Medical Device Manufacturer · US , New York , NY

Merete Medical GmbH - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 2005

Recent clearances: MC-Subtalar(TM) II, MetaFix LS Locking Screws, Merete Cannulated PCS, Merete CS Cortical Screws, Merete Cannulated HCS, DuoThread Scarf Screws and TwistCut Snap-Off Screws, PediatrOS RigidTack/FlexTack

24
Total
24
Cleared
0
Denied

Merete Medical GmbH has 24 FDA 510(k) cleared orthopedic devices. Based in New York, US.

Historical record: 24 cleared submissions from 2005 to 2016.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Merete Medical, Inc. and Merete Technologies, Inc..

FDA 510(k) Regulatory Record - Merete Medical GmbH

24 devices
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