Companion Spine’s DIAM Receives FDA Premarket Approval
DIAM is the first posterior motion-preserving device approved in the U.S. for the treatment of primary low back pain. Dec 16, 2025
3D Systems Announces FDA 510(k) Clearance Expansion
FDA has granted 510(k) clearance expanding the indications for the VSP virtual surgical platform to include adolescents. Dec 15, 2025
FDA Grants Bioretec’s DrillPin Breakthrough Device Designation
The designation covers the RemeOs DrillPin for fixation of bone fragments in pediatric and adult patients. Dec 15, 2025
Study Shows AxioMed’s Spinal Implant Replicates Human DiscÂ
The study shows that AxioMed's VTDR reproduces native lumbar-disc biomechanics across axial compression, flexion-extension, and shear. Nov 19, 2025
Proprio and Harms Study Group Form AI Research Partnership
The partnership aims to bolster quantitative, AI-enabled spine surgery research to better treat spinal deformities. Nov 19, 2025
Pace Surgical Receives FDA 510(k) Clearance for Screw System
The screw is indicated for fixation and stabilization of arthrodesis, osteotomies, fractures, and nonunion of the foot and ankle. Nov 12, 2025
Augmedics Announces FDA Clearance For Next-Gen AR Headset
The next-generation headset is designed to maximize comfort, balance, and wearability in the operating room. Nov 12, 2025
LEM Surgical Completes First US Clinical Procedures
The successful procedures demonstrated the precision and efficiency of the Dynamis platform in a live clinical setting. Nov 12, 2025
New Study Confirms Effectiveness of OrtoWay’s OrtoWell System
The study confirms the safety, usability, and intraoperative performance of the device across 30 patients treated in Germany. Nov 12, 2025
Meduloc Gains 510(k) Clearance for Fracture Fixation System
The system offers a differentiated approach, combining a strong, flexible nitinol implant with a deployable prong locking mechanism. Nov 12, 2025
