Mim Software, Inc. - FDA 510(k) Cleared Devices

Mim Software, Inc. has 22 FDA 510(k) cleared radiology devices. Based in Cleveland, US.

Latest FDA clearance: Mar 2026. Active since 2011.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.