Sentinel Medical Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sentinel Medical Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: TraumaGuard Intra-abdominal Pressure Sensing System, TraumaGuard Intra-abdominal Pressure Sensing System
2
Total
2
Cleared
0
Denied
Sentinel Medical Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Latest FDA clearance: Apr 2024. Active since 2021. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Sentinel Medical Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tpl Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Sentinel Medical Technologies, LLC
2 devices