Medical Device Manufacturer · US , East Providence , RI

Instantron - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1993

Total

Cleared

Denied

Instantron has 7 FDA 510(k) cleared medical devices. Based in East Providence, US.

Historical record: 7 cleared submissions from 1993 to 1994. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Instantron Filter by specialty or product code using the sidebar.

Instantron 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 - Instantron

7 devices

1-7 of 7