May 2026 SpineCraft received U.S. FDA 510(k) clearance for its ORIO-3D Trabecular Interbody Platform, a comprehensive portfolio of 3D-printed titanium interbody implants supporting multiple spinal fusion approaches. The implants feature a biomimetic porous architecture intended to enhance osseointegration and early fixation.
March 2026 SpinePoint LLC received U.S. FDA 510(k) clearance for the Flex-Z™ Cervical Cage, the first implant in its ultra-low stiffness cushioning interbody platform. The 3D-printed porous titanium cervical interbody implant is designed to improve load distribution and promote fusion in anterior cervical procedures.
March 2026 IMPLANET received U.S. FDA 510(k) clearance for its Swingo™ 3D Cage Range, a portfolio of 3D-printed titanium interbody fusion cages designed for multiple spinal surgical approaches. The system expands the company's interbody implant portfolio in the U.S. market.
January 2026 Spine Innovation LLC received U.S. FDA 510(k) clearance for the LOGIC™ Titanium Expandable Interbody System. The expandable titanium implant is intended for lumbar interbody fusion procedures and features a 3D-printed porous structure to promote osseointegration and spinal stability.