Medical Device Manufacturer · US , San Diego , CA

Grundler GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2013

Recent clearances: HUMICARE D900

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Grundler GmbH Anesthesiology ✕

1 devices

1-1 of 1

Cleared May 21, 2013

Anesthesiology · 259d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 17, 2026