Cogentix Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cogentix Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PrimeSight UltraView System, PrimeSight™ UNITY 9000 Video Processor, PrimeSight™ UNITY 9100 Video Processor
2
Total
2
Cleared
0
Denied
Cogentix Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Orangeburg, US.
Latest FDA clearance: Apr 2026. Active since 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cogentix Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cogentix Medical, Inc.
2 devices