Microbot Medical® Announces FDA Submission for the Commercialization of the LIBERTY® Endovascular Robotic System
MBOT 12.10.2024

About Gravity Analytica
Recent News
- 01.21.2025 - Microbot Medical® Strengthens Its Management Team in Support of the Anticipated Commercial Launch of LIBERTY®
- 01.13.2025 - Microbot Medical® Strengthens Its Commercial Capabilities with the Addition of David J. Wilson to the Board of Directors
- 01.10.2025 - Microbot Medical Closes $8.6 Million Registered Direct Offering
Recent Filings
FDA 510(k) Submission Follows the Successful Completion of the Pivotal Human Clinical Trial
FDA 510(k) Clearance Anticipated During the Second Quarter of 2025
Company Preparing to Commence Commercialization Following FDA 510(k) Clearance
The Company anticipates FDA marketing clearance during the second quarter of 2025, with
“This is a pivotal milestone for our Company, as the 510(k) submission reflects the commencement of our transition to a commercially focused company,” commented
As the world’s first single-use, fully disposable endovascular robotic system, LIBERTY®eliminates the need for large and expensive capital equipment and streamlines customers’ access to robotics. With its remote control, LIBERTY®is designed to significantly reduce radiation exposure to physicians and staff, and improve ergonomics, which has the potential to reduce the physical strain on healthcare providers. The Company also believes that LIBERTY®has the potential to lower procedure costs, increase procedure efficiency and improve the overall quality of care.
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Investor Contact:IR@microbotmedical.com

Source: Microbot Medical Inc.