Magne-Dent
Country not established
- Devices
- 1
What Magne-Dent makes
Magne-Dent makes the MAGNE-DENT device, which is a magnetic dental product used for securing or stabilizing dental prosthetics or components.
The MAGNE-DENT device is classified as Class I and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Magne-Dent Ref K840600
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Magne-Dent have in the registry?
The registry currently lists 1 device for Magne-Dent. Devices recorded under merged duplicate company entries are counted once.
Which registries list Magne-Dent's devices?
Among its 1 most recently registered device, Magne-Dent has devices listed in FDA 510(k) (1 device).
What risk classes do Magne-Dent's devices fall under?
Among its 1 most recently registered device, the classes recorded for Magne-Dent's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Magne-Dent in the registry?
The most recently registered devices listed for Magne-Dent include MAGNE-DENT.