Eberle GmbH & Co. KG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Eberle GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Wurmberg, DE.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Eberle GmbH & Co. KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Visamed GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Eberle GmbH & Co. KG
1 devices