Data / Medical devices / France / Axilum Robotics
Axilum Robotics: FDA-registered device maker in Schiltigheim Grand Est, France, 1 510(k) clearance
Axilum Robotics is registered with the FDA (registration 3014805507) in Schiltigheim Grand Est, France. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 17, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014805507
- Address
- 21 avenue de l'Europe, Schiltigheim Grand Est, France, 67300
- Owner or operator
- Axilum Robotics (10060211)
- Roles
- Specification developer
- First device listed
- April 11, 2019
- Registered through
- 2026
- Brand names listed
- TMS-Cobot TS MV
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electromechanical Arm For A Transcranial Magnetic Stimulation System | QFF | 2 | 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 |
|---|---|---|---|---|---|---|
| February 17, 2019 | K182768 | TMS-Cobot TS MV | QFF | Substantially Equivalent | Axilum Robotics | accessdata.fda.gov |
Compare with other makers
Updated February 17, 2019. 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.