Opto Global, Inc.
Country not established
- Devices
- 1
What Opto Global, Inc. makes
Opto Global, Inc. manufactures the Opto Global Digital Fundus Camera System Model ADS 1.5, which is a diagnostic imaging device used for capturing images of the retina.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Opto Global, Inc. have in the registry?
The registry currently lists 1 device for Opto Global, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Opto Global, Inc.'s devices?
Among its 1 most recently registered device, Opto Global, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Opto Global, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Opto Global, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Opto Global, Inc. in the registry?
The most recently registered devices listed for Opto Global, Inc. include OPTO GLOBAL DIGITAL FUNDUS CAMERA SYSTEM MODEL ADS 1.5.