ORTHOFLASH®

b-ONE Ortho MOBIO Total Knee System

First Case with MOBIO Total Knee and TMINI Robotic System

THINK Surgical gained FDA 510(k) clearance for use of b-ONE Ortho’s MOBIO with TMINI in 2024.

Nanochon ChondroGraft

Nanochon Gains Approval for Clinical Trial in Canada

Nanochon Chondrograft will be evaluated in a first in human study for use in knee cartilage restoration in eligible patients.

Dymicron Triadyme Cervical Disc

IDE Approval for Dymicron Triadyme-C Artificial Disc

The trial will compare safety and effectiveness of Triadyme-C to ACDF in the treatment of symptomatic cervical disc disease.

First Case with MOBIO Total Knee and TMINI Robotic System

THINK Surgical gained FDA 510(k) clearance for use of b-ONE Ortho’s MOBIO with TMINI in 2024.

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Nanochon Gains Approval for Clinical Trial in Canada

Nanochon Chondrograft will be evaluated in a first in human study for use in knee cartilage restoration in eligible patients.

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IDE Approval for Dymicron Triadyme-C Artificial Disc

The trial will compare safety and effectiveness of Triadyme-C to ACDF in the treatment of symptomatic cervical disc disease.

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Exactech Granted 510(k) for Scapula Reconstruction System

The system supports treatment of scapular fractures using several different techniques, including single and dual plating.

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VISIE Executes First Pin-Free Knee Bone Cuts Using Spatial Computing

VISIE’s scanning platform is completely non-invasive and employs no bone-pinned trackers, clamps or registration steps.

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First Cases with Aurora Spine’s AERO Lumbar Fusion

The novel device is designed to provide a minimally invasive option for patients suffering from facet joint-related pain or instability.

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Highridge Medical to Introduce activL Lumbar Disc

Highridge licensed U.S. rights to activL and is commencing production for the launch of its own activL lumbar disc later this year.

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First U.S. Patient Treated with Cerapedics’ PearlMatrix

Of the more than 350 spinal bone grafts in the U.S. market, Cerapedics has two of only three spinal bone grafts that have successfully gone through the PMA process.

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FDA De Novo for Fziomed Oxiplex Gel

Oxiplex is an intraoperative gel indicated as an adjunct to lumbar spinal surgery to reduce post-op leg pain and neurological symptoms.

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BEAR MOON Study of Miach Ortho BEAR Implant Completes Enrollment

The BEAR MOON study will compare the BEAR Implant to autograft bone-patellar tendon-bone anterior cruciate ligament reconstruction.

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MatOrtho Gains CE Mark for ReCerf Hip Resurfacing

Made from BIOLOX delta ceramic, ReCerf eliminates concerns associated with metal-on-metal bearings and preserves more of the patient’s natural bone.

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Waldemar LINK Earns 510(k) for CORE Shoulder System

CORE is designed to assist in the placement of the K-wire for the glenoid component during total shoulder replacement.

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CGBio Launches Novomax Fusion in Japan

The third-generation cervical spine cage utilizes BGS-7, a new bioactive glass-ceramic material, that may be more biocompatible than titanium or PEEK cages.

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OssDsign Shares Update on PROPEL Spinal Fusion Study

Results show a fusion rate of 88.4% in a highly complex patient cohort, demonstrating that Catalyst nanosynthetic bone graft shows strong performance even in challenging patient populations.

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Stryker Granted FDA Clearance for Incompass Total Ankle

Incompass incorporates Adaptis Boney Ingrowth Technology and redesigned instrumentation to support long-term fixation, surgical flexibility and streamlined workflow.

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