Medical Device Manufacturer · IT , Medolla, Modena

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

7 submissions · 7 cleared · Since 2011

Total

Cleared

Denied

Eurosets S.R.L has 7 FDA 510(k) cleared medical devices. Based in Medolla, Modena, IT.

Latest FDA clearance: Sep 2026. Active since 2011. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Accurate Consultants, Inc. as regulatory consultant.

Eurosets S.R.L is one of 205 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

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

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Oct 05, 2026