Medtronic Minimed, Inc. - FDA 510(k) Cleared Devices

Medtronic Minimed, Inc. has 8 FDA 510(k) cleared medical devices. Based in Northridge, US.

Latest FDA clearance: Mar 2026. Active since 2007. Primary specialty: Chemistry.

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

2 devices have linked clinical trials registered on ClinicalTrials.gov. 4 submissions have an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.