Minnesota Medical Technologies - FDA 510(k) Cleared Devices

Minnesota Medical Technologies has 1 FDA 510(k) cleared medical devices. Based in Stewartville, US.

Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Minnesota Medical Technologies Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Sachs & Associates, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.