Tedan Surgical Innovations, LLC is one of 4729 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tedan Surgical Innovations, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Tedan Surgical Innovations, LLC has 2 FDA 510(k) cleared medical devices. Based in Sugar Land, US.
Historical record: 2 cleared submissions from 2014 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Tedan Surgical Innovations, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tedan Surgical Innovations, LLC
2 devices