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