Healio

VIDEO: Use of novel device may avoid spine fusion for adolescent idiopathic scoliosis

Please provide your email address to receive an email when new articles are posted on . A novel posterior distraction device was effective in avoiding spine fusion surgery for patients at 2-year ...
Nasdaq

Aurora Spine Announces Launch of its DEXA-L™ Anterior Lumbar Interbody Fusion Device

CARLSBAD, Calif., Sept. 17, 2025 (GLOBE NEWSWIRE) -- Aurora Spine Corporation (“Aurora Spine” or the “Company”) (TSXV: ASG) (OTCQB: ASAPF), a leader in innovative spine and interventional pain ...

Amplio Spine Acquires and Commercializes KeyLift®, an FDA-Cleared Expandable Interlaminar Stabilization System Indicated for Supplemental Fusion of the Non-Cer…

Amplio Spine today announced the close of its asset acquisition of the KeyLift® Expandable Interlaminar Stabilization System ...
Business Wire

Carlsmed Announces Favorable Medicare Reimbursement Decision for Spinal Fusions with Custom-Made Anatomically Designed Devices

CARLSBAD, Calif.--(BUSINESS WIRE)--Carlsmed, the leader in personalized spine surgery, announced today that in the Hospital Inpatient Prospective Payment System Final Rule for fiscal year 2025, the ...
News Medical

First self-powered spinal implant can transmit real-time data from inside the body

A collaboration between civil engineering and neurosurgery at the University of Pittsburgh could change how spinal fusion surgery is performed and monitored. Associate Professors Amir Alavi, Nitin ...
Becker's Spine Review

Spinal fusion isn’t forever: How ASD data reshapes conversations

While spinal fusion has long been the “gold standard,” growing long-term data on adjacent segment disease is telling a different story on the best options for patients. Four spine surgeons discuss how ...
Becker's ASC

49 Orthopedic and Spine Devices Receive FDA 510 (k) Clearance in December

The Food and Drug Administration issued 49 orthopedic- and spine-related 510(k) clearances in December, according to an FDA report. 1. NuVasive Spherx II-Mas Deformity Spinal System from NuVasive. 2.
Healio

Bioretec receives FDA breakthrough device designation for spinal interbody cage

Please provide your email address to receive an email when new articles are posted on . Bioretec received FDA breakthrough device designation for its RemeOs spinal interbody cage. The cage is designed ...
WFLA News Channel 8

Understanding spinal fusion recovery: What you need to know

According to the North American Community Hub Statistics (NCHstats), back pain affects four in every five people in the United States. The discomfort and loss of mobility that it causes result in 264 ...
The Argus on MSN

Spinal implant linked to health risks leaves woman facing surgery

There are fears that thousands of people in the UK may potentially face complex surgery to remove a spinal implant that has ...
Becker's ASC

32 Orthopedic & Spine Devices Receive FDA 510(k) Clearance in August

The Food and Drug Administration granted 32 orthopedic- and spine-related device clearances in August. 1. Lanx Spinal Fixation System from Lanx. 2. Nautilus Spinal System from Life Spine. 3. Smith & ...