Orthos Limited
United KingdomFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Osteoboost-Bma Ref K062260
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthos Limited have in the registry?
The registry currently lists 1 device for Orthos Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthos Limited's devices?
Among its 1 most recently registered device, Orthos Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Orthos Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthos Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthos Limited in the registry?
The most recently registered devices listed for Orthos Limited include OSTEOBOOST-BMA.