Sentec AG - FDA 510(k) Cleared Devices

Sentec AG has 5 FDA 510(k) cleared medical devices. Based in Egale, US.

Latest FDA clearance: Aug 2025. Active since 2007. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Sentec AG Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant.