Noviace Corporation
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Normed Compression Bone Screw System Ref K032634
Regimes: 510(k) Registry: 510(k)Osteosorb Tack Fixation System Ref K030989
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Noviace Corporation have in the registry?
The registry currently lists 2 devices for Noviace Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Noviace Corporation's devices?
Among its 2 most recently registered devices, Noviace Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Noviace Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Noviace Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Noviace Corporation in the registry?
The most recently registered devices listed for Noviace Corporation include NORMED COMPRESSION BONE SCREW SYSTEM and OSTEOSORB TACK FIXATION SYSTEM.