Oak Tree Engineering, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oak Tree Engineering, LLC - FDA 510(k) Cleared Devices
Recent clearances: OAKTREE Anterior Lumbar Plate and Screw System, Fixxsure Anterior Lumbar Plate and Screw System
2
Total
2
Cleared
0
Denied
Oak Tree Engineering, LLC has 2 FDA 510(k) cleared medical devices. Based in Huntington Beach, US.
Last cleared in 2022. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Oak Tree Engineering, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Consultant as regulatory consultant.
FDA 510(k) Regulatory Record - Oak Tree Engineering, LLC
2 devices