Zfx GmbH
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000018101 FEI 3008932779
- Devices
- 163
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 163 devicesShowing 1-50 of 163
Company details
- EUDAMED SRN
- DE-MF-000018101
- FDA FEI number
- 3008932779
- DUNS number
- 340880052
- EU VAT number
- DE260317478
- EUDAMED status
- Active
- EUDAMED registered name
- Zfx GmbH
- EUDAMED abbreviated name
- Zfx GmbH
- Registered address
- 15, Kopernikusstr., 85221, Dachau, Germany
- Website
- www.zfx-dental.com
- [email protected]
- Phone
- +49 81313324420
- PRRC contact
- Ana Leitao
Frequently asked questions
How many devices does Zfx GmbH have in the registry?
The registry currently lists 163 devices for Zfx GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zfx GmbH's devices?
Among its 50 most recently registered devices, Zfx GmbH has devices listed in EUDAMED (50 devices) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Zfx GmbH's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Zfx GmbH's devices are Class I, Class IIb and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zfx GmbH in the registry?
The most recently registered devices listed for Zfx GmbH include Zfx Titanium Screws, Zfx® Intraoral Scanbody, GenTek® and Zfx TiBases.