Medical Device Manufacturer · US , Pittsburgh , PA

Dymax Corp - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1985

Total

Cleared

Denied

Dymax Corp has 7 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.

Historical record: 7 cleared submissions from 1985 to 2003. Primary specialty: Radiology.

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

510(k) submissions have been managed by Citech as regulatory consultant.

Dymax Corp is one of 9730 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dymax Corp

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 11, 2026