Covidien (Part of Medtronic) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Covidien (Part of Medtronic) - FDA 510(k) Cleared Devices
Recent clearances: Tri-staple 2.0™ Reloads, Signia™ Circular Adapter (Standard Length) (SIGCIRSTND)
2
Total
2
Cleared
0
Denied
Covidien (Part of Medtronic) has 2 FDA 510(k) cleared medical devices. Based in North Haven, US.
Latest FDA clearance: Apr 2026. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Covidien (Part of Medtronic) Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Covidien (Part of Medtronic)
2 devices