UPlanner B.V. - Presurgeo
NetherlandsFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
SkeletonPlanner Ref K260206
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does UPlanner B.V. - Presurgeo have in the registry?
The registry currently lists 1 device for UPlanner B.V. - Presurgeo. Devices recorded under merged duplicate company entries are counted once.
Which registries list UPlanner B.V. - Presurgeo's devices?
Among its 1 most recently registered device, UPlanner B.V. - Presurgeo has devices listed in FDA 510(k) (1 device).
What risk classes do UPlanner B.V. - Presurgeo's devices fall under?
Among its 1 most recently registered device, the classes recorded for UPlanner B.V. - Presurgeo's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from UPlanner B.V. - Presurgeo in the registry?
The most recently registered devices listed for UPlanner B.V. - Presurgeo include SkeletonPlanner.