Omni Hearing Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omni Hearing Systems - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Omni Hearing Systems has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1981 to 1984. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Omni Hearing Systems Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Omni Hearing Systems
7 devices
Cleared
Nov 01, 1984
IN THE CANAL HEARING AID RC, REDICANAL
Ear, Nose, Throat
27d
Cleared
Dec 08, 1983
IN THE EAR HEARING AID OMNI 100
Ear, Nose, Throat
72d
Cleared
Nov 14, 1983
BEHIND THE EAR ASP-BB
Ear, Nose, Throat
48d
Cleared
Nov 14, 1983
TEL-STAR NUWAY & GENERIC E ASP-BP
Ear, Nose, Throat
40d
Cleared
Mar 07, 1983
BEHIND THE EAR HEARING AID OMNI #OS
Ear, Nose, Throat
20d
Cleared
Jan 07, 1983
TEL-STAR NU-WAY & GENERIC E
Ear, Nose, Throat
73d
Cleared
May 27, 1981
OMNI
Ear, Nose, Throat
29d