Eurodent S.P.A.
Country not established
- Devices
- 1
What Eurodent S.P.A. makes
Eurodent S.P.A. manufactures the ABSOLUTE AMERICA, which is a dental device.
This product is classified as a Class I medical device and is listed within the FDA 510(k) registry. The company is based in the United States.
Catalogue
Absolute America Ref K050571
510(k) 510(k)
Frequently asked questions
How many devices does Eurodent S.P.A. have in the registry?
The registry currently lists 1 device for Eurodent S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eurodent S.P.A.'s devices?
Among its 1 most recently registered device, Eurodent S.P.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Eurodent S.P.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eurodent S.P.A.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Eurodent S.P.A. in the registry?
The most recently registered devices listed for Eurodent S.P.A. include ABSOLUTE AMERICA.