Medical Device Manufacturer · US , Monarch Beach , CA

Trylon Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1995

Total

Cleared

Denied

Trylon Corp. has 7 FDA 510(k) cleared medical devices. Based in Monarch Beach, US.

Historical record: 7 cleared submissions from 1995 to 2004. Primary specialty: Obstetrics & Gynecology.

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

Trylon Corp. is one of 25405 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Trylon Corp.

7 devices

1-7 of 7