Oticon A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Oticon A/S - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Oticon A/S has 2 FDA 510(k) cleared medical devices. Based in Thisted, DK.
Historical record: 2 cleared submissions from 1995 to 2014. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Oticon A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oticon A/S
2 devices