Metamorphosis GmbH
GermanyFDA applicant, unverified FDA FEI 3042243683
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
AIAS Cephalon Ref K252214
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3042243683
- DUNS number
- 315129327
- Address
- Technologiepark 9, Paderborn North Rhine-Westphalia
Frequently asked questions
How many devices does Metamorphosis GmbH have in the registry?
The registry currently lists 2 devices for Metamorphosis GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Metamorphosis GmbH's devices?
Among its 2 most recently registered devices, Metamorphosis GmbH has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Metamorphosis GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Metamorphosis GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Metamorphosis GmbH in the registry?
The most recently registered devices listed for Metamorphosis GmbH include VELYS Trauma 10.037.001 and AIAS Cephalon.