Osteon, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Osteon Bone Mineral Analyzer Ref K843922
Regimes: 510(k) Registry: 510(k)Modified Osteoanalyzer (# SPSHA110/220) Ref K891582
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteon, Inc. have in the registry?
The registry currently lists 2 devices for Osteon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteon, Inc.'s devices?
Among its 2 most recently registered devices, Osteon, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Osteon, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Osteon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteon, Inc. in the registry?
The most recently registered devices listed for Osteon, Inc. include OSTEON BONE MINERAL ANALYZER and MODIFIED OSTEOANALYZER (# SPSHA110/220).