Medica USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medica USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Purema H Hemoconcentrator - Pediatric
1
Total
1
Cleared
0
Denied
Medica USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Minnetonka, US.
Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medica USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Amarex Clinical Research, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medica USA, Inc.
1 devices