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Microbot Medical (MBOT) gains new LIBERTY robotic adopters post-SIR

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Microbot Medical Inc. filed a current report describing commercial progress for its LIBERTY Endovascular Robotic System. Following the Full Market Release at the Society of Interventional Radiology annual meeting, the company reports strong interest from physicians and hospital executives and has already won multiple accounts in key sales territories.

The new accounts include two sites that previously participated in the ACCESS-PVI pivotal clinical trial, which the company highlights as validation that trial users see value in adopting LIBERTY for everyday practice. Microbot plans to further showcase LIBERTY at the Global Embolization Symposium & Technologies conference in New York in mid-May and is expanding its international commercial infrastructure, including a new Vice President of Sales for EMEA.

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Item 7.01 Regulation FD Disclosure Disclosure
Material non-public information disclosed under Regulation Fair Disclosure, often investor presentations or guidance.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Regulation FD regulatory
"Item 7.01 Regulation FD Disclosure."
Regulation FD is a rule that prevents company insiders, like executives, from sharing important information with some people before others get it. It matters because it helps ensure all investors have equal access to key news, making the stock market fairer and reducing chances of insider trading.
Full Market Release financial
"following the commencement of the Full Market Release of its LIBERTY"
A full market release is the simultaneous public distribution of material company information through official channels so all investors and market participants receive the same news at the same time. It matters because it promotes fair and orderly trading—reducing the chance that a few people trade on secret information—and can trigger immediate price moves as everyone reassesses a stock based on the newly shared facts, like broadcasting an announcement to an entire stadium at once.
LIBERTY Endovascular Robotic System medical
"developer and distributor of the innovative LIBERTY Endovascular Robotic System"
pivotal clinical trial medical
"including two accounts that participated in the Company’s ACCESS-PVI pivotal clinical trial"
A pivotal clinical trial is a late-stage medical study designed to provide the main evidence regulators use to decide whether a drug or medical device can be approved and sold; think of it as the product’s final exam. For investors, the trial’s outcome is critical because a clear pass can unlock regulatory approval, market access and future revenue, while failure can halt commercialization and materially affect a company’s valuation.
forward-looking statements regulatory
"constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act"
Forward-looking statements are predictions or plans that companies share about what they expect to happen in the future, like estimating sales or profits. They matter because they help investors understand a company's outlook, but since they are based on guesses and assumptions, they can sometimes be wrong.
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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 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): May 5, 2026

 

MICROBOT MEDICAL INC.

(Exact name of registrant as specified in its charter)

 

Delaware   000-19871   94-3078125

(State or other jurisdiction

of incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

 

175 Derby St., Bld. 27

Hingham, MA 02043

(Address of Principal Executive Offices) (Zip Code)

 

Registrant’s telephone number, including area code: (781) 875-3605

 

 

(Former Name or Former Address, if Changed Since Last Report)

 

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, $0.01 par value   MBOT   NASDAQ Capital Market

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (17 CFR §230.405) or Rule 12b-2 of the Securities Exchange Act of 1934 (17 CFR §240.12b-2).

 

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 7.01 Regulation FD Disclosure.

 

On May 5, 2026, Microbot Medical Inc. (the “Company”) issued a press release announcing that it is experiencing strong interest from physicians and hospital executives following the commencement of the Full Market Release of its LIBERTY® Endovascular Robotic System at the recent Society of Interventional Radiology (SIR) annual meeting, and has since won accounts in key sales territories, including two accounts that participated in the Company’s ACCESS-PVI pivotal clinical trial.

 

The press release, which is furnished as Exhibit 99.1 to this Current Report on Form 8-K, is incorporated herein by reference. The information in this Item 7.01 and Exhibit 99.1 is being furnished and shall not be deemed to be “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section. This report will not be deemed an admission as to the materiality of any information in this Item 7.01 or Exhibit 99.1.

 

Item 9.01. Financial Statements and Exhibits.

 

(d) Exhibits

 

Exhibit
Number
  Description
     
99.1   Press Release
104   Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

 

 

 

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 thereunto duly authorized.

 

  MICROBOT MEDICAL INC.
   
  By: /s/ Harel Gadot
  Name:  Harel Gadot
  Title: Chief Executive Officer, President and Chairman

 

Date: May 5, 2026

 

 

 

 

Exhibit 99.1

 

 

Microbot Medical®’s LIBERTY® Endovascular Robotic System is Now Adopted by Multiple Accounts Across Key Territories Including Two ACCESS-PVI Pivotal Clinical Trial Sites

 

Commercial adoption of the LIBERTY System by sites that participated in the clinical trial serves as a strong validation of the value it brings to everyday practice.

 

The Company will attend the Annual Global Embolization Symposium & Technologies (GEST), a Premier Medical Conference in New York City that attracts over 1,000 global experts across key target call points

 

HINGHAM, Mass., May 5, 2026 -- Microbot Medical Inc. (Nasdaq: MBOT), developer and distributor of the innovative LIBERTY Endovascular Robotic System, which is experiencing strong interest from physicians and hospital executives following the commencement of the Full Market Release of LIBERTY at the recent Society of Interventional Radiology (SIR) annual meeting, has since won accounts in key sales territories, including two accounts that participated in the ACCESS-PVI pivotal clinical trial.

 

The Company continues to benefit from growing commercial interest, supported by recently updated medical guidelines aimed at reducing radiation exposure and improving ergonomic challenges that have contributed to staffing challenges in interventional care. The Company expects to further raise its profile at the Annual Global Embolization Symposium & Technologies (GEST) Conference, being held in New York City from May 14-17, 2026. GEST attracts a global network of over 1,000 Interventional Radiologists (IR) and Interventional Oncologists (IO), where they meet to advance embolotherapy, learn about the latest innovative techniques, and launch the newest products.

 

With physicians attending from around the world, participation in the upcoming GEST conference represents a further step in expanding the Company’s footprint to ultimately establish a global commercial infrastructure. This effort is supported by the recent appointment of Alon Tamir as Vice President of Sales, EMEA, to lead commercialization across key international markets.

 

“We are seeing the effects of a strong tailwind post SIR and are off to a strong full market release as we have already added new accounts and are pursuing several other opportunities across existing and newly added sales territories,” commented Harel Gadot, Chairman, CEO and President. “The timing of the Annual GEST Conference is especially opportune, as it represents our first major conference featuring the LIBERTY system following last month’s full market release during SIR. With increased usability of LIBERTY, we believe peer-to-peer communications between current and future users has expanded which could drive physicians to our booth at GEST to experience LIBERTY firsthand; helping to sustain this momentum as we expand our commercial activities in the U.S. and establish the infrastructure in key international markets in the second half of the year.”

 

 

 

 

About Microbot Medical

 

Microbot Medical Inc. (NASDAQ: MBOT) is a commercial stage medical device company focused on transforming endovascular procedures through advanced robotic technology. Microbot’s LIBERTY® Endovascular Robotic System is the first single-use, remotely operated robotic solution designed for precision, efficiency and safety. Backed by a strong intellectual property portfolio and a commitment to innovation, Microbot is driving the future of endovascular care.

 

Learn more at www.microbotmedical.com and connect on LinkedIn and X.

 

Safe Harbor

 

Statements to future financial and/or operating results, future adoption of products, future growth in research, technology, clinical development, commercialization and potential opportunities for Microbot Medical Inc. and its subsidiaries, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management, constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and the Federal securities laws. Any statements that are not historical fact (including, but not limited to statements that contain words such as “contemplates,” “continues,” “could,” “forecasts,” “intends,” “may,” “might,” “possible,” “potential,” “predicts,” “projects,” “should,” “would,” “will,” “believes,” “plans,” “anticipates,” “expects,” “estimates” and similar expressions) should also be considered to be forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. Forward-looking statements involve risks and uncertainties, including, without limitation, market conditions, risks inherent in the commercialization of the LIBERTY® Endovascular Robotic System, and in the development of future versions of or applications for the system, uncertainty in the results of regulatory pathways and regulatory approvals, uncertainty resulting from political, social and geopolitical conditions, particularly any changes in personnel or processes or procedures at the FDA and announcements of tariffs on imports into the U.S., disruptions resulting from new and ongoing hostilities between Israel and the Palestinians, Iran and other neighboring countries, and maintenance of intellectual property rights. Additional information on risks facing Microbot Medical® can be found under the heading “Risk Factors” in Microbot Medical’s periodic reports filed with the Securities and Exchange Commission (SEC), which are available on the SEC’s web site at www.sec.gov. Microbot Medical® disclaims any intent or obligation to update these forward-looking statements, except as required by law.

 

Contacts:

 

IR@microbotmedical.com

Media@microbotmedical.com

 

 

 

FAQ

What did Microbot Medical (MBOT) disclose in its latest 8-K filing?

Microbot Medical reported growing commercial adoption of its LIBERTY Endovascular Robotic System and strong interest from physicians and hospital executives. The company highlighted new accounts in key territories and outlined upcoming promotional activities at the GEST conference to support continued commercialization efforts.

How is Microbot Medical (MBOT) progressing with LIBERTY system adoption?

Microbot Medical states that multiple accounts across key territories have adopted the LIBERTY Endovascular Robotic System. Two of these accounts participated in the ACCESS-PVI pivotal clinical trial, which the company presents as reinforcing LIBERTY’s perceived value in routine clinical practice among early trial users.

Why are ACCESS-PVI trial sites important to Microbot Medical (MBOT)?

Two ACCESS-PVI pivotal clinical trial sites have now become commercial customers for the LIBERTY system. Microbot Medical views this as meaningful because physicians who tested the technology in a trial setting decided to integrate it into everyday procedures, suggesting confidence in its clinical utility.

What upcoming events may support Microbot Medical’s (MBOT) LIBERTY commercialization?

Microbot Medical plans to showcase the LIBERTY system at the Global Embolization Symposium & Technologies conference in New York from May 14-17, 2026. The conference gathers over 1,000 interventional radiologists and oncologists, giving the company broad exposure to its core target users.

How is Microbot Medical (MBOT) expanding internationally for the LIBERTY system?

Microbot Medical is building a global commercial infrastructure for the LIBERTY Endovascular Robotic System. The company recently appointed a Vice President of Sales for EMEA to lead commercialization in key international markets, aligning regional leadership with its broader plan to expand beyond the U.S.

Filing Exhibits & Attachments

5 documents