Oniris - FDA 510(k) Cleared Devices
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.
1 devices