Osteogenics Co.
Also registered as Osteogenics, Inc.
Country not established
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Star Temporary Wound Cover Ref K983753
Regimes: 510(k) Registry: 510(k)Bonesource Hydroxyapatite Cement (Hac) Ref K964537
Regimes: 510(k) Registry: 510(k)Xtac Ref K061934
Regimes: 510(k) Registry: 510(k)Bonesource Hydroxyapatite Cement (Hac) Ref K953339
Regimes: 510(k) Registry: 510(k)Cytoplast Regentex Titanium 250 Ref K972278
Regimes: 510(k) Registry: 510(k)Cytoplast Gbr Ref K964342
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteogenics Co. have in the registry?
The registry currently lists 6 devices for Osteogenics Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteogenics Co.'s devices?
Among its 6 most recently registered devices, Osteogenics Co. has devices listed in FDA 510(k) (6 devices).
What risk classes do Osteogenics Co.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Osteogenics Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteogenics Co. in the registry?
The most recently registered devices listed for Osteogenics Co. include STAR TEMPORARY WOUND COVER, BONESOURCE HYDROXYAPATITE CEMENT (HAC), XTAC and CYTOPLAST REGENTEX TITANIUM 250.