Medical Device Manufacturer · IT , Assago

Trident S.R.L - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2016

Total

Cleared

Denied

Trident S.R.L has 5 FDA 510(k) cleared medical devices. Based in Assago, IT.

Last cleared in 2023. Active since 2016. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Trident S.R.L Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by The 510k Consulting, LLC as regulatory consultant.

Trident S.R.L is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Trident S.R.L

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 15, 2026