ORTHOFLASH®

Bioretec RemeOs Trauma Screw System

FDA Clears Bioretec’s RemeOs Trauma Screw

The RemeOs trauma screw aims to make traditional titanium and steel implants redundant, eliminating the need for implant removal surgery.

First Case with Stryker’s Tornier Pyrocarbon Humeral Head

First Case with Stryker’s Tornier Pyrocarbon Humeral Head

Stryker now reportedly offers the only FDA-cleared pyrocarbon bearing material option for shoulder hemiarthroplasty.

G21 SpaceFlex Acetabular Cup

G-21 Gains FDA 510(k) for SpaceFlex Acetabular Cup

The SpaceFlex Acetabular Cup rounds out G-21’s hip offering, with the SpaceFlex Hip already on the market in the U.S. since 2019.

FDA Clears Bioretec’s RemeOs Trauma Screw

The RemeOs trauma screw aims to make traditional titanium and steel implants redundant, eliminating the need for implant removal surgery.

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First Case with Stryker’s Tornier Pyrocarbon Humeral Head

Stryker now reportedly offers the only FDA-cleared pyrocarbon bearing material option for shoulder hemiarthroplasty.

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G-21 Gains FDA 510(k) for SpaceFlex Acetabular Cup

The SpaceFlex Acetabular Cup rounds out G-21’s hip offering, with the SpaceFlex Hip already on the market in the U.S. since 2019.

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FDA Clearance of CoreLink Siber Ti

The Siber Ti System offers a comprehensive portfolio of fully porous, nano surfaced, 3D-printed implants.

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Marrow Access Technologies Launches Cartilage Repair Solution for Ankle

The SmartShot marrow access device is uniquely designed to promote healing and improve access in the ankle.

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Loci Orthopaedics Granted US Patent for Thumb Base Implant

Further, the USPTO intends to grant a patent for the conversion of the design from a hemi-arthroplasty to a total arthroplasty.

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aap Receives FDA 510(k) for LOQTEQ VA Elbow Plating

The system enables flexible treatment of fractures of the distal humerus and olecranon important to the elbow function and stability.

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Study Results: Medacta MySpine Accuracy in Screw Replacement

A new clinical study demonstrates Medacta’s MySpine accuracy in screw replacement during spine revision surgery.

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NuVasive Specialized Orthopedics Expands Indications of Precice Limb Lengthening

The expanded clearance extends the clinical benefits of Precice to a wider range of patients, namely pediatrics.

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Surgalign Launches Next-gen Software for HOLO Portal Surgical Guidance

The next iteration of HOLO Portal delivers advancements based on early clinical experience and insights from leading spine surgeons in the U.S.

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Accelus Gains 510(k) Clearance of Remi Robotic Navigation

FDA has issued a 510(k) clearance to Accelus for its Remi Robotic Navigation System for use with GE OEC 9900 C-Arm fluoroscopic imaging systems.

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Geistlich Expands vallos Allograft Portfolio

With multiple sizes and configurations, the vallos allograft line allows clinicians to choose exactly what they need for each procedure.

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Woven Orthopedics Gains 510(k) for Ogmend Implant Enhancement

Ogmend is an implantable sleeve to aid screw fixation in challenging scenarios. The device will be made available in the U.S. through a staged release.

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Positive Policy Decisions for ZimVie Tether

The Tether device is now deemed “medically necessary” for the treatment of pediatric scoliosis in additional patients covered by Highmark and BCBS North Dakota.

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OssDsign Hits Commercial Milestone in France

OssDsign has reached 200 implants of its 3D-printed titanium patient-specific cranial implant in France.

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