Medical Device Manufacturer · CH , Bern

Retinai Medical AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Retinai Medical AG has 1 FDA 510(k) cleared medical devices. Based in Bern, CH.

Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Retinai Medical AG Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Retinai Medical AG

1 devices

1-1 of 1