Cannon U.S.A., Inc.
Country not established
- Devices
- 2
What Cannon U.S.A., Inc. makes
Cannon U.S.A., Inc. manufactures the RK-3 Auto Ref-Keratometer, a device used to measure corneal curvature and refractive error for eye examinations, and the Film Scanner 300, a diagnostic tool for digitizing and analyzing radiographic films in medical imaging.
The company’s products are regulated under FDA Class I and Class II categories, with relevant devices listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Auto Ref-Keratometer, Rk-3 Ref K942242
Regimes: 510(k) Registry: 510(k)Film Scanner 300 Ref K960839
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cannon U.S.A., Inc. have in the registry?
The registry currently lists 2 devices for Cannon U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cannon U.S.A., Inc.'s devices?
Among its 2 most recently registered devices, Cannon U.S.A., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cannon U.S.A., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cannon U.S.A., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cannon U.S.A., Inc. in the registry?
The most recently registered devices listed for Cannon U.S.A., Inc. include AUTO REF-KERATOMETER, RK-3 and FILM SCANNER 300.