Medical Device Manufacturer · US , Placentia , CA

Surgical Instrument, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1988

Total

Cleared

Denied

Surgical Instrument, Inc. has 3 FDA 510(k) cleared medical devices. Based in Placentia, US.

Historical record: 3 cleared submissions from 1988 to 1994. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Surgical Instrument, Inc. Filter by specialty or product code using the sidebar.

Surgical Instrument, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Surgical Instrument, Inc.

3 devices

1-3 of 3