Triopsy Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Triopsy Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Triopsy Actuator (TMSDGB)
1
Total
1
Cleared
0
Denied
Triopsy Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mankato, US.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Triopsy Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eri Group as regulatory consultant.
FDA 510(k) Regulatory Record - Triopsy Medical, Inc.
1 devices