SPINEMarketGroup

FLOWOOD, Miss., Nov. 14, 2025 /PRNewswire/ -- Zavation Medical Products, LLC ("Zavation"), a leading innovator in spinal device technology, proudly announces the launch of NanoPrime™, a next-generation implant material that combines the mechanical advantages of PEEK with the biological benefits of titanium through advanced titanium … [Read More...] about Zavation Medical Products Announces NanoPrime™: A Breakthrough in PEEK and Titanium Hybrid Interbodies

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 … [Read More...] about Curiteva Proudly Announces the Publication of a Peer-Reviewed Study in the Journal of Biomaterials (JBI)

BOSTON, Nov. 12, 2025 /PRNewswire/ -- OnPoint Surgical, Inc., a leader in Augmented Reality (AR) and Artificial Intelligence (AI) guidance for spinal interventions, today announced the appointment of Jeremy Laynor as Chief Commercial Officer (CCO). Mr. Laynor brings over two decades of executive leadership experience in the medical device, software, and health technology … [Read More...] about OnPoint Surgical, Inc. Appoints Jeremy Laynor as Chief Commercial Officer to Accelerate Global Growth

GRAND RAPIDS, Mich., Nov. 13, 2025 /PRNewswire/ -- HAPPE Spine, an early stage company advancing clinical outcomes with a proprietary biomaterial and manufacturing platform for creating bone-integrating implants, announces that the INTEGRATE®-C Interbody Fusion System has been implanted in more than 1,000 patients, demonstrating clinical adoption of the HAPPE® platform across … [Read More...] about HAPPE Spine Reaches 1,000 Patients with the INTEGRATE®-C Interbody Fusion System

ALTSTÄTTEN, Switzerland and BOSTON, Nov. 13, 2025 /PRNewswire/ -- icotec, the pioneer of implantable devices made from BlackArmor® Engineered Carbon/PEEK, today announced that the U.S. Food and Drug Administration (FDA) has cleared the CMORE® CT System for use in the cervicothoracic spine. The CMORE® (CT) System is an enhanced set of instruments and … [Read More...] about icotec Receives FDA Clearance for the CMORE® CT System, Expanding its BlackArmor® Engineered Carbon/PEEK Technology to the Posterior Cervicothoracic Spine

WEST CHESTER, Pa., Nov. 13, 2025 /PRNewswire/ -- Centinel Spine®, LLC ("the Company"), the leading global medical device company focused exclusively on treating cervical and lumbar spinal disease with the most complete and clinically-proven total disc replacement (TDR) technology platform in the world (prodisc®), today announced that more than 300,000 prodisc devices have now … [Read More...] about Centinel Spine® Surpasses 300,000 prodisc® Implantations, Reinforcing Its Leadership in Total Disc Replacement

SHELTON, Conn., Nov. 13, 2025 (GLOBE NEWSWIRE) -- Spine Wave is pleased to announce the initial surgical procedures benefiting from Spine Wave’s Testa™ TP Pivoting Spacer System featuring TiCell® Nano Advanced Surface Technology. These initial procedures were performed by Alexander R. Vaccaro, M.D., Ph.D., MBA¹ of Rothman Orthopaedics at Jefferson Health, Philadelphia, PA., and Paul C. Celestre, … [Read More...] about Spine Wave Announces Initial Surgical Procedures with the Testa™ TP Pivoting Spacer System featuring TiCell® Nano Advanced Surface Technology

Boston, November 13, 2025: IMPLANET (Euronext Growth: ALIMP, FR0013470168, eligible for PEA-PME), a medical technology company specializing in implants for orthopedic surgery and the distribution of advanced medical equipment, today announced the signing of a partnership agreement with 8i Robotics Inc. The first milestone of this agreement focuses on clinical research aimed at … [Read More...] about IMPLANET signs partnership agreement with 8i Robotics Inc. for the clinical evaluation of a surgeon-supervised robotic system for spine surgery

Eminent Spine's 3D Printed Titanium posterior SI system compresses and transfixes the SI joint. Plano, TX, November 12, 2025 --(PR.com)-- Eminent Spine, a leader in spinal implant innovation, proudly announces that its revolutionary 3D Printed Titanium Posterior SI System has received FDA 510(k) clearance as of October 7, 2025. Innovative Design & Superior EngineeringThe 3D Printed … [Read More...] about Eminent Spine’s 3D Printed Titanium Posterior SI System Receives FDA 510(k) Clearance

Today’s facilities demand enabling technologies that integrate seamlessly into existing workflows without driving up costs or requiring new infrastructure. The WatchTower Spine Navigation System was designed around this philosophy: simple setup, familiar imaging, and precise guidance without workflow disruption. JUPITER, FL – November 2025 — In an era when technology is rapidly reshaping spine … [Read More...] about Captiva Spine Announces FDA Clearance for Flat-Panel C-Arm Image Calibrators and AI-Assisted Registration for WatchTower Spine Navigation, Advancing Efficiency, Radiation Reduction, and Future-Ready Access

LOS ANGELES-- NavJam LLC today announced an exclusive worldwide sales and distribution agreement granting Ruthless LLC, doing business as Ruthless Spine, the rights to market NavJam’s patented and patent-pending spinal surgery instruments. The agreement covers NavJam’s patented “smart” Jamshidi and its upcoming KS Drill Guide for power drills, which are designed to work in tandem with Ruthless … [Read More...] about NavJam LLC Announces Exclusive Global Distribution Partnership with Ruthless Spine

LISLE, Ill., Nov. 12, 2025 /PRNewswire/ -- Hubly Surgical today announced FDA 510(k) clearance expanding Hubly Auto-Stop Drill indications to include spinal decompression procedures. To date, many thousands of neurosurgical patient lives have been saved using Hubly Auto-Stop Drills; the device's SMART auto-stop halts rotation and prevents forward plunge at the instant of skull … [Read More...] about Hubly Surgical Auto-Stop Drill Receives FDA 510(k) Clearance for Spinal Decompression Surgery: Laminectomy and Laminotomy

By integrating intraoperative data from Proprio's Paradigm™ platform with the Harms Study Group registry, the partnership ushers in a new era of quantitative, AI-enabled spine surgery research SEATTLE, Nov. 12, 2025 /PRNewswire/ -- Proprio, the surgical technology company pioneering AI-powered surgical intelligence, today announced a partnership with the Harms Study Group … [Read More...] about Proprio and Harms Study Group Partner to Advance AI-Powered Research in Spine Surgery