Jeffrey Mullin, MD, from University of Buffalo Neurosurgery shared his experience, stating “After using the Inspire Technology for the past two years in my high-risk patients, I’ve seen firsthand the rapid bone growth through and around the fusion construct, all without seeing any cases of pseudarthrosis or cage subsidence. This milestone is not only a celebration of the patients’ lives impacted but, it’s likely just the beginning of rapid market adoption given the exceptional outcomes when using the Inspire technology”.
Eric Linder, Curiteva’s Co-Founder and Chief Technology Officer, highlighted the importance of this designation stating, “The FDA’s acknowledgment of our nanotechnology claim provides additional validation of our innovative design, confirming compliance with the agency’s guidelines for nanotechnology-based materials and reinforcing the Inspire technology as a pioneering solution within the medical implant sector.”
Dr. Randy Dryer, Curiteva’s CMO, was the first to implant the device. “Bringing the Inspire Standalone ALIF across the finish line and into the operating room is a significant accomplishment,” states Dr. Dryer following the procedure. “As we have seen with this technology, the visual verification of bone growth through the implant, paired with outstanding clinical results, aligns perfectly with what surgeons are seeking. I’m confident this implant will define a new standard for standalone ALIF procedures, delivering a best-in-class solution designed to enhance patient outcomes. I’m excited to incorporate this approach to my Inspire armamentarium.”
HUNTSVILLE, Ala., November 13, 2025 (Newswire.com) – Curiteva, Inc. a privately held manufacturing and technology company, proudly announces the publication of a peer-reviewed study, “Novel PEEK fabrication using fused strand deposition reduces inflammation and enhances MSC differentiation promoting bone growth and implant osseointegration,” in the Journal of Biomaterials (JBI). JBI is one of the most highly regarded and highest-impact journals in the biomaterials and materials science fields.
The Inspire portfolio builds upon its proven success, with more than 7,300 Inspire Interbodies already implanted across four product lines; Cervical, lumbar PLIF, lumbar TLIF and lumbar ALIF. Data underscores its efficacy, showcasing consistent evidence of both on-growth and through-growth throughout the implant’s structure, elevating the standard of patient care.
Dr. Stephen Tolhurst from Texas Back Institute noted, “I’ve been using the Inspire with HAFUSE technology for over two years. The results I am seeing and the timeframe in which they are achieved is striking. The implant design and cage technology are truly unique and allow for visual confirmation of bone growth both on and through the implant. I’m excited to bring the newly cleared Inspire Trabecular PEEK Standalone ALIF System into my practice and look forward to the positive impact it will have on patient outcomes.”
HUNTSVILLE, Ala., May 6, 2025 (Newswire.com) – Curiteva, a leader in 3D-printed Trabecular PEEK implant technology, is pleased to announce an expanded partnership with Promimic, pioneers in nanotechnology, delivering advanced implant solutions with unmatched capabilities. The partnership combines Promimic’s groundbreaking surface modification with Curiteva’s innovative Inspire® technology, establishing a new benchmark in the medical device industry.
HUNTSVILLE, Ala., April 15, 2025 (Newswire.com) – Curiteva, Inc., a pioneering technology and manufacturing company, is pleased to announce a significant achievement with over 5,000 levels successfully treated using the Inspire Cervical implant, just two years after its first surgical use in April 2023. This milestone highlights the continued adoption of the novel 3D printed trabecular PEEK implant, further establishing Curiteva’s presence as a leader in spine innovation.
Huntsville, AL., (December 3, 2024) – Curiteva, Inc., a privately held manufacturing and technology company, today announced it has implanted over 2,000 patients with the Inspire®C Cervical Interbody Fusion Device. This success translates to more than 3,700 implants placed, demonstrating the system’s rapid adoption and effectiveness since its commercial launch in July 2023.
Anterior cervical discectomy and fusion (ACDF) is a common procedure for the surgical treatment of degenerative pathologies of the cervical spine. The utilization of interbody fusion implants is a well-established technique to restore disk space height, alignment, decompress the exiting nerve roots, and provide surface area for fusion of the adjacent vertebrae. Successful fusion is critical for the long-term stability and function of the cervical spine and for maintenance of the overall clinical outcome. Polyetheretherketone (PEEK) is a material commonly used for interbody fusion implants. Benefits of PEEK include radiolucency, less stress shielding compared to titanium implants and improved modulus which may provide better loading characteristic. The ability to better visualize the fusion at the osseous-implant junction is a benefit preferred by many surgeons. Click here to read the full white paper.
Corporate Headquarters
25127 Will McComb Dr.
Tanner, AL 35671
© 2023 Curiteva, Inc., All right reserved.
The PROWESS System provides a comprehensive solution for Laminoplasty procedures and consists of streamlined instrumentation and a variety of plate and spacer options for intraoperative adaptability. The instrumentation are intuitive and maintain secure connections to the implants. The implants are offered in a range of sizes and are color coded for easy visual identification.
Prowess Spacer Plates
Prowess Hook Plates
Prowess Hinge Plates
Prowess Spacers
Prowess Screws
CuriGraft® Viable Allogenic Bone Matrix is the next generation allograft containing the three key elements ideal for bone formation, offering a variety of clinical applications, including the spine, upper extremity, foot and ankle and orthopedic oncology.
| Size | Product Code |
| 1.0cc | C034-0001-MCBMV |
| 2.5cc | C034-0025- MCBMV |
| 5.0cc | C034-0005- MCBMV |
| 10.0cc | C034-0010- MCBMV |
Reference: 1) Gruskin, E. et.al., Demineralized bone matrix in bone repair: history and use. Advanced Drug Delivery Reviews, 2012. 64:1063-1077 Biologics
CuriGraft® DBM Putty is a demineralized bone putty matrix indicated for use in the extremities, posterolateral spine, and pelvis as a bone void filler or for treatment of osseous defects.
| Size | Product Code |
| 1.0cc | C024-0001-PTYV |
| 2.5cc | C024-0025-PTYV |
| 5.0cc | C024-0005-PTYV |
| 10.0cc | C024-0010-PTYV |
Reference: 1) Kiely, P.D. et al., (2014) Evaluation of a new formulation of demineralized bone matrix putty in a rabbit posterolateral spinal fusion model. The Spine Journal. September 14(9): 2155-2163.
The SI-LUTION® Sacroiliac Joint Fusion System is designed to offer immediate stability and long-term fixation across the sacroiliac (SI) joint. The implants are machined out of Titanium and incorporate the proprietary TRU-LOK® micro-textured surface technology. The cannulated system offers screws in multiple diameters and various lengths with optional static or kinetic stabilization caps to provide an ideal solution for every patient.
Key Features
Kinetic and Static
The Savant Anterior Lumbar (ALIF) Interbody Fusion System features three footprints in various heights and lordotic angles offering an ideal fit for every patient.
System Features
The Prodigy MIS Pedicle Screw System is designed to minimize the complexity of procedural steps while correcting and stabilizing the posterior thoracolumbar spine through a percutaneous approach. This system provides the same strength and rigidity as the Prodigy Polyaxial Screw System.
Key Features
Key Features
The Prodigy Polyaxial Pedicle Screw System is a posterior spinal fixation system designed to enhance the surgical experience by providing surgeons with its comprehensive implant offering and ergonomically designed instrumentation. The low-profile, friction fit design is offered in both standard and reduction geometries.
Key Features
Key Features
Key Features
Key Features
The Savant Transforaminal Lumbar (TLIF) Interbody Fusion System is offered in three different material types, multiple footprints, heights, and lordosis providing multiple options for the surgeon. The convex design offers a more accurate fit to the patient’s anatomy and offers oversized, central lateral graft windows for biologic seeding. The Savant Interbody Fusion System offers Comprehensive discectomy instruments and features instrumentation that allows for better control and more precise implant placement.
Key Features
Key Features
Key Features
The Savant Posterior Lumbar (PLIF) Interbody Fusion System self-distracting, bulleted tip is offered in three different material types, multiple footprints, heights, and lordosis providing multiple options for the surgeon. The Savant PLIF Interbody Fusion System features instruments that are simple and intuitive to use.
The Aptitude Cervical Plates feature a slim profile design allowing for a smooth anterior service. The simple and intuitive one-step locking mechanism facilitates complete control by the surgeon during the procedure. The Aptitude system offers streamlined instrumentation to accommodate the needs of the patients and surgeons.
Same screws used for both Standard and Midline plates
The Sage Cervical Interbody Fusion System is designed to support cervical loads while maximizing surface between the implant and vertebral bodies. The Interbody is offered in four footprints to accommodate individual patient anatomy while the streamlined instrumentation is designed to aid in consistent and accurate implant placement.
Key Features
Key Features
Key Features