Robodent GmbH
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Lapdoc I Ref K061224
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Robodent GmbH have in the registry?
The registry currently lists 1 device for Robodent GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Robodent GmbH's devices?
Among its 1 most recently registered device, Robodent GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Robodent GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Robodent GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Robodent GmbH in the registry?
The most recently registered devices listed for Robodent GmbH include LAPDOC I.