Friandent GmbH
Country not established
- Devices
- 2
What Friandent GmbH makes
Friandent GmbH manufactures modifications and components for the XIVE 3.0 Dental Implant System, including implant fixtures designed for dental restoration procedures.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II medical devices and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Xive 3.0 Dental Implant System Ref K030639
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Friandent GmbH have in the registry?
The registry currently lists 2 devices for Friandent GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Friandent GmbH's devices?
Among its 2 most recently registered devices, Friandent GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Friandent GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Friandent GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Friandent GmbH in the registry?
The most recently registered devices listed for Friandent GmbH include MODIFICATION TO: XIVE 3.0 DENTAL IMPLANT SYSTEM, MULTIPLE and XIVE 3.0 DENTAL IMPLANT SYSTEM.