BOCA RATON, Fla., Aug. 25, 2026 /PRNewswire/ -- Amplio Spine announced today that Nomen Azeem, MD, FAAPMR has joined the company as Chief Clinical Officer and Founding Chair of the Advisory Board. Dr. Azeem brings 15 years of clinical leadership in interventional spine and pain medicine, with experience in research oversight, clinical … [Read more...] about Amplio Spine™ Appoints Nomen Azeem, MD, as Chief Clinical Officer and Founding Chair of the Clinical Advisory Board
DeGen Medical Issues Statement on New CMS FY2027 Inpatient Classification for Patient-Specific Lumbar Fusion Procedures
Florence, SC, Aug. 25, 2026 (GLOBE NEWSWIRE) -- DeGen Medical, Inc., a U.S.-based medical device manufacturer specializing in patient-specific spinal implants, today issued a statement regarding the new FY2027 Centers for Medicare & Medicaid Services (CMS) inpatient classification for custom-made, anatomically and virtually designed interbody fusion devices and what … [Read more...] about DeGen Medical Issues Statement on New CMS FY2027 Inpatient Classification for Patient-Specific Lumbar Fusion Procedures
SpineGuard Obtains a New U.S. Patent for Its Innovative Ultrasound Technology Designed to Determine the Entry Point and Pedicular Drilling Trajectory
PARIS, August 24, 2026 – 6:00 p.m. CEST - SpineGuard (FR0011464452 - ALSGD), an innovative company that deploys its digital surgical guidance (DSG®) technology—which measures the electrical conductivity of tissues locally in real time—to ensure the safe and simplified placement of bone implants, announced today that it has been granted a new U.S. patent by the USPTO … [Read more...] about SpineGuard Obtains a New U.S. Patent for Its Innovative Ultrasound Technology Designed to Determine the Entry Point and Pedicular Drilling Trajectory
CMS 2027: Who Pays for the Implant When the Surgeon Owns the ASC?
CMS released its CY2027 outpatient and ASC proposed rule on July 2. Twelve days later it released the CY2027 physician fee schedule. The comment windows close on different dates — August 31 for the outpatient rule, September 14 for the physician rule — and most of the trade coverage has handled them as two separate stories, one about facilities and one about physicians. Read … [Read more...] about CMS 2027: Who Pays for the Implant When the Surgeon Owns the ASC?
Posterior Cervical: The Segment Everyone Serves and Nobody Owns
Seventy systems, reimbursement falling around nine percent a year, and a patient population that keeps getting older. Posterior cervical fixation wins the demographic argument in spine and still gets treated as a checkbox. It sits behind lumbar interbody in most portfolio reviews, behind whatever the enabling-technology line item is that quarter, and the commercial teams … [Read more...] about Posterior Cervical: The Segment Everyone Serves and Nobody Owns
Spinal Elements Takes Overwatch to the Neck
The Carlsbad company stretches its fixation brand north — and rents Medtronic's navigation footprint to get there. Spinal Elements has launched Overwatch PCF, a posterior cervical fixation system, and the name matters more than the launch copy suggests. Until now Overwatch has been a thoracolumbar franchise, running from the thoracic spine down through the sacrum and into … [Read more...] about Spinal Elements Takes Overwatch to the Neck
Forty Cervical Discs, One 3% Market: The Fight to Replace Fusion
Three market reports on cervical total disc replacement will describe three different industries. One sizes the global market at $451 million in 2025, reaching $775 million by 2032. Another opens at $3.33 billion and forecasts $8.09 billion by 2030. A third bundles cervical with lumbar and lands near $600 million for both. An eightfold spread is not a difference of opinion … [Read more...] about Forty Cervical Discs, One 3% Market: The Fight to Replace Fusion
MOVE-C®
MOVE-C combines the features of a second generation disc prosthesis with the simple implantation technique of a cervical cage. The prosthesis offers physiological motion in all 6 planes including axial damping with progressive resistance to motion. Furthermore, MOVE-C is the first prosthesis with additively manufactured titanium endplates and avoids the use of PE. … [Read more...] about MOVE-C®
Triadyme C Cervical Disc
Triadyme C cervical disc represents a major development for patients who suffer from degenerative disc disease and the medical professionals who care for them. It is highly differentiated from other discs on the market due to its unique material composition, which gives it superior structural integrity, and its exclusive design, which allows for proper biomechanics. Key … [Read more...] about Triadyme C Cervical Disc
SurGenTec® Named to the 2026 Inc. 5000 List of America’s Fastest-Growing Private Companies
BOCA RATON, Fla.--(BUSINESS WIRE)--SurGenTec®, a developer of surgical technologies for spine and orthopedic procedures, today announced that it has been named to the 2026 Inc. 5000, the annual list of the fastest-growing private companies in America. The prestigious list recognizes companies that have achieved remarkable growth while driving innovation, creating jobs, and … [Read more...] about SurGenTec® Named to the 2026 Inc. 5000 List of America’s Fastest-Growing Private Companies
Spineart Announces FDA Approval of BAGUERA® C Cervical Disc
GENEVA, Aug. 11, 2026 /PRNewswire/ -- Spineart announces that the BAGUERA® C cervical disc has received FDA approval for 1 and 2 contiguous levels, expanding access in the United States to a motion-preserving solution for patients suffering from cervical disc disease. As one of Spineart's foundational technologies and a cornerstone of its cervical portfolio, … [Read more...] about Spineart Announces FDA Approval of BAGUERA® C Cervical Disc
VB Spine Completes Transaction for CT-Fluoro Technology from Augmedics
NEW YORK--(BUSINESS WIRE)--VB Spine LLC ("VB Spine"), the largest privately held spine company, today announced it has completed its acquisition of the exclusive rights to Augmedics' CT-to-fluoroscopy (CT-Fluoro) technology for spine applications and will immediately begin integrating the technology into the xvision Spine System® platform. "We are pleased to complete this … [Read more...] about VB Spine Completes Transaction for CT-Fluoro Technology from Augmedics
Elevation Spine Receives FDA 510(k) Clearance for Saber-XA™, an Expandable Anterior Lumbar Interbody Fusion (ALIF) System
MONTEREY, Calif.--(BUSINESS WIRE)--Elevation Spine announced today that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for Saber-XA™, an anterior lumbar interbody fusion (ALIF) system that combines expandable cage technology with a zero-profile, FDA-cleared anterior lumbar plate. Saber-XA expandable technology enables true intra-operative customization … [Read more...] about Elevation Spine Receives FDA 510(k) Clearance for Saber-XA™, an Expandable Anterior Lumbar Interbody Fusion (ALIF) System
HumanTech Spine Expands VENUS System With Cannulated, Fenestrated Reduction Screws
HumanTech Spine GmbH has introduced cannulated, fenestrated reduction screws for its VENUS posterior stabilization system, the first product extension announced since the company completed its initial certifications under the European Medical Device Regulation. The new implants allow guidewire-assisted screw insertion and provide implant-based reduction, broadening the range … [Read more...] about HumanTech Spine Expands VENUS System With Cannulated, Fenestrated Reduction Screws
Clinical Based Evidence of Eminent Spine’s 3D Printed Titanium Pedicle Screw
Plano, TX, July 14, 2026 --(PR.com)-- Eminent Spine, a leader in advanced 3D implant technology, releases the early clinical and implant results of the world's first FDA 510(k) approved 3D printed titanium pedicle screw. The proprietary 3D printed pedicle screw, designed and manufactured by Eminent Spine received FDA 501(k) clearance on April 28, 2025. The new novel 3D … [Read more...] about Clinical Based Evidence of Eminent Spine’s 3D Printed Titanium Pedicle Screw
Globus Medical Reports Second Quarter 2026 Results
AUDUBON, Pa., Aug. 06, 2026 (GLOBE NEWSWIRE) -- Globus Medical, Inc. (NYSE: GMED), a leading musculoskeletal technology company, today announced its financial results for the second quarter ended June 30, 2026. Second Quarter 2026: “Momentum continued into the second quarter with 6% overall revenue growth, or 9% growth excluding Nevro, … [Read more...] about Globus Medical Reports Second Quarter 2026 Results
Providence™ Medical Technology Appoints Lane Major as President & Chief Executive Officer
Appointment builds on Providence's category leadership in Total Segmental Fusion (TSF) Pleasanton, Calif. — August 6, 2026 — Providence Medical Technology, Inc., an innovator in differentiated spinal fusion technologies designed to improve patient outcomes, today announced that its Board of Directors has appointed Lane Major as President & Chief Executive Officer. Major … [Read more...] about Providence™ Medical Technology Appoints Lane Major as President & Chief Executive Officer
Orthofix Reports Second Quarter 2026 Results Reflecting Continued Operational Progress
LEWISVILLE, Texas--(BUSINESS WIRE)--Orthofix Medical Inc. (NASDAQ:OFIX), a leading global medical technology company, today reported its financial results for the second quarter ended June 30, 2026, reflecting progress toward a more focused and consistent operating model. The Company also raised its full-year 2026 guidance for both net sales and adjusted EBITDA. All pro forma … [Read more...] about Orthofix Reports Second Quarter 2026 Results Reflecting Continued Operational Progress
Neuralytix Announces Full Commercial Availability of iD3 System for Intraoperative Nerve Assessment in Spine Surgery
FRUITA, CO — August 4, 2026 — Neuralytix, LLC (www.nerve.health) today announced full commercial availability of its iD3 System, an FDA 510(k)-cleared mechanomyography (MMG) platform that gives spine surgeons real-time, objective feedback on neurophysiologic changes occurring throughout decompression surgery. The launch builds on the system's initial commercial release in … [Read more...] about Neuralytix Announces Full Commercial Availability of iD3 System for Intraoperative Nerve Assessment in Spine Surgery



















