Retinai Medical AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Retinai Medical AG - FDA 510(k) Cleared Devices
Recent clearances: RetinAI Discovery
1
Total
1
Cleared
0
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) Regulatory Record - Retinai Medical AG
1 devices