Telesonic, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Telesonic, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Telesonic, Inc. has 12 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1980 to 1987.
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 - Telesonic, Inc.
12 devices
Cleared
Dec 22, 1987
TELESONIC BODY STIMULATOR
Physical Medicine
173d
Cleared
Jan 19, 1982
POST-AURICULAR HEARING AID MODEL P-101
Ear, Nose, Throat
56d
Cleared
Jan 19, 1982
POST-AURICULAR HEARING AID MODEL S-101
Ear, Nose, Throat
56d
Cleared
Dec 31, 1981
CUSTOM-IN-THE-EAR HEARING AID
Ear, Nose, Throat
37d
Cleared
Dec 31, 1981
POST-AURICULAR HEARING AID MODEL ASP-103
Ear, Nose, Throat
36d
Cleared
Jul 01, 1981
TELESONIC & ARCON
Ear, Nose, Throat
76d
Cleared
Nov 12, 1980
TELESONIC, ARCON & SOUNDEX ASP 102
Ear, Nose, Throat
22d
Cleared
Nov 12, 1980
TELESONIC ARCON & SOUNDEX ASP 101
Ear, Nose, Throat
22d
Cleared
May 28, 1980
TELESONIC, SOUNDEX & GENERIC V-101
Ear, Nose, Throat
22d
Cleared
May 28, 1980
TELESONIC, GENERIC & SOUNDEX C-102
Ear, Nose, Throat
22d
Cleared
Feb 11, 1980
TELESONIC (HEARING AID)
Ear, Nose, Throat
26d
Cleared
Jan 23, 1980
TELESONIC V-101
Ear, Nose, Throat
28d