Social Media Ideas for Limiflex Dynamic Sagittal Tether

Empirical Spine Announces First Commercial LimiFlex(R) Cases at Stanford Medicine, Marking U.S. Launch of Motion-Preserv...

Empirical Spine announces the U.S. market introduction of the LimiFlex Dynamic Sagittal Tetherâ„¢, an outpatient, motion-preserving alternative to spinal fusion following decompres...

Empirical Spine Announces First Commercial LimiFlex(R) Cases at Stanford Medicine, Marking U.S. Launch of Motion-Preserv...

Empirical Spine Announces First Commercial LimiFlex(R) Cases at Stanford Medicine, Marking U.S. Launch of Motion-Preserv...

First U.S. commercial cases establish LimiFlex as an outpatient, motion-preserving stabilization option SAN CARLOS, CA / ACCESS Newswire /…

Enovis Launches Spinamic® Hybrid Scoliosis Brace, Combining Corrective Performance with Improved Wearability for Childre...

The DonJoy Spinamic® Hybrid Scoliosis Brace is a first-of-its-kind device that integrates rigid corrective elements into a breathable, adjustable design to improve both clinical ou...

Amplio Spine Acquires and Commercializes KeyLiftВ®, an FDA-Cleared Expandable Interlaminar Stabilization System Indicate...

Amplio SpineВ announced the close of its asset acquisition of theВ KeyLiftВ® Expandable Interlaminar Stabilization SystemВ from FloSpine, LLC, and the simultaneous launch of nation...

SIGNUS USA® Marks Major Milestone with First U.S. Surgery Using VertaConnect® Expandable Lumbar Spine Implant

Amplify Surgical and Emory Healthcare Complete World’s First Continuously Navigated Endoscopic TLIF Using dualPort...

Life Spine Receives FDA 510(k) Clearance for VersaLiftв„ў Expandable Interbody System Featuring a 6mm Starting Height

Life Spine, Inc. announced that it has received FDA 510(k) clearance for the VersaLiftв„ў Expandable Interbody System for TLIF and PLIF procedures featuring a low 6mm starting heig...

Amplify Surgical and Emory Healthcare Complete World’s First Continuously Navigated Endoscopic TLIF Using dualPortal &am...

Amplify Surgical announced the successful completion of what is believed to be the world’s first continuously navigated endoscopic TLIF procedure, performed at Emory Healthcare.

SurGenTec® Receives FDA Clearance for ION-L™, a Novel Lumbar Facet Fixation System Representing a Paradigm Shift in M...

SurGenTec® today announced FDA clearance of its ION-L™ Lumbar Facet Fixation System. ION-L™, indicated for the treatment of patients with (DDD) from L3 to S1 in skeletally mat...

Amplio Spine Acquires and Commercializes KeyLift®, an FDA-Cleared Expandable Interlaminar Stabilization System Indicated...

Founder-led Amplio Spine, LLC enters national commercialization following its asset acquisition of KeyLift® from FloSpine, LLC — an…

Amber Implants Advances Pivotal European EXPAND Study of VCFixВ® Spinal System in Standalone Vertebral Reconstruction

Amber Implants announced the advancement of its pivotal EXPAND clinical study evaluating the VCFixВ® Spinal System in defined patients with vertebral compression fractures.

French orthopedic pioneer Movmedix enters the United States following FDA clearance of LARSВ® Technology

As ligament injuries continue to rise among athletes and active populations, Movmedix brings more than three decades of French innovation to American surgeons.

Life Spine Receives FDA 510(k) Clearance for VersaLift™ Expandable Interbody System Featuring a 6mm Starting Height

HUNTLEY, Ill., June 23, 2026 -(BUSINESS WIRE)- Life Spine, Inc., a medical device company that designs, develops, manufactures,…

PainTEQ Launches TRAQâ„¢, A Next-Generation Posterior Approach to SI Joint Fusion

PainTEQ announced the U.S. commercial launch of TRAQ™ SI Joint Fusion — the first posterior SI joint implant designed for bi-cortical fixation through a 1-inch incision.

ACL Reconstruction for Cervical Spine Levels C1-C2?

Really fascinating new study that suggests ligament reconstruction between C1-C2 for transverse atlantal ligament rupture, not fusion.

SpinaFX Medical receives FDA Investigational Device Exemption (IDE) for Triojection®, its Breakthrough, Minimally-Invasi...

SpinaFX Medical's prospective, randomized, multicenter trial will compare intradiscal ozone/oxygen injection plus nerve root block to nerve root block alone in 300 patients in up t...

Spring Distraction Systemв„ў Reaches Its First U.S. Patient at Scottish Rite for Children

FDA-cleared, growth-friendly spinal implant developed in the Netherlands marks its U.S. clinical debut in a child with early-onset…

PainTEQ Launches TRAQв„ў, A Next-Generation Posterior Approach to SI Joint Fusion

MTF Biologics Expands FlexHD® Reconstructive Surgery Portfolio With Launch of FlexHD® Meshed

MTF Biologics has expanded its reconstructive surgery portfolio with FlexHDВ® Meshed, a pre-meshed acellular dermal allograft developed in…

SurGenTec® Receives FDA Clearance for ION-L™, a Novel Lumbar Facet Fixation System Representing a Paradigm Shift in M...

BOCA RATON, Fla., June 15, 2026 /OrthoSpineNews/ – SurGenTec®, a medical device company focused on advancing treatment options…

SIGNUS USA® Marks Major Milestone with First U.S. Surgery Using VertaConnect® Expandable Lumbar Spine Implant

NEW YORK CITY, NY, July 15, 2026 /EINPresswire.com/ — SIGNUS USA today announced the successful completion of the first surgery…

Treace Announces First Surgical Case with the HyperPlateв„ў XM Dynamic Compression Locking Implant System

Treace Medical Concept announced the successful completion of the first case utilizing its HyperPlateв„ў XM Dynamic Compression Locking Implant.

Precision SpineВ® Launches ReformВ® Ti FS Modular Fenestrated Screw System

PARSIPPANY, N.J.,В June 3, 2026В /PRNewswire/ — Precision Spine, Inc., a medical device company dedicated to Made-in-the-USA manufacturing, announced the…