ORTHOFLASH®

The screw is indicated for fixation and stabilization of arthrodesis, osteotomies, fractures, and nonunion of the foot and ankle.

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.

The next-generation headset is designed to maximize comfort, balance, and wearability in the operating room.

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.

LEM Surgical Dynamis Robotic Surgical System

LEM Surgical Completes First US Clinical Procedures

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

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.

,
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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OrthoPediatrics Gains 510(k) for 3P Pediatric Plating Small-Mini System

The line features variable-angle locking implants designed specifically for pediatric patients, and supports a range of trauma and deformity surgeries.

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FDA Breakthrough Designation for Zimmer Biomet Iodine-Treated Total Hip

The iTaperloc Complete and iG7 Hip are coated with the biocompatible, essential nutrient that does not cause antibiotic resistance and is commonly used in medicine as an antiseptic.

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Aurora Spine Launches Biologics Portfolio

The companies’ 100% allograft bone products are available in fiber, DBM putty and sponge strip formats.

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