Koehrer Medical Engineering GmbH is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Koehrer Medical Engineering GmbH - FDA 510(k) Cleared Devices
Recent clearances: EndoColibri
1
Total
1
Cleared
0
Denied
Koehrer Medical Engineering GmbH has 1 FDA 510(k) cleared medical devices. Based in Neuss, DE.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Koehrer Medical Engineering GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Koehrer Medical Engineering GmbH
1 devices