Medical Device Manufacturer · US , Lafayette , CA

Transamerican Technologies Intl. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1987

Total

Cleared

Denied

Transamerican Technologies Intl. has 4 FDA 510(k) cleared medical devices. Based in Lafayette, US.

Historical record: 4 cleared submissions from 1987 to 1997. Primary specialty: General & Plastic Surgery.

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

Transamerican Technologies Intl. 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 - Transamerican Technologies Intl.

4 devices

1-4 of 4