Medical Device Manufacturer · US , Egale , WI

Sentec AG - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007

Total

Cleared

Denied

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.

Sentec AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sentec AG

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 27, 2026