13.6% compared to $5,122,000 for the second
quarter of 2022. This increase was primarily due to an increase in compensation expenses.
Net
loss for the second quarter of 2023 totaled $5,077,000 or $0.24 per basic and diluted share, compared to a net loss of $4,636,000, or
$0.59 per basic and diluted share, for the same period in 2022.
As
of June 30, 2023, cash, cash equivalents and short-term investments and bank deposits were $47.0 million compared to $17.8 million as
of December 31, 2022. This includes the initial net funding of $37.5 million received upon closing of the transformational private placement
that was announced in May, after deducting transaction expenses.
Financial
Results for the Six Months ended June 30, 2023
For
the six months ended June 30, 2023, revenue increased by $174,000, or 6.4%, to $2,888,000, from $2,714,000 during the six months ended
June 30, 2022. This increase was predominantly driven by a 8.3% increase in sales volume of CGuard EPS from $2,666,000 during the six
months ended June 30, 2022, to $2,888,000 during the six months ended June 30, 2023.

For
the six months ended June 30, 2023, gross profit (revenue less cost of revenues) increased by 56.2%, or $311,000, to $864,000, compared
to a $553,000 for the same period in 2022. This increase in gross profit resulted from a decrease in write-offs of $181,000 and a $161,000
increase in revenues (as mentioned above) less the associated related material and labor costs. This increase was partially offset by
an increase of $31,000 in miscellaneous expenses. Gross margin (gross profits as a percentage of revenue) increased to 29.9% during the
six months ended June 30, 2023, from 20.4% during the six months ended June 30, 2022, driven by the reasons mentioned above.
Total
operating expenses for the six months ended June 30, 2023, were $10,560,000, an increase of $840,000, or 8.6% compared to $9,720,000
for the six months ended June 30, 2022. This increase was primarily due to an increase in compensation and other general and administrative
expenses.
Net
loss for the six months ended June 30, 2023 totaled $9,333,000, or $0.64 per basic and diluted share, compared to a net loss of $9,117,000,
or $1.17 per basic and diluted share, for the six months ended June 30, 2022.
Conference
Call and Webcast Details
Management
will host a conference call today, Tuesday, August 8, at 8:30 AM ET, to review financial results and provide an update on corporate developments.
Following management’s formal remarks, there will be a question-and-answer session.
Tuesday,
August 8th, at 8:30 a.m. ET
|
Domestic:
|
|
1-844-826-3035 |
|
|
International:
|
|
1-412-317-5195 |
|
|
Conference
ID: |
|
10180798 |
|
|
Call
me™ |
|
Link
here |
|
|
Webcast:
|
|
Link
here |
|
About
InspireMD, Inc.
InspireMD
seeks to utilize its proprietary MicroNet® technology to make its products the industry standard for carotid stenting by providing
outstanding acute results and durable, stroke-free, long-term outcomes. InspireMD’s common stock is quoted on the Nasdaq under
the ticker symbol NSPR.
We
routinely post information that may be important to investors on our website. For more information, please visit www.inspiremd.com.

Forward-looking
Statements
This
press release contains “forward-looking statements.” Forward-looking statements include, but are not limited to, statements
regarding InspireMD or its management team’s expectations, hopes, beliefs, intentions or strategies regarding the future. Such
statements may be preceded by the words “intends,” “may,” “will,” “plans,” “expects,”
“anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,”
“hopes,” “potential”, “scheduled” or similar words. Forward-looking statements are not guarantees
of future performance, are based on certain assumptions and are subject to various known and unknown risks and uncertainties, many of
which are beyond the company’s control, and cannot be predicted or quantified and consequently, actual results may differ materially
from those expressed or implied by such forward-looking statements. Such risks and uncertainties include, without limitation, risks and
uncertainties associated with our history of recurring losses and negative cash flows from operating activities, significant future commitments
and the uncertainty regarding the adequacy of our liquidity to pursue our complete business objectives; our need to raise additional
capital to meet our business requirements in the future and such capital raising may be costly or difficult to obtain and could dilute
out stockholders’ ownership interests; market acceptance of our products; an inability to secure and maintain regulatory approvals
for the sale of our products; negative clinical trial results or lengthy product delays in key markets; our ability to maintain compliance
with the Nasdaq listing standards; our ability to generate revenues from our products and obtain and maintain regulatory approvals for
our products; our ability to adequately protect our intellectual property; our dependence on a single manufacturing facility and our
ability to comply with stringent manufacturing quality standards and to increase production as necessary; the risk that the data collected
from our current and planned clinical trials may not be sufficient to demonstrate that our technology is an attractive alternative to
other procedures and products; intense competition in our industry, with competitors having substantially greater financial, technological,
research and development, regulatory and clinical, manufacturing, marketing and sales, distribution and personnel resources than we do;
entry of new competitors and products and potential technological obsolescence of our products; inability to carry out research, development
and commercialization plans; loss of a key customer or supplier; technical problems with our research and products and potential product
liability claims; product malfunctions; price increases for supplies and components; insufficient or inadequate reimbursement by governmental
and other third-party payers for our products; our efforts to successfully obtain and maintain intellectual property protection covering
our products, which may not be successful; adverse federal, state and local government regulation, in the United States, Europe or Israel
and other foreign jurisdictions; the fact that we conduct business in multiple foreign jurisdictions, exposing us to foreign currency
exchange rate fluctuations, logistical and communications challenges, burdens and costs of compliance with foreign laws and political
and economic instability in each jurisdiction; the escalation of hostilities in Israel, which could impair our ability to manufacture
our products; and current or future unfavorable economic and market conditions and adverse developments with respect to financial institutions
and associated liquidity risk. More detailed information about the Company and the risk factors that may affect the realization of forward-looking
statements is set forth in the Company’s filings with the Securities and Exchange Commission (SEC), including the Company’s
Annual Report on Form 10-K and its Quarterly Reports on Form 10-Q. Investors and security holders are urged to read these documents free
of charge on the SEC’s web site at http://www.sec.gov. The Company assumes no obligation to publicly update or revise its forward-looking
statements as a result of new information, future events or otherwise.
Investor
Contacts:
Craig
Shore
Chief
Financial Officer
InspireMD,
Inc.
888-776-6804
craigs@inspiremd.com
Chuck
Padala, Managing Director
LifeSci
Advisors
646-627-8390
chuck@lifesciadvisors.com
investor-relations@inspiremd.com

CONSOLIDATED STATEMENTS OF OPERATIONS (1) |
(U.S. dollars in thousands, except per share data) |
| |
| |
| |
Three months ended | | |
Six months ended | |
| |
June 30, | | |
June 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
| |
| | |
| | |
| | |
| |
Revenues | |
$ | 1,649 | | |
$ | 1,531 | | |
$ | 2,888 | | |
$ | 2,714 | |
Cost of revenues | |
| 1,158 | | |
| 1,100 | | |
| 2,024 | | |
| 2,161 | |
| |
| | | |
| | | |
| | | |
| | |
Gross Profit | |
| 491 | | |
| 431 | | |
| 864 | | |
| 553 | |
| |
| | | |
| | | |
| | | |
| | |
Operating Expenses: | |
| | | |
| | | |
| | | |
| | |
Research and development | |
| 1,993 | | |
| 2,056 | | |
| 3,836 | | |
| 3,736 | |
Selling and marketing | |
| 892 | | |
| 986 | | |
| 1,680 | | |
| 1,732 | |
General and administrative | |
| 2,921 | | |
| 2,070 | | |
| 5,044 | | |
| 4,252 | |
| |
| | | |
| | | |
| | | |
| | |
Total operating expenses | |
| 5,806 | | |
| 5,112 | | |
| 10,560 | | |
| 9,720 | |
| |
| | | |
| | | |
| | | |
| | |
Loss from operations | |
| (5,315 | ) | |
| (4,681 | ) | |
| (9,696 | ) | |
| (9,167 | ) |
| |
| | | |
| | | |
| | | |
| | |
Financial income | |
| 238 | | |
| 45 | | |
| 363 | | |
| 50 | |
| |
| | | |
| | | |
| | | |
| | |
Net Loss | |
$ | (5,077 | ) | |
$ | (4,636 | ) | |
$ | (9,333 | ) | |
$ | (9,117 | ) |
| |
| | | |
| | | |
| | | |
| | |
Net loss per share – basic and diluted | |
$ | (0.24 | ) | |
$ | (0.59 | ) | |
$ | (0.64 | ) | |
$ | (1.17 | ) |
| |
| | | |
| | | |
| | | |
| | |
Weighted average number of shares of common stock used in computing net loss per share – basic and diluted | |
| 21,074,187 | | |
| 7,807,795 | | |
| 14,619,622 | | |
| 7,806,030 | |

CONSOLIDATED BALANCE SHEETS (2) |
(U.S. dollars in thousands) |
| |
June 30, | | |
December 31, | |
| |
2023 | | |
2022 | |
| |
| | |
| |
ASSETS | |
| | |
| |
| |
| | |
| |
Current Assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 11,545 | | |
$ | 4,632 | |
Short-term bank deposits | |
| 6,631 | | |
| 13,171 | |
Marketable securities | |
| 28,817 | | |
| - | |
Accounts receivable: | |
| | | |
| | |
Trade, net | |
| 1,470 | | |
| 1,034 | |
Other | |
| 312 | | |
| 213 | |
Prepaid expenses | |
| 56 | | |
| 655 | |
Inventory | |
| 1,689 | | |
| 1,621 | |
| |
| | | |
| | |
Total current assets | |
| 50,520 | | |
| 21,326 | |
| |
| | | |
| | |
Non-current assets: | |
| | | |
| | |
Property, plant and equipment, net | |
| 873 | | |
| 917 | |
Operating lease right of use assets | |
| 1,388 | | |
| 1,554 | |
Funds in respect of employee rights upon retirement | |
| 857 | | |
| 856 | |
| |
| | | |
| | |
Total non-current assets | |
| 3,118 | | |
| 3,327 | |
| |
| | | |
| | |
Total assets | |
$ | 53,638 | | |
$ | 24,653 | |

| |
June 30, | | |
December 31, | |
| |
2023 | | |
2022 | |
LIABILITIES AND EQUITY | |
| | |
| |
| |
| | |
| |
Current liabilities: | |
| | | |
| | |
Accounts payable and accruals: | |
| | | |
| | |
Trade | |
$ | 768 | | |
$ | 659 | |
Other | |
| 4,061 | | |
| 4,411 | |
| |
| | | |
| | |
Total current liabilities | |
| 4,829 | | |
| 5,070 | |
| |
| | | |
| | |
Long-term liabilities: | |
| | | |
| | |
Operating lease liabilities | |
| 970 | | |
| 1,195 | |
Liability for employees rights upon retirement | |
| 1,026 | | |
| 995 | |
Total long-term liabilities | |
| 1,996 | | |
| 2,190 | |
| |
| | | |
| | |
Total liabilities | |
$ | 6,825 | | |
$ | 7,260 | |
| |
| | | |
| | |
Equity: | |
| | | |
| | |
Common stock, par value $0.0001 per share; 150,000,000 shares authorized at June 30, 2023 and December 31, 2022; 21,192,204 and 8,330,918 shares issued and outstanding at June 30, 2023 and December 31, 2022, respectively | |
| 2 | | |
| 1 | |
Preferred C shares, par value $0.0001 per share; 1,172,000 shares authorized at June 30, 2023 and December 31, 2022; 1,718 shares issued and outstanding at June 30, 2023 and December 31, 2022, respectively | |
| * | | |
| * | |
Additional paid-in capital | |
| 257,729 | | |
| 218,977 | |
Accumulated deficit | |
| (210,918 | ) | |
| (201,585 | ) |
| |
| | | |
| | |
Total equity | |
| 46,813 | | |
| 17,393 | |
| |
| | | |
| | |
Total liabilities and equity | |
$ | 53,638 | | |
$ | 24,653 | |
(1)
All 2023 financial information is derived from the Company’s 2023 unaudited financial statements, as disclosed in the Company’s
Quarterly Report on Form 10-Q, filed with the Securities and Exchange Commission; all 2022 financial information is derived from the
Company’s 2022 unaudited financial statements, as disclosed in the Company’s Quarterly Report on Form 10-Q, filed with the
Securities and Exchange Commission.
(2)
All June 30, 2023 financial information is derived from the Company’s 2023 unaudited financial statements, as disclosed in the
Company’s Quarterly Report on Form 10-Q, filed with the Securities and Exchange Commission. All December 31, 2022 financial information
is derived from the Company’s 2022 audited financial statements as disclosed in the Company’s Annual Report on Form 10-K,
for the twelve months ended December 31, 2022 filed with the Securities
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