Sentinel Medical Technologies, is one of 16141 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sentinel Medical Technologies, - FDA 510(k) Cleared Devices
Recent clearances: TraumaGuard Intra-Abdominal Pressure-Sensing System (000-0221)
1
Total
1
Cleared
0
Denied
Sentinel Medical Technologies, has 1 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Sentinel Medical Technologies, Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sentinel Medical Technologies,
1 devices