Usbiomaterials Corp.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Perioglass Ref K930115
Regimes: 510(k) Registry: 510(k)Perioglas- Bioglass Bone Graft Particulate Ref K992416
Regimes: 510(k) Registry: 510(k)Butler Gum Prophy Paste With Novamin Ref K024343
Regimes: 510(k) Registry: 510(k)Novabone-Bioglass Bone Graft Particulate Ref K000149
Regimes: 510(k) Registry: 510(k)Perioglas - Bioglass Bone Graft Particulate Ref K962494
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Usbiomaterials Corp. have in the registry?
The registry currently lists 5 devices for Usbiomaterials Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Usbiomaterials Corp.'s devices?
Among its 5 most recently registered devices, Usbiomaterials Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Usbiomaterials Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Usbiomaterials Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Usbiomaterials Corp. in the registry?
The most recently registered devices listed for Usbiomaterials Corp. include PERIOGLASS, PERIOGLAS- BIOGLASS BONE GRAFT PARTICULATE, BUTLER GUM PROPHY PASTE WITH NOVAMIN and NOVABONE-BIOGLASS BONE GRAFT PARTICULATE.