Medical Device Manufacturer · CH , Thun, Bern

Meridian AG - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2002

Total

Cleared

Denied

Meridian AG has 6 FDA 510(k) cleared medical devices. Based in Thun, Bern, CH.

Latest FDA clearance: Jan 2024. Active since 2002. Primary specialty: Ophthalmic.

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

FDA 510(k) cleared devices by Meridian AG

6 devices

1-6 of 6