Microbot Medical announces the Limited Market Release of its LIBERTY® robotic system in the U.S. after receiving FDA clearance.
Quiver AI Summary
Microbot Medical Inc. has announced the commercial availability of its LIBERTY® Endovascular Robotic System in the U.S., following its FDA clearance. The company is launching a Limited Market Release (LMR) targeting high procedure volume areas to gather real-world insights from early adopters before a Full Market Release (FMR) is expected at the Society of Interventional Radiology conference in April 2026. The introduction of LIBERTY®, the first single-use, remotely operated robotic system for endovascular procedures, has already generated strong interest and positive feedback from healthcare professionals. To support this launch, Microbot has established a logistics partnership and expanded its commercial team. CEO Harel Gadot emphasized the innovative nature of LIBERTY® and the company's commitment to quality and performance as it moves forward in the commercialization phase.
Potential Positives
- Microbot Medical Inc. has commercially launched the LIBERTY® Endovascular Robotic System in the U.S. after receiving FDA clearance, positioning itself in a new segment of the medical device market.
- The company has secured a third-party logistics partner and expanded its commercial leadership team, enhancing its infrastructure to support the successful rollout of the LIBERTY® System.
- Initial interest and positive feedback from physicians and hospital administrators indicate strong preliminary demand for LIBERTY®, supporting the decision for a Limited Market Release.
- The Full Market Release planned for April 2026 aligns with a major medical conference, providing a strategic opportunity to maximize visibility and engagement with potential users and stakeholders.
Potential Negatives
- The press release indicates that the company is only initiating a Limited Market Release (LMR) of the LIBERTY® system, suggesting a cautious and restricted approach rather than a full-scale launch.
- The future growth and commercialization of the LIBERTY® system are stated to involve significant uncertainties and risks, including market conditions and regulatory pathways, which may impact investor confidence.
- The communication of potential geopolitical disruptions and their impact on the company’s operations may raise concerns about the stability and predictability of its business environment.
FAQ
What is the LIBERTY® Endovascular Robotic System?
The LIBERTY® is the first FDA cleared single-use, remotely operated robotic system for peripheral endovascular procedures.
When will LIBERTY® be available in the U.S. market?
The LIBERTY® System is now commercially available in the U.S. following its Limited Market Release.
What regions will the LIBERTY® Limited Market Release target?
The Limited Market Release will focus on selected high procedure volume regions with preliminary demand for LIBERTY®.
What feedback has LIBERTY® received from healthcare professionals?
Physicians and hospital administrators have expressed overwhelmingly positive feedback regarding the LIBERTY® System.
When is the expected Full Market Release of LIBERTY®?
The Full Market Release is expected during the Society of Interventional Radiology meeting in April 2026.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$MBOT Hedge Fund Activity
We have seen 32 institutional investors add shares of $MBOT stock to their portfolio, and 17 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- VANGUARD GROUP INC added 1,309,473 shares (+176.7%) to their portfolio in Q2 2025, for an estimated $3,299,871
- CIBC PRIVATE WEALTH GROUP LLC added 612,000 shares (+inf%) to their portfolio in Q2 2025, for an estimated $1,542,240
- MORGAN STANLEY added 136,757 shares (+650.8%) to their portfolio in Q2 2025, for an estimated $344,627
- BLACKROCK, INC. added 85,077 shares (+36.0%) to their portfolio in Q2 2025, for an estimated $214,394
- GEODE CAPITAL MANAGEMENT, LLC added 78,121 shares (+24.7%) to their portfolio in Q2 2025, for an estimated $196,864
- DNB ASSET MANAGEMENT AS added 77,965 shares (+67.9%) to their portfolio in Q2 2025, for an estimated $196,471
- SUSQUEHANNA INTERNATIONAL GROUP, LLP removed 72,341 shares (-69.4%) from their portfolio in Q2 2025, for an estimated $182,299
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
$MBOT Analyst Ratings
Wall Street analysts have issued reports on $MBOT in the last several months. We have seen 1 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
Here are some recent analyst ratings:
- HC Wainwright & Co. issued a "Buy" rating on 09/11/2025
To track analyst ratings and price targets for $MBOT, check out Quiver Quantitative's $MBOT forecast page.
Full Release
Company Completes the Required Infrastructure to Support the Introduction of LIBERTY® to the U.S. Market with the Hiring of the Core Commercial Team and Establishing Logistic Partnership
Interest and Overwhelmingly Positive Feedback from Physicians and Hospital Administrators at Recent Meetings Validates Limited Market Release of LIBERTY ®
HINGHAM, Mass., Nov. 05, 2025 (GLOBE NEWSWIRE) -- Microbot Medical Inc. (Nasdaq: MBOT), developer and distributor of the innovative LIBERTY ® Endovascular Robotic System, announced that its LIBERTY ® System, the first FDA cleared single-use, remotely operated robotic system for peripheral endovascular procedures, is now commercially available in the U.S. The Limited Market Release (LMR) will introduce LIBERTY ® to selected high procedure volume regions where the Company already experienced preliminary demand for LIBERTY ® . The LMR will focus on collecting real-world insights from potential high-volume users to guide responsible growth and ensure consistent quality and performance, leading to the expected Full Market Release (FMR) during the Society of Interventional Radiology (SIR), the largest U.S. medical conference for Interventional Radiology, in April 2026.
“We are excited to enter the commercialization phase of LIBERTY ® . We are building a new robotic category with the introduction of LIBERTY ® , the world’s first single-use robotic system. Launching just weeks after announcing FDA clearance, we believe that we have demonstrated the strength of our team and the unique innovation behind LIBERTY ® ,” commented Harel Gadot, CEO, President and Chairman. “Building on the strong interest and feedback we have received so far from physicians and hospital administrators, the limited market release is expected to enable us to responsibly support early adopters and lay the groundwork for a full market launch at the Society of Interventional Radiology meeting in April.”
Since receiving the FDA 510(k) clearance for the LIBERTY ® System in September, the Company has advanced its commercial readiness by securing a third-party logistics partner and expanding its commercial leadership team to ensure a fully supported and successful limited market release.
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.
Commercialization Robotics MedTech MBOT News Endovascular Robotics Medical Robotics Innovation
Learn more at www.microbotmedical.com and connect on LinkedIn and X .
Safe Harbor
Statements to future financial and/or operating results, 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:
[email protected]
[email protected]
A video accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/f9906051-4491-4f55-9a79-2d0e2b0d1413