Bego U.S.A.
Country not established
- Devices
- 7
What Bego U.S.A. makes
Bego U.S.A. manufactures dental casting alloys, including WIROBOND C, AUROLLOYD KF, BEGOPAL, BIO PONTOSTAR, PLATINLLOYD 100, BEGOCER G, and GOLD DENTAL CASTING ALLOYS.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Wirobond C Ref K032136
Regimes: 510(k) Registry: 510(k)Aurolloyd Kf Ref K983080
Regimes: 510(k) Registry: 510(k)Begopal Ref K983078
Regimes: 510(k) Registry: 510(k)Bio Pontostar Ref K983077
Regimes: 510(k) Registry: 510(k)Platinlloyd 100 Ref K983079
Regimes: 510(k) Registry: 510(k)Begocer G Ref K983082
Regimes: 510(k) Registry: 510(k)Gold Dental Casting Alloys Ref K033279
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bego U.S.A. have in the registry?
The registry currently lists 7 devices for Bego U.S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bego U.S.A.'s devices?
Among its 7 most recently registered devices, Bego U.S.A. has devices listed in FDA 510(k) (7 devices).
What risk classes do Bego U.S.A.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Bego U.S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bego U.S.A. in the registry?
The most recently registered devices listed for Bego U.S.A. include WIROBOND C, AUROLLOYD KF, BEGOPAL and BIO PONTOSTAR.