Ra Medical Systems, Inc. (NYSE American: RMED) (“Ra Medical” or
the “Company”) reports financial results for the three and nine
months ended September 30, 2022 and provides a business update.
On September 9, 2022, Ra Medical entered into an Agreement and
Plan of Merger (the “Definitive Merger Agreement”) with privately
held Catheter Precision (“Catheter”), a medical device and
technology company focused on cardiac electrophysiology. Under the
terms of the agreement, Catheter will become a wholly owned
subsidiary of Ra Medical in a stock-for-stock reverse-merger
transaction (the “Merger”). If completed, the Merger will result in
a combined publicly traded company that will focus on the cardiac
electrophysiology market, one of the most robust and growing areas
of medical devices. Medtech veteran David Jenkins, who has
extensive experience growing medical device start-ups, will serve
as Chief Executive Officer of the combined company. Before taking
the role as CEO of Catheter, Mr. Jenkins was instrumental in
operating several medical device start-ups including Transneuronix,
Inc., which was acquired by Medtronic plc (NYSE:MDT) for $267
million in July 2005, and EP MedSystems, Inc., which was acquired
by St. Jude Medical for $95.7 million in July 2008.
“We have been making good progress to meet the conditions of the
proposed merger with Catheter that, if completed, will enable our
shareholders to participate in the large and growing cardiac
electrophysiology market. We effected a reverse stock split that we
believe will cure our price deficiency under NYSE American
requirements and retain our listing. We had cash and cash
equivalents of $13.7 million as of September 30, 2022 and raised a
total of approximately $7.4 million under our At-the-Market
facility (after deducting offering fees of approximately $0.2
million), of which approximately $4.9 million was raised after
September 30, 2022. We continue to advance towards meeting the
closing conditions under the merger agreement and the listing
requirements of the NYSE American exchange, although we will still
need to raise additional funds and meet the minimum price
condition,” said Will McGuire, Ra Medical CEO. “Earlier this month,
we filed an amended preliminary proxy with the Securities and
Exchange Commission (“SEC”) for a Special Meeting of Stockholders
to vote on the proposed merger, and we plan to file the definitive
proxy once we have cleared the SEC review process. Assuming the
merger proposal passes in the anticipated timeframe and the other
conditions under the merger agreement are satisfied, we continue to
expect the transaction will be completed by the end of 2022 or
early 2023.”
Catheter’s lead product is VIVO™ (an acronym for View Into
Ventricular Onset), an FDA-cleared and CE-mark product that
utilizes non-invasive inputs to locate the origin of ventricular
arrhythmias. Using VIVO, physicians can identify patients for
invasive catheter ablation and reduce the time of the invasive
procedure. Ventricular arrhythmias include ventricular
tachyarrhythmias and premature ventricular arrhythmias, diseases
that affect millions of patients and are not well treated today.
While much growth in the electrophysiology market has been for
atrial fibrillation, Catheter believes that ventricular arrhythmias
represent a large opportunity moving forward.
Catheter also intends to pursue a second generation of Amigo®, a
robotic arm with FDA clearance and CE mark that controls catheters
from outside the procedure room. Catheter has demonstrated that
patient outcomes may be enhanced by this device. Catheter is
working toward a third product release in the first half of 2023
for a device that helps close the insertion site from percutaneous
catheters or other devices. The worldwide market for this closure
assist device is believed to exceed one million procedures per
year.
The share numbers, per share numbers and pricing information in
this release are adjusted to reflect the impact of the
one-for-fifty (1:50) reverse stock split of the Company’s Common
Stock that was effective as of October 3, 2022.
About the Transaction
The Merger is structured as a stock for stock reverse merger
whereby all of Catheter’s outstanding convertible promissory notes
and equity interests are to be exchanged for shares of Ra Medical
common stock and Catheter options will be assumed by the Company.
Catheter stakeholders are expected to own approximately 80% of the
combined company, and pre-merger Ra Medical equity holders are
expected to own approximately 20% of the combined company, on a
fully diluted basis calculated using the treasury stock method,
subject to certain adjustments provided for in the Merger Agreement
and further described in the amended preliminary proxy statement
filed on November 4, 2022, including adjustment based on the amount
of Ra Medical’s net cash at closing.
The boards of directors of both companies have approved the
Definitive Merger Agreement. The merger is currently expected to
close before the end of 2022 or during the first quarter of 2023,
subject to satisfying certain closing conditions including receipt
of shareholder approval by both companies. The Definitive Merger
Agreement follows the signing by Ra Medical and Catheter of a
non-binding summary of proposed terms on June 18, 2022, which was
publicly disclosed on July 22, 2022. Investors in Ra Medical are
encouraged to review the Definitive Merger Agreement, which
contains the definitive terms of the Merger.
The descriptions of the Merger, the Ra Medical Special Meeting
of Stockholders, Catheter, and the other transactions and matters
contemplated thereby or referenced herein do not purport to be
complete and are qualified in their entirety by reference to the
Company’s Current Report on Form 8-K filed with the SEC on
September 9, 2022, the Company’s Quarterly Report on Form 10-Q for
the period ended September 30, 2022 being filed with the SEC today,
and any prior or subsequent reports on Forms 10-K, 10-Q or 8-K
filed with the SEC from time to time and available on the SEC
website. The Company filed an amended preliminary proxy statement
with the SEC on November 4, 2022.
Management and Organization
The combined company will be led by David Jenkins as Executive
Chair and Chief Executive Officer following the Merger. Will
McGuire, Ra Medical’s CEO, and Brian Conn, Ra Medical’s interim
CFO, have agreed to remain with the Company through the closing of
the Merger.
Immediately following the closing of the Merger, the combined
company’s board of directors will consist of five directors, with
David Jenkins joining the board of directors as Executive Chair and
a to-be-determined current director of Ra Medical resigning at the
closing of the Merger.
Third Quarter Financial Highlights
There were no revenues reported for the third quarter of 2022.
Revenues for the third quarter of 2021 consisted of product sales
of $5,000 and cost of revenues of $0.2 million.
Selling, general and administrative expenses (SG&A) for the
third quarter of 2022 were $3.5 million, which included $85,000 in
stock-based compensation, compared with $4.2 million for the third
quarter of 2021, which included $78,000 in stock-based
compensation. Research and development (R&D) expenses for the
third quarter of 2022 were $0.7 million, which included negative
$11,000 in stock-based compensation, compared with $2.9 million for
the third quarter of 2021, which included $27,000 in stock-based
compensation.
During the third quarter of 2022, the Company recorded
additional restructuring and impairment charges of $0.5 million for
expenses related to an additional reduction in force, impairment of
property and equipment, inventory obsolescence charges and other
expenses due to the decision in the second quarter of 2022 to
discontinue the pivotal atherectomy clinical trial, cease
manufacturing activities, sell or dispose of property and equipment
and inventories, and expense prepaid R&D supplies. There were
no comparable charges in the prior-year period.
The loss from continuing operations for the third quarter of
2022 was $4.8 million, or $4.36 per share on 1.1 million
weighted-average shares outstanding. This compared with a loss from
continuing operations for the third quarter of 2021 of $7.4
million, or $57.64 per share on 0.1 million weighted-average shares
outstanding. Income from discontinued operations for the third
quarter of 2021 was $3.1 million. There was no comparable income in
the third quarter of 2022.
Adjusted EBITDA for the third quarter of 2022 was negative $4.1
million, compared with negative $6.9 million for the third quarter
of 2021. Adjusted EBITDA is a non-GAAP measure presented as loss
from continuing operations before depreciation and amortization
expense, interest income, interest expense, income tax expense,
stock-based compensation, gain on extinguishment of promissory
note, restructuring and impairment charges and loss (gain) on sales
and disposals of property and equipment. For additional information
regarding the non-GAAP financial measures discussed in this news
release, please see "Non-GAAP Reconciliations" below.
Nine Month Financial Highlights
Revenues for the first nine months of 2022 consisted of product
sales of $14,000, compared with product sales for the first nine
months of 2021 of $17,000.
Cost of revenues for the first nine months of 2022 was $0.2
million, compared with $1.2 million for the first nine months of
2021.
SG&A expenses for the first nine months of 2022 were $8.3
million, which included $0.3 million in stock-based compensation,
compared with $11.3 million for the first nine months of 2021,
which included $1.6 million in stock-based compensation. R&D
expenses for the first nine months of 2022 were $6.2 million, which
included $57,000 in stock-based compensation, compared with $8.5
million for the first nine months of 2021, which included $0.3
million in stock-based compensation.
For the nine months ended September 30, 2022, the Company
recorded restructuring and impairment charges of $4.1 million due
to the decision to discontinue the pivotal atherectomy clinical
trial, cease manufacturing activities, sell or dispose of property
and equipment and inventories, and expense prepaid R&D
supplies. There were no comparable charges in the prior-year
period.
The loss from continuing operations for the first nine months of
2022 was $18.7 million, or $28.00 per share on $0.7 million
weighted-average shares outstanding, compared with a loss from
continuing operations for the first nine months of 2021 of $19.0
million, or $210.82 per share on 90,000 weighted-average shares
outstanding. Income from discontinued operations for the third
quarter of 2021 was $2.2 million
Adjusted EBITDA for the first nine months of 2022 was negative
$13.9 million, compared with negative $18.6 million for the first
nine months of 2021.
Ra Medical reported cash and cash equivalents of $13.7 million
as of September 30, 2022.
Non-GAAP Financial Measures
Ra Medical has presented certain financial information in
accordance with U.S. GAAP and also on a non-GAAP basis for the
three and nine month periods ended September 30, 2022 and 2021.
EBITDA and Adjusted EBITDA are performance measures that provide
supplemental information management believes is useful to analysts
and investors to evaluate Ra Medical’s ongoing results of
operations, when considered alongside other GAAP measures. These
measures are intended to aid investors in better understanding Ra
Medical’s current financial performance and prospects for the
future as seen through management. 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. Management believes that these
non-GAAP financial measures facilitate comparisons with Ra
Medical’s historical results and with the results of peer companies
who present similar measures (although other companies may define
non-GAAP measures differently than we define them, even when
similar terms are used to identify such measures). 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. Ra Medical
encourages investors to carefully consider its results under U.S.
GAAP, as well as its supplemental non-GAAP information and the
reconciliation between these presentations, to more fully
understand its business. Reconciliations between U.S. GAAP and
non-GAAP operating results are presented in the accompanying tables
of this news release.
Investors are encouraged to review the related U.S. GAAP
financial measures and the reconciliation of these non-GAAP
financial measures to their most directly comparable GAAP financial
measures, and not to rely on any single financial measure to
evaluate our business. Ra Medical defines EBITDA as our GAAP loss
from continuing operations as adjusted to exclude depreciation and
amortization, interest income, interest expense and income tax
expense. Ra Medical defines Adjusted EBITDA as EBITDA adjusted to
exclude stock-based compensation, gain on extinguishment of
promissory note, restructuring and impairment charges and loss
(gain) on sales and disposals of property and equipment.
About Ra Medical Systems
Ra Medical Systems, Inc. is a medical device company that owns
intellectual property related to an advanced excimer laser-based
platform for use in the treatment of vascular immune-mediated
inflammatory diseases. Its excimer laser and single-use catheter
system, together referred to as the DABRA Excimer Laser System, is
used as a tool in the treatment of peripheral artery disease.
Cautionary Note Regarding Forward Looking Statements
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of
1995. Forward-looking statements generally relate to future events
or Ra Medical’s future financial or operating performance. In some
cases, you can identify forward-looking statements because they
contain words such as “may,” “will,” “should,” “expects,” “plans,”
“anticipates,” “could,” “intends,” “target,” “projects,”
“contemplates,” “believes,” “estimates,” “predicts,” “potential” or
“continue” or the negative of these words or other similar terms or
expressions that concern Ra Medical’s future expectations,
strategy, plans or intentions. Forward-looking statements in this
press release include, but are not limited to, statements
concerning the proposed Merger with Catheter, Ra Medical’s future
financial performance and Ra Medical’s ability to conserve capital
and maximize any strategic opportunity. Ra Medical’s expectations
and beliefs regarding these matters may not materialize, and actual
results in future periods are subject to risks and uncertainties
that could cause actual results to differ materially from those
projected or implied by such forward-looking statements. Factors
that may cause actual results to differ materially from current
expectations include, but are not limited to: (i) the risk that the
proposed Merger may not be completed in a timely manner or at all,
which may adversely affect the price of the Company’s securities;
(ii) the outcome of any legal proceedings that may be instituted
against the Company, Catheter, the combined company following the
Merger, if consummated, or others following an announcement of the
merger agreement, if entered into, relating to the proposed Merger,
any ancillary agreements contemplated thereby and the transactions
contemplated thereby; (iii) the inability to issue to obtain any
necessary stockholder approvals for the Merger, any securities
issued in connection therewith, or any transactions contemplated
thereby; (iv) the Company’s inability to satisfy or have waived the
conditions precedent to the closing of the Merger, including
certain minimum per share trading prices of Ra Medical’s common
stock, which are not currently satisfied; (v) changes to the
structure of the proposed Merger that may be required or
appropriate as a result of applicable laws or regulations or as a
condition to obtaining regulatory approval of the proposed Merger;
(vi) the ability to meet stock exchange listing standards following
the consummation of the proposed Merger, if effected; (vii) the
risk that the proposed Merger transaction disrupts current plans
and operations of the Company or diverts management’s attention
from the Company’s ongoing business operations and potential
difficulties in the Company’s operations as a result of the
announcement and consummation of the proposed Merger; (viii) the
ability to recognize the anticipated benefits of the proposed
Merger, if consummated; (ix) costs related to the proposed Merger,
if consummated; (x) changes in applicable laws or regulations; (xi)
the possibility that the Company or the combined company following
the Merger, if consummated, may be adversely affected by other
economic, business, regulatory, and/or competitive factors; (xii)
the combined company’s estimates following the Merger, if
consummated, of expenses and profitability; (xiii) the evolution of
the markets in which the combined company following the Merger, if
consummated, would compete; (xiv) the ability of the Company or the
combined company following the Merger, if consummated, to implement
its strategic initiatives and continue to innovate its existing
products; (xv) the ability of the combined company following the
Merger, if consummated, to defend its intellectual property and
satisfy regulatory requirements; (xvi) the ability of the Company
or the combined company following the Merger, if consummated, to
issue equity or equity-linked securities in connection with the
proposed Merger or in the future; (xvi) the impact of the COVID-19
pandemic on the Company’s or the combined company’s business
following the Merger, if consummated; and (xvii) other risks and
uncertainties set forth in the section entitled “Risk Factors” and
“Cautionary Note Regarding Forward-Looking Statements” in the
Company’s prospectus, dated February 4, 2022 and prospectus
supplement dated July 22, 2022 relating to its public offering of
units and other documents filed and to be filed by the Company with
the SEC, and in the Company’s Current Report on Form 8-K filed on
July 22, 2022, and other information affecting Ra Medical’s
business and operating results is contained in Ra Medical’s
Quarterly Report on Form 10-Q for the quarter ended June 30, 2022
and in its other filings with the Securities and Exchange
Commission, including the amended preliminary proxy statement filed
with the Securities and Exchange Commission on November 4, 2022.
Additional information is also set forth in Ra Medical’s Annual
Report on Form 10-K for the year ended December 31, 2021 filed with
the Securities and Exchange Commission on March 24, 2022, and as
amended on July 13, 2022. These filings identify and address other
important risks and uncertainties that could cause actual events
and results to differ materially from those contained in the
forward-looking statements.
Readers are cautioned not to put undue reliance on
forward-looking statements, and the Company and Catheter assume no
obligation and do not intend to update or revise these
forward-looking statements, whether as a result of new information,
future events, or otherwise. Neither the Company nor Catheter gives
any assurance that either the Company or Catheter will achieve its
expectations. The inclusion of any statement in this communication
does not constitute an admission by the Company or Catheter or any
other person that the events or circumstances described in such
statement are material.
Ra Medical investors and others should note that we announce
material information to the public about the company through a
variety of means, including our website (www.ramed.com), our
investor relations website (https://ir.ramed.com/), press releases,
SEC filings and public conference calls in order to achieve broad,
non-exclusionary distribution of information to the public and to
comply with our disclosure obligations under Regulation FD. We
encourage our investors and others to monitor and review the
information we make public in these locations as such information
could be deemed to be material information. Please note that this
list may be updated from time to time.
Disclaimer
This press release relates to a proposed business combination
between the Company and Catheter. This document does not constitute
an offer to sell or exchange, or the solicitation of an offer to
buy or exchange, any securities, nor shall there be any sale of
securities in any jurisdiction in which such offer, sale or
exchange would be unlawful prior to registration or qualification
under the securities laws of any such jurisdiction.
RA MEDICAL SYSTEMS,
INC.
Condensed Balance
Sheets
(in thousands, except par value
data)
(Unaudited)
September 30,
2022
December 31,
2021
ASSETS
Current Assets
Cash and cash equivalents
$
13,657
$
15,045
Accounts receivable, net
—
21
Inventories
—
986
Prepaid expenses and other current
assets
1,885
1,037
Total current assets
15,542
17,089
Property and equipment, net
—
1,809
Operating lease right-of-use assets
1,893
2,110
Other long-term assets
36
36
TOTAL ASSETS
$
17,471
$
21,044
LIABILITIES AND STOCKHOLDERS’
EQUITY
Current Liabilities
Accounts payable
$
460
$
988
Accrued expenses
2,447
4,119
Current portion of operating lease
liability
308
283
Total current liabilities
3,215
5,390
Operating lease liability
1,746
1,981
Total liabilities
4,961
7,371
Commitments and contingencies
Stockholders’ Equity
Preferred stock, $0.0001 par value; 10,000
shares authorized; no shares issued
—
—
Common stock, $0.0001 par value; 300,000
shares authorized; 1,423 and 140 shares issued and outstanding as
of September 30, 2022 and December 31, 2021, respectively
—
—
Additional paid-in capital
209,488
191,945
Accumulated deficit
(196,978
)
(178,272
)
Total stockholders’ equity
12,510
13,673
TOTAL LIABILITIES AND STOCKHOLDERS’
EQUITY
$
17,471
$
21,044
RA MEDICAL SYSTEMS,
INC.
Condensed Statements of
Operations
(in thousands, except per share
data)
(Unaudited)
Three Months Ended September
30,
Nine Months Ended September
30,
2022
2021
2022
2021
Revenues
Product sales
$
—
$
5
$
14
$
17
Cost of revenues
Product sales
—
68
42
676
Service and other
—
178
119
537
Total cost of revenues
—
246
161
1,213
Gross loss
—
(241
)
(147
)
(1,196
)
Operating expenses
Selling, general and administrative
3,514
4,211
8,292
11,285
Research and development
727
2,942
6,238
8,521
Restructuring and impairment
542
—
4,069
—
Total operating expenses
4,783
7,153
18,599
19,806
Operating loss
(4,783
)
(7,394
)
(18,746
)
(21,002
)
Other income, net
20
16
40
2,028
Loss from continuing operations before
income taxes
(4,763
)
(7,378
)
(18,706
)
(18,974
)
Income taxes
—
—
—
—
Loss from continuing operations
(4,763
)
(7,378
)
(18,706
)
(18,974
)
Discontinued operations
Income from discontinued operations before
income taxes
—
3,080
—
2,191
Income taxes
—
—
—
—
Income from discontinued
operations
—
3,080
—
2,191
Net loss
$
(4,763
)
$
(4,298
)
$
(18,706
)
$
(16,783
)
Net (loss) income per share, basic and
diluted
Continuing operations
$
(4.36
)
$
(57.64
)
$
(28.00
)
$
(210.82
)
Discontinued operations
—
24.06
—
24.34
Total net loss per share, basic and
diluted
$
(4.36
)
$
(33.58
)
$
(28.00
)
$
(186.48
)
Weighted average number of shares used in
computing net (loss) income per share, basic and diluted
1,092
128
668
90
RA MEDICAL SYSTEMS,
INC.
Non-GAAP
Reconciliations
(Unaudited)
(in thousands)
Three Months Ended September
30,
Nine Months Ended September
30,
Statements of Operations Data:
2022
2021
2022
2021
Loss from continuing operations
$
(4,763
)
$
(7,378
)
$
(18,706
)
$
(18,974
)
Depreciation and amortization
74
319
396
974
Interest income
(24
)
—
(41
)
(2
)
Interest expense
—
—
—
12
EBITDA
(4,713
)
(7,059
)
(18,351
)
(17,990
)
Stock-based compensation
80
110
365
1,887
Restructuring and impairment
542
—
4,069
—
Loss (gain) on sales and disposals of
property and equipment
—
4
44
(489
)
Gain on extinguishment of promissory
note
—
—
—
(2,023
)
Adjusted EBITDA
$
(4,091
)
$
(6,945
)
$
(13,873
)
$
(18,615
)
View source
version on businesswire.com: https://www.businesswire.com/news/home/20221114006095/en/
LHA Investor Relations Jody Cain 310-691-7100 jcain@lhai.com
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