Medical Device Manufacturer · US , Salt Lake City , UT

Seare Biomedical Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1998

Recent clearances: SEARE BIOMEDICAL SILICONE RODS, SEARE BIOMEDICAL SILICONE TISSUE EXPANDER, SEARE BIOMEDICAL CHIN IMPLANTS

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.

Seare Biomedical Corp. is one of 7811 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Seare Biomedical Corp.

8 devices

1-8 of 8

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