Telstar Electronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Telstar Electronics, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Telstar Electronics, Inc. has 11 FDA 510(k) cleared ear, nose, throat devices. Based in Longwood, US.
Historical record: 11 cleared submissions from 1987 to 1989.
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 - Telstar Electronics, Inc.
11 devices
Cleared
Jun 06, 1989
TELSTAR MODEL 1/3 ITE HEARING AID
Ear, Nose, Throat
57d
Cleared
Jun 06, 1989
TELSTAR MODEL F ITE HEARING AID
Ear, Nose, Throat
57d
Cleared
Jun 06, 1989
TELSTAR MODEL C ITE HEARING AID
Ear, Nose, Throat
57d
Cleared
Jun 06, 1989
TELSTAR MODEL PP ITE HEARING AID
Ear, Nose, Throat
57d
Cleared
Oct 27, 1987
TELSTAR PREWIRE SERIES
General & Plastic Surgery
175d
Cleared
Sep 29, 1987
TELSTAR MODEL PP
Ear, Nose, Throat
46d
Cleared
Jun 08, 1987
TELSTAR MODEL FS HEARING AID
Ear, Nose, Throat
49d
Cleared
Jun 05, 1987
TELSTAR MODEL F3TS HEARING AID
Ear, Nose, Throat
46d
Cleared
Jun 05, 1987
FULL SHELL ITE HEARING AID
Ear, Nose, Throat
46d
Cleared
Jun 05, 1987
TELSTAR MODEL C HEARING AID
Ear, Nose, Throat
46d
Cleared
May 19, 1987
TELSTAR MODEL 0/3 HEARING AID
Ear, Nose, Throat
29d