ORTHOFLASH®

HyperFlex Medical Bunion Correction

First Case in Clinical Evaluation of HyperFlex Bunion Correction

HyperFlex Bunion Correction is designed for early intervention, aiming to reduce pain, accelerate recovery and lower complication risk.

SutureTech Announces FDA 510(k) Clearance for RapidFix

SutureTech Gains FDA 510(k) Clearance for RapidFix

Cleared by FDA as the All-Suture Dual Anchor System, RapidFix is intended for fixation of soft tissue to bone in a variety of orthopedic procedures.

BONESUPPORT Cerament G Bone Graft Substitute

BONESUPPORT’s Cerament Demonstrates Strong Results in Trauma Cases

At follow-up after 11 months, treatment success, defined as complete regression of infection without recurrence, was observed in 96.1% of patients.

First Case in Clinical Evaluation of HyperFlex Bunion Correction

HyperFlex Bunion Correction is designed for early intervention, aiming to reduce pain, accelerate recovery and lower complication risk.

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SutureTech Gains FDA 510(k) Clearance for RapidFix

Cleared by FDA as the All-Suture Dual Anchor System, RapidFix is intended for fixation of soft tissue to bone in a variety of orthopedic procedures.

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BONESUPPORT’s Cerament Demonstrates Strong Results in Trauma Cases

At follow-up after 11 months, treatment success, defined as complete regression of infection without recurrence, was observed in 96.1% of patients.

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Smith+Nephew Unveils Updates for REGENETEN Bioinductive Implant

New evidence and market updates highlight the clinical performance of the REGENETEN Bioinductive Implant and support its further adoption.

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Medacta Launches QuickStitch Inside-Out Suture Placement Device

QuickStitch is an intuitive, reliable and user-friendly device engineered for precise suture placement in meniscal Inside-Out tissue repair.

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Pilot Study Results: Nexus Spine’s Tranquil Interbody Implants

Results of this study suggest that Nexus Spine’s patented technology may yield a significant improvement over competing devices.

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OrthoPediatrics Completes First Procedures with VerteGlide

Initial U.S. surgical procedures are complete using the VerteGlide Spinal Growth Guidance System to treat Early Onset Scoliosis.

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Medline UNITE Launching Achilles Repair Systems

Introduction of the FORCECORD and DEXLOCK Achilles Kits expands the company’s foot and ankle sports medicine portfolio.

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Stryker Launches Incompass Total Ankle System

Incompass was developed to mimic Stryker’s Infinity and Inbone with a similar implant profile, fixation and sulcus articulation.

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Exactech Unveils Large-Scale CT Radiomic Analysis of Shoulder Bones and Muscles

Researchers employed AI to analyze pre-op CT images and clinical outcomes from 4,000+ patients treated with Exactech’s Equinoxe shoulder.

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First Surgery with Interwedge Standalone Lateral Implant

Foundation Surgical’s Interwedge is designed to provide surgeons with a versatile standalone option for lateral interbody fusion procedures.

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NovaBone Debuts Bioactive Pre-contoured Wedge

The Bioactive Pre-contoured Wedge is the first fully-synthetic, porous bioactive glass solution to come to market and is specifically designed with osteostimulation in mind.

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University of Utah Unveils Dynamic Compression Implant

The platform technology includes bone screws, intramedullary fixation devices, and hybrid devices that address a broad range of orthopedic surgical indications.

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aap Completes Clinical Trial for Antibacterial Surface Technology

The aim of the human clinical trial is to approve antibacterial plates and screws for the treatment of ankle fractures.

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Locate Bio Expands RESTORE Clinical Study to the US

LDGraft is an investigational bone graft substitute that encapsulates, rather than surface attaches, recombinant human Bone Morphogenetic Protein-2.

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