Moria SA is one of 247 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Moria SA - FDA 510(k) Cleared Devices
Recent clearances: EPI K Console, EPI-K
5
Total
5
Cleared
0
Denied
Moria SA has 5 FDA 510(k) cleared medical devices. Based in Antony, FR.
Historical record: 5 cleared submissions from 2002 to 2017. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Moria SA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Association, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Moria SA
5 devices