Medical Device Manufacturer · IT , Assago

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

5 submissions · 5 cleared · Since 2016
5
Total
5
Cleared
0
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.

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