Medical Device Manufacturer · DE , Loerrach, Baden-Wurttemberg

Medfact Engineering GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Medfact Engineering GmbH has 1 FDA 510(k) cleared medical devices. Based in Loerrach, Baden-Wurttemberg, DE.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Medfact Engineering GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Graematter, Inc. as regulatory consultant.

Medfact Engineering GmbH is one of 487 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medfact Engineering GmbH

1 devices

1-1 of 1

Data Source

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

Last updated: Sep 22, 2026