Titan Spine, LLC is one of 13766 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Titan Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion Device, Endoskeleton TO Interbody Fusion Device (IBD), Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device
Titan Spine, LLC has 14 FDA 510(k) cleared orthopedic devices. Based in Mequon, US.
Historical record: 14 cleared submissions from 2008 to 2018.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Memphis Regulatory Consulting, LLC, Mrc/X, LLC and Mrc-X, LLC.