ORTHOFLASH®

Captiva Spine Watchtower Spine Navigation

Captiva Spine Gains 510(k) for Watchtower Navigation Components

The advancement includes clearance for new 21 and 31 cm Flat-Panel C-Arm Image Calibrators and AI-assisted 2D-to-3D image registration.

Spine Wave Announces Initial Surgical Procedures with the Testa TP Pivoting Spacer

Initial Procedures with the Spine Wave TP Pivoting Spacer

The Testa TP Pivoting Spacer System is a pivoting interbody device for transforaminal lumbar interbody fusion.

Avicenna.AI Launches AVI Platform For Medical Imaging AI

Avicenna.AI Launches AVI Platform For Medical Imaging AI

AVI is designed to host any imaging AI application, and will initially provide access to Avicenna’s entire CINA portfolio, including solutions for vertical compression and cervical spine fractures.

Captiva Spine Gains 510(k) for Watchtower Navigation Components

The advancement includes clearance for new 21 and 31 cm Flat-Panel C-Arm Image Calibrators and AI-assisted 2D-to-3D image registration.

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Initial Procedures with the Spine Wave TP Pivoting Spacer

The Testa TP Pivoting Spacer System is a pivoting interbody device for transforaminal lumbar interbody fusion.

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Avicenna.AI Launches AVI Platform For Medical Imaging AI

AVI is designed to host any imaging AI application, and will initially provide access to Avicenna’s entire CINA portfolio, including solutions for vertical compression and cervical spine fractures.

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HAPPE Spine Reaches 1,000 Patients with INTEGRATE-C

The Hydroxyapatite Porous Polyetheretherketone biomaterial platform acts like a biologic, due to having cancellous microporosity with hydroxyapatite embedded and exposed on all surfaces.

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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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