Moria, Inc. is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Moria, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Moria, Inc. has 4 FDA 510(k) cleared medical devices. Based in Antony, FR.
Historical record: 4 cleared submissions from 1998 to 2001. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Moria, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Moria, Inc.
4 devices