Vexim SA
FranceFDA applicant, unverified
- Devices
- 1
What Vexim SA makes
Vexim SA manufactures the SpineJack Expansion Kit, which is a medical device used for spinal procedures.
The company is based in the US, and its portfolio includes Class II devices that are listed in the FDA 510(k) regulatory registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
SpineJack Expansion Kit Ref K181262
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vexim SA have in the registry?
The registry currently lists 1 device for Vexim SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vexim SA's devices?
Among its 1 most recently registered device, Vexim SA has devices listed in FDA 510(k) (1 device).
What risk classes do Vexim SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vexim SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vexim SA in the registry?
The most recently registered devices listed for Vexim SA include SpineJack Expansion Kit.