Aap Biomaterials GmbH
GermanyFDA applicant, unverified
- Devices
- 4
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Bonos Inject Ref K090460
Regimes: 510(k) Registry: 510(k)Vertecem Ii Cement Kit Ref K121876
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aap Biomaterials GmbH have in the registry?
The registry currently lists 4 devices for Aap Biomaterials GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aap Biomaterials GmbH's devices?
Among its 4 most recently registered devices, Aap Biomaterials GmbH has devices listed in FDA 510(k) (4 devices).
What risk classes do Aap Biomaterials GmbH's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Aap Biomaterials GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aap Biomaterials GmbH in the registry?
The most recently registered devices listed for Aap Biomaterials GmbH include BONOS R GENTA 1X20 MODEL 01-0228; BONOS R GENTA 2X20 MODEL 01-0229; BONOS R GENTA 1X40 MODEL 01-0217; BONOS R GENTA 2X40, BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60, BONOS INJECT and VERTECEM II CEMENT KIT.