Medical Device Manufacturer · US , Mansfield , MA

Covidien LP - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2009

Total

Cleared

Denied

Covidien LP has 4 FDA 510(k) cleared medical devices. Based in Mansfield, US.

Latest FDA clearance: Aug 2026. Active since 2009. Primary specialty: Anesthesiology.

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

Covidien LP is one of 18365 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Covidien LP

4 devices

1-4 of 4