Depuy Ace
Country not established
- Devices
- 2
What Depuy Ace makes
Depuy Ace manufactures orthopedic intramedullary nails for humeral fractures, including proximal and antegrade/retrograde configurations designed for internal fixation of the humerus.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Ace Proximal Humeral Nail System Ref K033806
Regimes: 510(k) Registry: 510(k)Ace Antegrade Retrograde Humeral Nail System Ref K033878
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Depuy Ace have in the registry?
The registry currently lists 2 devices for Depuy Ace. Devices recorded under merged duplicate company entries are counted once.
Which registries list Depuy Ace's devices?
Among its 2 most recently registered devices, Depuy Ace has devices listed in FDA 510(k) (2 devices).
What risk classes do Depuy Ace's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Depuy Ace's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Depuy Ace in the registry?
The most recently registered devices listed for Depuy Ace include ACE PROXIMAL HUMERAL NAIL SYSTEM and ACE ANTEGRADE RETROGRADE HUMERAL NAIL SYSTEM.