Inex
FranceFDA applicant, unverified
- Devices
- 1
What Inex makes
Inex manufactures suction lipoplasty accessories.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Suction Lipoplasty Accessories Ref K132353
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inex have in the registry?
The registry currently lists 1 device for Inex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inex's devices?
Among its 1 most recently registered device, Inex has devices listed in FDA 510(k) (1 device).
What risk classes do Inex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Inex's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inex in the registry?
The most recently registered devices listed for Inex include SUCTION LIPOPLASTY ACCESSORIES.