Omega Silicone, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omega Silicone, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Omega Silicone, Inc. has 5 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.
Historical record: 5 cleared submissions from 1987 to 1987. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Omega Silicone, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Omega Silicone, Inc.
5 devices
Cleared
Jun 08, 1987
OMEGA NASAL SEPTAL BUTTON
Ear, Nose, Throat
82d
Cleared
May 11, 1987
OMEGA SILICONE CHIN IMPLANT
General & Plastic Surgery
54d
Cleared
May 11, 1987
OMEGA BIVALVE NASAL SPLINTS
General & Plastic Surgery
54d
Cleared
Apr 13, 1987
OMEGA DORSAL COLUMELLA IMPLANTS
General & Plastic Surgery
26d
Cleared
Apr 10, 1987
OMEGA EXTENDED MALAR AND OMEGA CONTOURED MALAR
General & Plastic Surgery
23d