Retinai Medical AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Retinai Medical AG makes
Retinai Medical AG makes RetinAI Discovery, a software device used for ophthalmic imaging analysis.
RetinAI Discovery is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
RetinAI Discovery Ref K211715
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Retinai Medical AG have in the registry?
The registry currently lists 1 device for Retinai Medical AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Retinai Medical AG's devices?
Among its 1 most recently registered device, Retinai Medical AG has devices listed in FDA 510(k) (1 device).
What risk classes do Retinai Medical AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Retinai Medical AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Retinai Medical AG in the registry?
The most recently registered devices listed for Retinai Medical AG include RetinAI Discovery.