Medical Device Manufacturer · CH , Thun, Bern

Meridian AG - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2002

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Meridian AG Ophthalmic ✕

4 devices

1-4 of 4

Cleared Jan 25, 2024

Ophthalmic · 167d

Cleared Sep 12, 2023

Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse

Ophthalmic · 155d

Cleared Dec 14, 2007

Ophthalmic · 73d

Cleared Sep 26, 2002

Ophthalmic · 14d

Data Source

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

Last updated: May 10, 2026