ORTHOFLASH®

icotec CMORE CT System

icotec Gains FDA Clearance for CMORE CT System

The CMORE CT System comprises an enhanced set of instruments and implants for posterior stabilization of the upper spine.

Centinel Spine prodisc Devices

Centinel Spine Surpasses 300,000 prodisc Implantations

The platform remains the only total disc replacement system offering multiple anatomically tailored implant solutions for both the cervical and lumbar spine.

Hubly Surgical Auto-Stop Drill Receives FDA 510(k)

Hubly Surgical Auto-Stop Drill Receives FDA 510(k)

The new clearance expands use to laminectomy and laminotomy for spinal decompression to drill through the vertebral lamina and protect patients from damage to the spinal cord.

icotec Gains FDA Clearance for CMORE CT System

The CMORE CT System comprises an enhanced set of instruments and implants for posterior stabilization of the upper spine.

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Centinel Spine Surpasses 300,000 prodisc Implantations

The platform remains the only total disc replacement system offering multiple anatomically tailored implant solutions for both the cervical and lumbar spine.

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Hubly Surgical Auto-Stop Drill Receives FDA 510(k)

The new clearance expands use to laminectomy and laminotomy for spinal decompression to drill through the vertebral lamina and protect patients from damage to the spinal cord.

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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.

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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.

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LEM Surgical Completes First US Clinical Procedures

The successful procedures demonstrated the precision and efficiency of the Dynamis platform in a live clinical setting.

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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.

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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.

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BioPoly Granted U.S. Patent Protecting Shoulder Implant

The implant design reinforces the damaged labral region with a smooth, cartilage-friendly articulating surface engineered from the company’s BioPoly material.

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Aevumed Introduces PHANTOM 3.5 and 4.5mm PEEK Suture Anchors

The PHANTOM series joins Aevumed’s portfolio of fixation solutions designed to improve patient outcomes while supporting surgeon efficiency in the operating room.

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CGBio Granted 510(k) for UniSpace TPLIF Cage

The UniSpace lumbar device was designed to be compatible with CGBio’s next-generation NOVOSIS Putty bone graft substitute.

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MedCAD’s AccuStride Fixation Plates Gain 510(k) Clearance

The system is designed to provide truly patient-specific custom solutions for revisions, deformities, arthritic conditions, and trauma-related foot and ankle injuries.

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Fziomed Launches Oxiplex Gel in the US

The synthetic, absorbable gel is for use as an adjunct in lumbar spine surgery for the reduction of leg pain and neurological symptoms.

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Xtant Medical Launches CollagenX Product

The launch further expands Xtant’s biologics product portfolio to include a surgical wound closure application.

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Snke Unveils SnkeXR Open Platform AR Glasses for Healthcare

SnkeXR was designed specifically to aid the medical technology industry with integration and adoption of AR technologies into healthcare workflows.

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