ORTHOFLASH®

SurGenTec INSITE Sterile Kit

SurGenTec Launches INSITE Sterile Surgery-Ready Kit

The INSITE kit for SI fusion features a complete set of single-use, sterile instruments paired with a 3D-printed titanium implant.

Wenzel Spine Receives FDA Clearance for First Expandable Sacroiliac Fusion Implant, panaSIa

Wenzel Spine Gains 510(k) for panaSIa Expandable SI Fusion Implant

Its expandable architecture allows the implant to pierce the ilium and sacrum, stabilizing the SI joint and enabling post-expansion graft delivery without disengaging the instrumentation.

IMPLANET and distribution partner Sanyou Medical have registered the JAZZ range, dedicated to tape fixation in the treatment of spinal pathologies, on the Chinese market.

IMPLANET JAZZ Range Approved in China

IMPLANET and distribution partner Sanyou Medical have registered the JAZZ range, dedicated to tape fixation in the treatment of spinal pathologies, on the Chinese market.

SurGenTec Launches INSITE Sterile Surgery-Ready Kit

The INSITE kit for SI fusion features a complete set of single-use, sterile instruments paired with a 3D-printed titanium implant.

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Wenzel Spine Gains 510(k) for panaSIa Expandable SI Fusion Implant

Its expandable architecture allows the implant to pierce the ilium and sacrum, stabilizing the SI joint and enabling post-expansion graft delivery without disengaging the instrumentation.

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IMPLANET JAZZ Range Approved in China

IMPLANET and distribution partner Sanyou Medical have registered the JAZZ range, dedicated to tape fixation in the treatment of spinal pathologies, on the Chinese market.

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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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