Medical Device Manufacturer · FR , Antony

Moria SA - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2002

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Moria SA Ophthalmic ✕

5 devices

1-5 of 5

Cleared Oct 26, 2017

Ophthalmic · 29d

Cleared Mar 25, 2005

Ophthalmic · 128d

Cleared Jun 18, 2004

M3 MICROKERATOME

Ophthalmic · 281d

Cleared Mar 31, 2004

ONEUSE- PLUS MICROKERATOME

Ophthalmic · 51d

Cleared Sep 27, 2002

M2 SINGLE USE MICROKERTOME

Ophthalmic · 56d

Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Apr 27, 2026