Seare Biomedical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seare Biomedical Corp. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Seare Biomedical Corp. has 8 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 8 cleared submissions from 1998 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Seare Biomedical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seare Biomedical Corp.
8 devices
Cleared
Dec 11, 1998
SEARE BIOMEDICAL SILICONE RODS
General & Plastic Surgery
57d
Cleared
Dec 11, 1998
SEARE BIOMEDICAL SILICONE TISSUE EXPANDER
General & Plastic Surgery
45d
Cleared
Sep 30, 1998
SEARE BIOMEDICAL CHIN IMPLANTS
General & Plastic Surgery
55d
Cleared
Sep 30, 1998
SEARE BIOMEDICAL NASAL IMPLANTS
General & Plastic Surgery
55d
Cleared
Sep 30, 1998
SEARE BIOMEDICAL PECTORALIS IMPLANT
General & Plastic Surgery
55d
Cleared
Sep 30, 1998
SEARE BIOMEDICAL MALAR IMPLANTS
General & Plastic Surgery
55d
Cleared
Sep 30, 1998
SEARE BIOMEDICAL SILICONE SHEETING
General & Plastic Surgery
30d
Cleared
Sep 30, 1998
SEARE BIOMEDICAL SILICONE BLOCK
General & Plastic Surgery
30d