TeDan Surgical Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
TeDan Surgical Innovations, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Phantom XL Insulated Dilators
1
Total
1
Cleared
0
Denied
TeDan Surgical Innovations, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sugar Land, US.
Last cleared in 2023. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by TeDan Surgical Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - TeDan Surgical Innovations, Inc.
1 devices