Adeor Medical Technologies GmbH
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Meridian Cranial Perforator Ref K121253
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adeor Medical Technologies GmbH have in the registry?
The registry currently lists 1 device for Adeor Medical Technologies GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adeor Medical Technologies GmbH's devices?
Among its 1 most recently registered device, Adeor Medical Technologies GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Adeor Medical Technologies GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Adeor Medical Technologies GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adeor Medical Technologies GmbH in the registry?
The most recently registered devices listed for Adeor Medical Technologies GmbH include MERIDIAN CRANIAL PERFORATOR.