Medical Device Manufacturer · DE , Luebeck

Dr?gerwerk AG & Co KGaA - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2022

Total

Cleared

Denied

Dr?gerwerk AG & Co KGaA has 5 FDA 510(k) cleared medical devices. Based in Luebeck, DE.

Latest FDA clearance: May 2026. Active since 2022. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Dr?gerwerk AG & Co KGaA Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Drägerwerk AG & Co. KGaA and Drägerwerk AG Co. Kgaa.

Dr?gerwerk AG & Co KGaA is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dr?gerwerk AG & Co KGaA

5 devices

1-5 of 5

Data Source

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

Last updated: Jun 05, 2026