Data / Medical devices / Israel / Microbot Medical Ltd.
Microbot Medical Ltd.: FDA-registered device maker in Yokneam Haifa, Israel, 1 510(k) clearance
Microbot Medical Ltd. is registered with the FDA (registration 3017403339) in Yokneam Haifa, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 4, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017403339
- Address
- 6 Hayozma st., Yokneam Haifa, Israel, 2069815
- Owner or operator
- Microbot Medical Ltd. (10094109)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- November 15, 2025
- Registered through
- 2026
- Brand names listed
- LIBERTY Endovascular Robotic System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Catheter Control, Steerable | DXX | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 4, 2025 | K243789 | LIBERTY Endovascular Robotic System (LIBERTYOS) | DXX | Substantially Equivalent | Microbot Medical , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 4, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.