Schlumbohm GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Schlumbohm GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: EndoPilot2
1
Total
1
Cleared
0
Denied
Schlumbohm GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Brokstedt, DE.
Last cleared in 2021. Active since 2021. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Schlumbohm GmbH & Co. KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Schlumbohm GmbH & Co. KG
1 devices