Raed M. Ali, M.D., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Raed M. Ali, M.D., Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ali Interbody Fusion System, Ali Interbody Fusion System
2
Total
2
Cleared
0
Denied
Raed M. Ali, M.D., Inc. has 2 FDA 510(k) cleared medical devices. Based in Newport Coast, US.
Last cleared in 2021. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Raed M. Ali, M.D., Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Allenbridge Consulting and Trans1.
FDA 510(k) Regulatory Record - Raed M. Ali, M.D., Inc.
2 devices