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Microbot Medical (MBOT) spotlights LIBERTY robot as AMA backs radiation safety

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

Rhea-AI Filing Summary

Microbot Medical Inc. filed a current report describing a press release about its LIBERTY® Endovascular Robotic System and recent policy from the American Medical Association on occupational radiation exposure. The AMA adopted a policy in late 2025 to strengthen protections for health care professionals and trainees exposed to ionizing radiation.

Microbot emphasizes that LIBERTY is remotely operated and, in the ACCESS-PVI Study, use of the system showed a 92% relative reduction in radiation exposure. The company began a Limited Market Release of LIBERTY in late 2025 and plans a Full Market Release at the Society of Interventional Radiology conference in April 2026.

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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): March 4, 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 March 4, 2026, Microbot Medical Inc. (the “Company”) issued a press release announcing that it commends the American Medical Association’s efforts to protect health care professionals from ionizing radiation.

 

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: March 4, 2026

 

 

 

 

Exhibit 99.1

 

 

Microbot Medical® Aligns with Recently Adopted Policy of the Largest U.S.-Based Medical Association to Expand Protection for Healthcare Professionals from Ionizing Radiation

 

LIBERTY® Endovascular Robotic System’s Capability to Reduce Radiation Exposure Appeals to Hospitals and Healthcare Providers

 

HINGHAM, Mass., March 4, 2026 -- Microbot Medical Inc. (Nasdaq: MBOT), developer and distributor of the innovative LIBERTY® Endovascular Robotic System, commends the American Medical Association’s (AMA) expanding efforts to protect health care professionals from ionizing radiation. In late 2025, the AMA adopted a new policy to strengthen protections for health care professionals and trainees who may face occupational radiation exposure. The policy emphasizes the importance of continued research into the health effects of cumulative exposure to ionizing radiation, the effectiveness of Personal Protection Equipment (PPE), and education and training to minimize occupational risk to physicians and to their patients.

 

Microbot believes that this guidance underscores the growing need for solutions that enhance safety in interventional procedures, creating meaningful opportunities for technologies like LIBERTY. The LIBERTY System is remotely operated, enabling physicians and staff to perform procedures away from the radiation source. In the ACCESS-PVI Study, using LIBERTY demonstrated a 92% relative reduction in radiation exposure.

 

Prolonged exposure to radiation often has long-term effects that can lead to a host of health issues, including cancer, cardiovascular disease, reproductive health effects, and cataracts. This risk has also been cited as contributing to the staffing shortage in the endovascular space, and especially in interventional radiology, which currently ranks number two among specialties with highest physician shortages. It disproportionately affects women, who often cite radiation exposure and the physical demands of wearing lead aprons as barriers to entering or advancing in the field. The LIBERTY System’s wireless operated capabilities allow healthcare providers to position themselves away from the radiation source and operate in a seated position, reducing reliance on heavy PPE, thereby lessening musculoskeletal strain.

 

“Prolonged exposure to radiation and staffing shortages are rising concerns among healthcare professionals in the endovascular space,” commented Harel Gadot, CEO, President and Chairman. “We believe that these challenges strain an already overburdened health care system, impacting patient care, and widening the skills gap required to address the medical concerns. We also believe that LIBERTY can play a major role in addressing these challenges and supporting better care for both providers and their patients.”

 

LIBERTY is the only FDA cleared, single-use, remotely operated robotic system for peripheral endovascular procedures, and it is designed for precise vascular navigation while aiming to reduce radiation exposure and physical strain. The Company commenced the Limited Market Release (LMR) of the LIBERTY system in late 2025 and plans for a Full Market Release (FMR) at the Society of Interventional Radiology (SIR) conference in April 2026, allowing the Company to showcase LIBERTY with the goal to deepen market adoption.

 

 

 

 

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 world’s first FDA cleared 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 a press release highlighting its LIBERTY robotic system in the context of new American Medical Association policy on radiation safety. The company described LIBERTY’s potential to reduce occupational radiation exposure and detailed its market rollout timeline from Limited to Full Market Release.

How does Microbot Medical’s LIBERTY system address radiation exposure risks?

LIBERTY is a remotely operated endovascular robotic system designed to let physicians work away from the radiation source. In the ACCESS-PVI Study, using LIBERTY showed a 92% relative reduction in radiation exposure, supporting its role in improving safety for healthcare professionals during procedures.

What AMA policy change is relevant to Microbot Medical’s LIBERTY system?

In late 2025, the American Medical Association adopted a policy to strengthen protections for healthcare professionals and trainees facing occupational radiation exposure. Microbot states this guidance highlights the need for safer interventional solutions, aligning with the safety-focused design and capabilities of its LIBERTY robotic system.

What is Microbot Medical’s market rollout plan for the LIBERTY system?

Microbot Medical began a Limited Market Release of its LIBERTY Endovascular Robotic System in late 2025. The company plans a Full Market Release at the Society of Interventional Radiology conference in April 2026, aiming to demonstrate the system and deepen adoption among hospitals and providers.

What health issues from radiation exposure does Microbot Medical highlight?

Microbot notes that prolonged radiation exposure can contribute to cancer, cardiovascular disease, reproductive health effects, and cataracts. The company also links radiation risk and heavy protective equipment to staffing challenges, particularly in interventional radiology, and positions LIBERTY as a tool to help mitigate these concerns.

How does LIBERTY support healthcare workforce and gender-related concerns?

The filing explains that radiation exposure and the burden of lead aprons contribute to staffing shortages, disproportionately affecting women in endovascular specialties. LIBERTY’s wireless, remotely operated design allows seated operation away from the radiation source, reducing reliance on heavy protective gear and associated musculoskeletal strain.

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