Medical Device Manufacturer · US , Austin , TX

Jostra Bentley - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1995

Total

Cleared

Denied

Jostra Bentley has 3 FDA 510(k) cleared medical devices. Based in Austin, US.

Historical record: 3 cleared submissions from 1995 to 1999. Primary specialty: Cardiovascular.

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

Jostra Bentley 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 - Jostra Bentley

3 devices

1-3 of 3