Depuy France S.A.S.
Country not established
- Devices
- 7
What Depuy France S.A.S. makes
The company manufactures the DePuy Corail AMT Hip Prosthesis, a modular hip replacement system designed for total hip arthroplasty. This device features an acetabular component with a metal backing and a polyethylene liner, paired with a modular femoral stem and modular head options.
The DePuy Corail AMT Hip Prosthesis is classified as a Class II medical device under FDA regulations and is supported by a 510(k) clearance in the United States. The manufacturer is based in the US.
Catalogue
Deput Delta Xtend Reverse Shoulder Ref K120174
Regimes: 510(k) Registry: 510(k)- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Depuy Cta Reverse Shoulder System Ref K122442
Regimes: 510(k) Registry: 510(k)DePuy Corail AMT Hip Prosthesis Ref K173960
Regimes: 510(k) Registry: 510(k)Depuy Corail Amt Hip Prosthesis Ref K123991
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Depuy France S.A.S. have in the registry?
The registry currently lists 7 devices for Depuy France S.A.S.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Depuy France S.A.S.'s devices?
Among its 7 most recently registered devices, Depuy France S.A.S. has devices listed in FDA 510(k) (4 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Depuy France S.A.S.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Depuy France S.A.S.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Depuy France S.A.S. in the registry?
The most recently registered devices listed for Depuy France S.A.S. include DEPUT DELTA XTEND REVERSE SHOULDER, KAR L92530, KAR L92526 and KAR L92528.