Medtronic, Ireland - FDA 510(k) Cleared Devices

Medtronic, Ireland has 9 FDA 510(k) cleared medical devices. Based in Shoreview, US.

Latest FDA clearance: Aug 2026. Active since 2006. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Medtronic, Ireland Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Medtronic Ireland as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.