Widex Hearing Aid Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Widex Hearing Aid Co., Inc. - FDA 510(k) Cleared Devices
52
Total
52
Cleared
0
Denied
Widex Hearing Aid Co., Inc. has 52 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.
Historical record: 52 cleared submissions from 1976 to 2008.
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 - Widex Hearing Aid Co., Inc.
52 devices
Cleared
Jun 27, 2008
ZEN PROGRAM (MIND 440 HEARING AID)
Ear, Nose, Throat
85d
Cleared
Jun 06, 1997
WIDEX SENSO DIGITAL (MINI CANAL)
Ear, Nose, Throat
39d
Cleared
Mar 26, 1997
WIDEX SENSO DIGITAL (CIC)
Ear, Nose, Throat
14d
Cleared
Mar 12, 1997
WIDEX MODEL SENSO DIGITAL (C9)
Ear, Nose, Throat
72d
Cleared
Jan 24, 1997
SENSO DIGITAL (C18)
Ear, Nose, Throat
25d
Cleared
Feb 27, 1996
WIDEX MODEL SENSO DIGITAL (C16)
Ear, Nose, Throat
61d
Cleared
Feb 12, 1996
WIDEX MODEL SENSO DIGITAL (C8)
Ear, Nose, Throat
46d
Cleared
Oct 18, 1995
WIDEX SENSO DIGITAL (PX)
Ear, Nose, Throat
19d
Cleared
Jun 19, 1995
WIDEX MODEL LOGO 32 (L32)
Ear, Nose, Throat
38d
Cleared
Jan 30, 1995
LX-ITC
Ear, Nose, Throat
119d
Cleared
Dec 27, 1994
WIDEX MODEL LOGO 8S
Ear, Nose, Throat
102d
Cleared
Dec 23, 1994
WIDEX MODEL LOGO - L9
Ear, Nose, Throat
51d
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