Movmedix S.A.S.
Country not established FDA establishment FEI 1000422168
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Lars Acj Ref K253115
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000422168
- Address
- 5 rue de la Fontaine, ARC SUR TILLE Bourgogne-Franche-Comte
Frequently asked questions
How many devices does Movmedix S.A.S have in the registry?
The registry currently lists 1 device for Movmedix S.A.S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Movmedix S.A.S's devices?
Among its 1 most recently registered device, Movmedix S.A.S has devices listed in FDA 510(k) (1 device).
What risk classes do Movmedix S.A.S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Movmedix S.A.S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Movmedix S.A.S in the registry?
The most recently registered devices listed for Movmedix S.A.S include LARS ACJ.