Regulatory Spine Top Stories SurGenTec Secures FDA 510(k) Clearance for TiLink™ SI joint fusion- Now Navigation Compatible byJosh SandbergApril 15, 2026
Regulatory Spine SurGenTec® Secures FDA Clearance for ION-C™ Facet Fixation System — Designed to Support Fusion While Preserving Alignment byTim AllenJanuary 20, 2026
Extremities Regulatory Spine Top Stories SurGenTec® Achieves Key Milestone with Expanded Indications for OsteoFlo® HydroFiber™ byTim AllenJuly 22, 2025
Spine Top Stories SurGenTec® Launches INSITE™ Sterile Surgery-Ready Kit with Implant and Instruments for SI Joint Fusion byTim AllenJuly 15, 2025
Regulatory Top Stories SurGenTec® Breaks New Ground with FDA Clearance for OsteoFlo® HydroFiber™, Receives Indication for Stand-Alone Use Equivalent to Autograft byJosh SandbergJanuary 16, 2025
Biologics Regulatory Spine Top Stories SurGenTec Receives FDA Clearance for B-MAN Bone Marrow Aspirate Kit with Integrated Filtration byTim AllenAugust 27, 2024
Regulatory Spine Top Stories SurGenTec® Receives FDA Clearance for OsteoFlo® HydroPutty™, a Hydrophilic Synthetic Bone Graft byJosh SandbergMarch 7, 2024
Regulatory Spine Top Stories SurGenTec® Unveils TiLink™—Revolutionary Posterior Sacroiliac Fusion System Featuring Novel Compression Capability byJosh SandbergOctober 3, 2023
Regulatory Spine Top Stories SurGenTec’s TiLink-L Receives FDA Clearance, Leading the Way as the First Offering in its Advanced Sacroiliac Joint Fusion Portfolio byJosh SandbergJune 9, 2023
