Implant Solutions Pty Ltd (Aka Osteon Medical)
AustraliaFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Osteon Precision Milled Suprastructure Ref K221019
Regimes: 510(k) Registry: 510(k)Osteon Precision Milled Suprastructure Ref K233083
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Implant Solutions Pty Ltd (Aka Osteon Medical) have in the registry?
The registry currently lists 2 devices for Implant Solutions Pty Ltd (Aka Osteon Medical). Devices recorded under merged duplicate company entries are counted once.
Which registries list Implant Solutions Pty Ltd (Aka Osteon Medical)'s devices?
Among its 2 most recently registered devices, Implant Solutions Pty Ltd (Aka Osteon Medical) has devices listed in FDA 510(k) (2 devices).
What risk classes do Implant Solutions Pty Ltd (Aka Osteon Medical)'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Implant Solutions Pty Ltd (Aka Osteon Medical)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Implant Solutions Pty Ltd (Aka Osteon Medical) in the registry?
The most recently registered devices listed for Implant Solutions Pty Ltd (Aka Osteon Medical) include Osteon Precision Milled Suprastructure.