Ulrich GmbH & Co. KG - FDA 510(k) Cleared Devices

Ulrich GmbH & Co. KG has 23 FDA 510(k) cleared medical devices. Based in Ulm, DE.

Latest FDA clearance: Nov 2025. Active since 2005. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Ulrich GmbH & Co. KG Filter by specialty or product code using the sidebar.

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