Medical Device Manufacturer · US , Mchenry , IL

Oticon Corp. - FDA 510(k) Cleared Devices

57 submissions · 57 cleared · Since 1978
57
Total
57
Cleared
0
Denied

Oticon Corp. has 57 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.

Historical record: 57 cleared submissions from 1978 to 1996.

Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Oticon Corp.

57 devices
1-12 of 57

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