Trans1 is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trans1 - FDA 510(k) Cleared Devices
Recent clearances: TranS1 AxiaLIF Plus System, TranS1 Interbody Fusion System
2
Total
2
Cleared
0
Denied
Trans1 has 2 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Trans1 Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trans1
2 devices