Minnesota Medical Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Minnesota Medical Technologies - FDA 510(k) Cleared Devices
Recent clearances: Minnesota Medical Technologies Fecal Incontinence Insert (My Miracle)
1
Total
1
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Minnesota Medical Technologies
1 devices