Medical Device Manufacturer · US , Mchenry , IL

Oticon Corp. - FDA 510(k) Cleared Devices

57 submissions · 57 cleared · Since 1978

Recent clearances: PRIMOFOCUS COMPACT, OTICON MF, BTE HEARING AID OTICON MODEL: MULTIFOCUS POWER

57

Total

57

Cleared

0

Denied

FDA 510(k) Regulatory Record - Oticon Corp. Ear, Nose, Throat ✕

56 devices

1-12 of 56

Cleared Nov 27, 1996

PRIMOFOCUS COMPACT

Ear, Nose, Throat · 68d

Cleared Aug 05, 1993

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

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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