Sentec AG - FDA 510(k) Cleared Devices
Recent clearances: LuMon(TM) System, Sentec Digital Monitoring System (SDMS) tCOM+, SenTec Digital Monitor, OxiVenT Sensor, V-Sign Sensor, Staysite Adhesive Pad, V-STATS PC Software including V-CareNet
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sentec AG Anesthesiology ✕
5 devices
Cleared
Aug 07, 2025
LuMon(TM) System
Anesthesiology
244d
Cleared
May 17, 2024
Sentec Digital Monitoring System (SDMS) tCOM+
Anesthesiology
273d
Cleared
Dec 17, 2015
SenTec Digital Monitor, OxiVenT Sensor, V-Sign Sensor, Staysite Adhesive Pad,...
Anesthesiology
213d
Cleared
Dec 03, 2010
SENTEC DIGITAL MONITOR, V-SIGN SENSOR AND V-SIGN SENSOR 2 WITH DIGITAL SENSOR...
Anesthesiology
170d
Cleared
Sep 12, 2007
SENTEC DIGITAL MONITORING SYSTEM
Anesthesiology
85d