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.

510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Meridian AG

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 10, 2026