Depuy, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 307
What Depuy, Inc. makes
The company manufactures orthopedic implants and fixation systems, including femoral prostheses (revision and primary), cobalt-chrome hip components, titanium cross-pin fixation devices, and cannulated screw systems for bone stabilization. It also produces bone cement mixing systems, intramedullary nails, hemiarthroplasty shoulder prostheses, fracture stems, and zirconia total hip ball head systems, as well as collarless lateralized femoral hip implants.
These devices are regulated under FDA classifications, including Class I, Class II, and Class III, with many cleared via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Search and filter all 307 devicesShowing 1-50 of 307
Frequently asked questions
How many devices does Depuy, Inc. have in the registry?
The registry currently lists 307 devices for Depuy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Depuy, Inc.'s devices?
Among its 50 most recently registered devices, Depuy, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Depuy, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Depuy, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Depuy, Inc. in the registry?
The most recently registered devices listed for Depuy, Inc. include DELTA SHOULDER, SYNATOMIC REVISION FEMORAL PROSTHESIS, POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS and COBALT CHROME GEMINI.