Ossacur AG
Country not established
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Colloss E Bone Void Filler Ref K051047
Regimes: 510(k) Registry: 510(k)Ossaplast Ortho Ref K050416
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ossacur AG have in the registry?
The registry currently lists 4 devices for Ossacur AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ossacur AG's devices?
Among its 4 most recently registered devices, Ossacur AG has devices listed in FDA 510(k) (4 devices).
What risk classes do Ossacur AG's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Ossacur AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ossacur AG in the registry?
The most recently registered devices listed for Ossacur AG include OSSAPLAST DENTAL (PARTICLE SIZE OF 500 TO 1000 UM TO 2000 UM), COLLOSS E BONE VOID FILLER, OSSAPLAST ORTHO and OSSAPLAST ORTHO, O.5ML, MODEL# 221 900, OSSAPLAST ORTHO, 1.0ML, MODEL# 221 901, OSSAPLAST ORTHO, 3.0ML, MODEL# 221 903.