Medical Device Manufacturer · US , Mchenry , IL

Tridak Division of Indicon, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1984

Total

Cleared

Denied

Tridak Division of Indicon, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1984 to 1990. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Tridak Division of Indicon, Inc. Filter by specialty or product code using the sidebar.

Tridak Division of Indicon, 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 - Tridak Division of Indicon, Inc.

7 devices

1-7 of 7