Oniris is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Oniris - FDA 510(k) Cleared Devices
Recent clearances: Oniris
1
Total
1
Cleared
0
Denied
Oniris has 1 FDA 510(k) cleared medical devices. Based in Rueil Malmaison, FR.
Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Oniris Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Alizée Mareczko as regulatory consultant.
FDA 510(k) Regulatory Record - Oniris
1 devices