Trident Orthopedics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trident Orthopedics - FDA 510(k) Cleared Devices
Recent clearances: Trident Extremity Fixation System
1
Total
1
Cleared
0
Denied
Trident Orthopedics has 1 FDA 510(k) cleared medical devices. Based in Millersville, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Trident Orthopedics Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wagoner Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Trident Orthopedics
1 devices