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Huntsville, AL (February 12, 2024) – Curiteva, a privately held manufacturing and technology company announces the appointment of Kevin Foley, MD, to the board of directors. Dr. Foley is a distinguished neurosurgeon, chairman of the Semmes Murphey Neurologic and Spine Institute and a professor of neurosurgery, orthopedic surgery, and biomedical engineering at the University of Tennessee Health Science Center. 

Huntsville, AL based technology manufacturer Curiteva announced FDA 510(k) clearance of the Inspire 3D Printed Trabecular PEEK Lumbar Interbody Fusion System for use in anterior, transforaminal, posterior, and lateral lumbar interbody fusion procedures. This marks the company’s second FDA cleared 3D printed PEEK implant with HAFUSE, following the approval of the Inspire Trabecular PEEK Cervical Interbody Fusion System in February 2023.

Curiteva, a privately held technology and manufacturing company based in Huntsville, AL, is proud to announce the commercial launch of its Prowess Laminoplasty System. The system is designed to provide surgeons with the tools they need to perform posterior decompression of the cervical spine with greater precision, accuracy, and efficiency.

Huntsville, AL based technology company Curiteva® announces FDA 510(k) clearance to market a Navigation Instrument System to complement their Prodigy® Pedicle Screw System and SI-LUTION® Sacroiliac Joint Fusion Systems. The pioneers in 3D printed PEEK interbody fusion technology designed these instruments to integrate seamlessly with the market leading navigation system assisting surgeons in precisely locating anatomical structures for open and MIS procedures.

Curiteva, a privately held technology and manufacturing company based in Huntsville, AL announces the commercial launch of its Inspire Porous PEEK HAFUSE Cervical Interbody System.

Huntsville, AL based technology company Curiteva is pleased to announce the expansion of its patent portfolio with the issuance of the third Utility Patent in support of their novel Inspire 3D printed porous PEEK with HAFUSE technology. This marks the 16th issued patent for Curiteva strengthening their position as a market leader in the 3D printing of porous PEEK.

Curiteva announced a limited commercial release utilizing its recently FDA-cleared Inspire Porous PEEK HAFUSE Cervical Interbody System. Curiteva pioneered and received clearance of the world’s first 3D printed, fully interconnected porous PEEK structure, utilizing internally developed Fused Filament Fabrication.

BONEZONE reports that Curiteva received FDA 510(k) clearance for Inspire Porous PEEK. The cervical interbody system is manufactured through a proprietary and patented Fused Filament Fabrication (FFF) 3D printer that is designed, programmed and built by Todd Reith.

Orthopedics This Week reports on the U.S. Food and Drug Administration (FDA) granting 510(k) clearance to a truly novel 3D printed PEEK implant.