Medical Device Manufacturer · US , San Diego , CA

Triton Technology, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1988

Total

Cleared

Denied

Triton Technology, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 4 cleared submissions from 1988 to 1993. Primary specialty: Gastroenterology & Urology.

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

Triton Technology, 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 - Triton Technology, Inc.

4 devices

1-4 of 4