Oticon Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oticon Corp. - FDA 510(k) Cleared Devices
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
Cleared
Nov 27, 1996
PRIMOFOCUS COMPACT
Ear, Nose, Throat
68d
Cleared
Aug 05, 1993
OTICON MF
Ear, Nose, Throat
64d
Cleared
Aug 06, 1992
BTE HEARING AID OTICON MODEL: MULTIFOCUS POWER
Ear, Nose, Throat
30d
Cleared
Aug 06, 1992
BTE HEARING AID PERSONIC 410
Ear, Nose, Throat
22d
Cleared
Aug 06, 1992
BTE HEARING AID PERSONIC 425
Ear, Nose, Throat
23d
Cleared
Jul 06, 1992
A-ZILICONE
Ear, Nose, Throat
573d
Cleared
Nov 01, 1990
OTICAON BTE MODEL E34P
Ear, Nose, Throat
20d
Cleared
Jul 09, 1990
CUSTOM IN-THE-EAR HEARING AID OTICON MODEL: P
Ear, Nose, Throat
28d
Cleared
Jun 14, 1990
CUSTOM ITE HEARING AID MODELS C AND M
Ear, Nose, Throat
16d
Cleared
Jun 14, 1990
CUSTOM ITE HEARING AID MODEL: H
Ear, Nose, Throat
16d
Cleared
Jun 14, 1990
CUSTOM ITE HEARING AID MODELS F AND L
Ear, Nose, Throat
16d
Cleared
Apr 10, 1990
OTICON BTE HEARING AID (BEHIND-THE-EAR), MODEL E44
Ear, Nose, Throat
21d
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