2025

Corrigendum: This article has been updated to reflect that MARVEL™ and REFLECT™ are FDA-approved devices, correcting previous descriptions that referred to them as investigational. Author’s Note:Early-onset scoliosis (EOS) remains a complex condition, and research continues to explore more effective ways of managing it. With this article, my goal was to provide an overview … [Read more...] about Managing Early-Onset Scoliosis: Which Growth-Preserving Treatments Are Clinically Approved? Exploring Innovations and the Future of EOS Management.-Updated September 2025

On August 28, 2025, a Delaware jury ruled that Life Spine’s ProLift expandable interbody implants infringed multiple claims of a valid Globus Medical patent tied to its RISE® expandable cage platform. The panel awarded Globus roughly $9.5 million in damages — about $6 million in lost profits and $3.5 million in reasonable royalties, according to court filings and company … [Read more...] about Globus, Life Spine, and the Patent Battleground: Who Sets the Rules? Is the Courtroom the New Operating Room for Spine Innovation?

AUDUBON, Pa., Aug. 28, 2025 (GLOBE NEWSWIRE) -- Globus Medical, Inc. (NYSE: GMED), a leading musculoskeletal technology company, announced that a Delaware jury has returned a verdict in favor of Globus in its patent infringement litigation against Life Spine, Inc. The jury found that Life Spine’s Prolift family of implants … [Read more...] about Globus Medical, Inc. Secures Jury Verdict in Delaware Patent Litigation Against Life Spine, Inc.

MIAMI--(BUSINESS WIRE)--The Biedermann Medtech Group, the prominent innovator in next generation spinal and extremity implant systems and procedural solutions, today announced a strategic transformation of its U.S. operations. Biedermann will expand its focus beyond product distribution to a broader platform of integrated services and solutions designed to reshape its U.S. … [Read more...] about Biedermann Medtech Group Announces Transformation of U.S. Spine Market Approach and New Business Model

TAMPA, Fla., Aug. 27, 2025 /PRNewswire/ -- PainTEQ, a leader in minimally invasive solutions for sacroiliac (SI) joint dysfunction, today announced a majority growth recapitalization co-led by Signet Healthcare Partners and Windham Capital Partners, two U.S.-based healthcare investment firms with nearly 50 years of combined investment experience in medical technology … [Read more...] about PainTEQ Secures Majority Growth Recapitalization Co-Led by Signet Healthcare Partners & Windham Capital Partners

BETHLEHEM, PA, UNITED STATES, August 27, 2025 /EINPresswire.com/ -- In a bold move to elevate performance and accelerate innovation across the MedTech industry, the combined organization of Intech, Tyber Medical, and Resolve Surgical Technologies today announced a strategic reorganization into two distinct operational business units: • Manufacturing Solutions (‘MS BU’) – … [Read more...] about Intech, Tyber Medical, and Resolve Surgical Technologies Form Two High-Impact Business Units and Appoint New Leadership

CHICAGO--(BUSINESS WIRE)--Driving Force today announced the acquisition of the groundbreaking Vertebral Motion Analysis (VMA®) technology from Wenzel Spine, marking a pivotal step in the advancement of spinal imaging and diagnostics. The acquisition positions Driving Force VMA as the sole owner and operator of the most advanced, FDA-cleared motion imaging system for diagnosing … [Read more...] about Driving Force Acquires Vertebral Motion Analysis (VMA®) Technology from Wenzel Spine

HUNTSVILLE, Ala., August 26, 2025 (Newswire.com) - Curiteva, Inc., a leading technology and manufacturing company, proudly announces the release of the first offering from its innovative Anterior Lumbar Inspire Portfolio. This advanced platform includes implant offerings in both monolithic and stand-alone designs, complemented by a comprehensive plating system for … [Read more...] about Curiteva Launches the Inspire Anterior Lumbar Portfolio

August 22, 2025 – Altstätten, Switzerland – icotec ag, the leading medical device manufacturer of Carbon/PEEK spinal implants, announces the CE approval under the European Medical Device Regulation (MDR) to market the VADER® Pedicle System inclusive of Ø 4.5 mm pedicle screws and long Carbon/PEEK rods made from BlackArmor® and its use with Medtronic StealthStation™ navigation … [Read more...] about VADER® Pedicle System – CE Approval under MDR for Line Extension & Navigated Instruments

GALWAY, Ireland, Aug. 19, 2025 /PRNewswire -- Medtronic plc (NYSE: MDT), a global leader in healthcare technology, today announced financial results for its first quarter (Q1) of fiscal year 2026 (FY26), which ended July 25, 2025. Key Highlights "We delivered another consistent quarter of mid-single digit organic revenue growth, with broad strength from several … [Read more...] about Medtronic reports first quarter fiscal 2026 financial results

Plano, TX, August 18, 2025 --(PR.com)-- Eminent Spine announced today that its trailing twelve-month total income for the period ending June 2025 has risen by nearly 70%, underscoring the company’s strong momentum and expanding presence in the spine market. This milestone comes as the company celebrates the Alpha Launch of the world’s only FDA-approved 3D Printed Titanium … [Read more...] about Eminent Spine Reports 70% Growth in Trailing 12-Month Income and Celebrates Alpha Launch of FDA-Approved 3D Printed Titanium Pedicle Screw

BOSTON, Aug. 18, 2025 /PRNewswire/ -- Intrinsic Therapeutics, Inc., a medical technology company committed to redefining the standard of care for lumbar discectomy patients with large annular defects by reducing reoperations for reherniations by 81%* with its Barricaid Annular Closure Device, announced today the appointment of industry veterans Mike Lytle and Dave Decker as … [Read more...] about Intrinsic Therapeutics Appoints Industry Veterans Mike Lytle and Dave Decker to Lead Sales and Advance Discectomy Treatment

TORONTO, Aug. 15, 2025 /PRNewswire/ - SpinaFX Medical Inc., ("SpinaFX") a leading innovator in image-guided interventional spine care, is proud to announce that its flagship device, Triojection®, has been granted Breakthrough Device Designation by the U.S. Food and Drug Administration (FDA). This milestone acknowledges Triojection's potential to offer a highly … [Read more...] about Triojection® from SpinaFX Granted Breakthrough Device Designation by U.S. FDA for Minimally Invasive Lumbar Disc Treatment

Spinal Simplicity's IntraLink technology, an injectable treatment for symptomatic disc degeneration, has received FDA Breakthrough Device Designation—fast-tracking review and potentially enabling earlier intervention for patients. Early clinical trials showed significant, sustained pain and disability improvements in over 80% of treated patients. OVERLAND PARK, Kan., Aug. … [Read more...] about Spinal Simplicity Secures FDA Breakthrough Device Designation for IntraLink™

AUSTIN, Texas--(BUSINESS WIRE)--Wenzel Spine, Inc., a medical device company pioneering minimally invasive surgical and analytic solutions for spinal disorders, today announced completion of first cases and the U.S. limited commercial launch of its novel panaSIa™ Expandable SI Fusion System. panaSIa is the first expandable sacroiliac (SI) fusion implant cleared by the FDA and … [Read more...] about Wenzel Spine Announces Limited U.S. Commercial Launch and First Cases of its Expandable panaSIa™ SI Fusion System

Shanghai, China — The clinical approval of the Intelligent SpinePecker Miniature Spinal Surgical Robot signals a new era for robot-assisted spinal surgery in China. Built on Micromate™ robotic technology from Austria-based Interventional Systems (INS) and developed in close collaboration with China’s HICREN, the innovation represents the success of a truly international … [Read more...] about China Grants Approval to First Miniature Orthopedic Surgical Robot for Spinal Procedures: Intelligent SpinePecker