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Bone Implant Articles & Analysis

29 news found

CELLINK and Ossiform Enter a Strategic Partnership to launch Ossi Ink, a printable bioink based on Ossiform’s P3D Bone material

CELLINK and Ossiform Enter a Strategic Partnership to launch Ossi Ink, a printable bioink based on Ossiform’s P3D Bone material

While the advent of personalized bone implants provides a treatment pathway that can drastically improve the quality of life for many of these patients. ...

ByCELLINK


gammaCore Sapphire Non-Invasive Vagus Nerve Stimulator (nVNS) Receives Unique National Product Code Number by the Belgian Pharmaceutical Association

gammaCore Sapphire Non-Invasive Vagus Nerve Stimulator (nVNS) Receives Unique National Product Code Number by the Belgian Pharmaceutical Association

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another ...

ByelectroCore, Inc.


electroCore, Inc. Announces Distribution Agreement with Joerns Healthcare, LLC

electroCore, Inc. Announces Distribution Agreement with Joerns Healthcare, LLC

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another ...

ByelectroCore, Inc.


gammaCore Non-Invasive Vagus Nerve Stimulation (nVNS) Improves Neurobehavioral Outcomes in a Model of Traumatic Brain Injury

gammaCore Non-Invasive Vagus Nerve Stimulation (nVNS) Improves Neurobehavioral Outcomes in a Model of Traumatic Brain Injury

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another ...

ByelectroCore, Inc.


RevBio Receives Approval from the U.K.’s Regulatory Authority to Initiate a Clinical Trial for an Optimized Formulation of its Dental Bone Adhesive Biomaterial

RevBio Receives Approval from the U.K.’s Regulatory Authority to Initiate a Clinical Trial for an Optimized Formulation of its Dental Bone Adhesive Biomaterial

RevBio, Inc., announced that it has received approval from the Medicines and Healthcare products Regulatory Agency in the United Kingdom to start a 15-patient clinical trial to examine the safety and efficacy of immediately stabilized dental implants following tooth extractions using an optimized formulation of Tetranite®, the company’s bone adhesive ...

ByRevBio Inc.


gammaCore (Non-Invasive Vagus Nerve Stimulation; nVNS) Reduces Symptoms of Acute Withdrawal in Patients with Opioid Use Disorder

gammaCore (Non-Invasive Vagus Nerve Stimulation; nVNS) Reduces Symptoms of Acute Withdrawal in Patients with Opioid Use Disorder

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another ...

ByelectroCore, Inc.


electroCore, Inc. Announces Study of gammaCore Sapphire for the Treatment of Post-COVID Syndrome

electroCore, Inc. Announces Study of gammaCore Sapphire for the Treatment of Post-COVID Syndrome

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another ...

ByelectroCore, Inc.


electroCore, Inc. Announces gammaCore Non-Invasive Vagus Nerve Stimulator Available Through National Spine and Pain Centers

electroCore, Inc. Announces gammaCore Non-Invasive Vagus Nerve Stimulator Available Through National Spine and Pain Centers

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another ...

ByelectroCore, Inc.


Catalyst OrthoScience Announces Todd Wilson, PhD as Vice President of Medical Education and Training

Catalyst OrthoScience Announces Todd Wilson, PhD as Vice President of Medical Education and Training

The Archer™ CSR Total Shoulder System is unique, offering precision and accuracy in shoulder restoration while preserving the patient’s bone and soft tissue. The Archer™ R1 Reverse Shoulder System is a single-tray arthroplasty system that offers surgeon-targeted implant positioning, a streamlined and versatile system, and bone ...

ByCatalyst OrthoScience Inc.


Catalyst OrthoScience Announces David Sharp as Vice President of Global Marketing

Catalyst OrthoScience Announces David Sharp as Vice President of Global Marketing

The Archer™ CSR Total Shoulder System is unique, offering precision and accuracy in shoulder restoration while preserving the patient’s bone and soft tissue. The Archer™ R1 Reverse Shoulder System is a single-tray arthroplasty system that offers surgeon-targeted implant positioning, a streamlined and versatile system, and bone ...

ByCatalyst OrthoScience Inc.


Catalyst OrthoScience Features Innovative Products And Shoulder Surgery Leaders At AAOS

Catalyst OrthoScience Features Innovative Products And Shoulder Surgery Leaders At AAOS

The Archer CSR Total Shoulder System is unique, offering precision and accuracy in shoulder restoration while preserving the patient’s bone and soft tissue. The Archer R1 Reverse Shoulder System is a single-tray arthroplasty system that offers surgeon-targeted implant positioning, a streamlined and versatile system, and bone sparing ...

ByCatalyst OrthoScience Inc.


Shoulder Innovations Announces FDA Clearance of New InSet Stemless Humeral Implant

Shoulder Innovations Announces FDA Clearance of New InSet Stemless Humeral Implant

The unique design for the humeral preparation allows for the least amount of bone removal while the implant’s curved fin design maximizes axial and rotational fixation surface area. ...

ByShoulder Innovations


Scottish medical device business completes oversubscribed funding round

Scottish medical device business completes oversubscribed funding round

In addition, a new orthopaedic device which is the creation of Alan Johnstone, a Consultant Orthopaedic Surgeon at Aberdeen Royal Infirmary, is being refined by Clear Surgical for optimum implant placement and corrective bone alignment surgery. A significant reduction of time spent in surgery, with consequent cost savings, is facilitated by the OpLight ...

ByClear Surgical


IlluminOss Medical Receives FDA Clearance for Use in Femur and Tibia Fractures as a Supplement to Approved Hardware

IlluminOss Medical Receives FDA Clearance for Use in Femur and Tibia Fractures as a Supplement to Approved Hardware

Surgeons can now securely affix their hardware anywhere along the length of the IlluminOss implant.” The IlluminOss System is a minimally invasive approach for fracture repair and stabilization through a patient-conforming intramedullary implant. The system utilizes a light-curable liquid monomer, contained within an expandable balloon, to create a ...

ByIlluminOss Medical, Inc.


CoNextions Inc. Announces First Patient Treated with Coronet Soft Tissue Fixation System, a Revolutionary Tenodesis Product

CoNextions Inc. Announces First Patient Treated with Coronet Soft Tissue Fixation System, a Revolutionary Tenodesis Product

The Kidner procedure is the most common surgical treatment for a painful accessory navicular bone that causes foot/tendon pain. The Coronet Soft Tissue Fixation Systems is a tenodesis device intended for the fixation of soft tissue and tendon to bone. During the Kidner procedure a surgeon detaches the posterior tibial tendon from the bone and ...

ByCoNextions Inc.


IlluminOss Medical Receives FDA Clearance for Use in Fibula Fractures

IlluminOss Medical Receives FDA Clearance for Use in Fibula Fractures

Food and Drug Administration (FDA 510k) clearance for its Photodynamic Bone Stabilization System for treatment of fractures of the fibula. The IlluminOss System is a minimally invasive approach for fracture repair and stabilization through a patient-specific intramedullary implant. The system utilizes a light-curable liquid monomer, contained within an ...

ByIlluminOss Medical, Inc.


IlluminOss Medical Receives FDA Clearance for Expanded Clinical Use for Pelvic, Clavicle and Small-Bone Fractures

IlluminOss Medical Receives FDA Clearance for Expanded Clinical Use for Pelvic, Clavicle and Small-Bone Fractures

Food and Drug Administration (FDA 510k) clearance for its Photodynamic Bone Stabilization System for treatment of fractures of the pelvis, clavicle, and the small bones of the hands and feet: metacarpals, metatarsals, and phalanges. The IlluminOss System is a minimally invasive approach for fracture repair and stabilization through a patient-specific ...

ByIlluminOss Medical, Inc.


HealthpointCapital Acquires Majority Stake in IlluminOss Medical, Inc.

HealthpointCapital Acquires Majority Stake in IlluminOss Medical, Inc.

IlluminOss offers a unique and disruptive technology for the orthopedic trauma market. The Company's Photodynamic Bone Stabilization System is a minimally invasive approach for fracture repair and stabilization through a patient-specific intramedullary implant. The system utilizes a light-curable liquid polymer, contained within an expandable balloon, to create a ...

ByIlluminOss Medical, Inc.


CoNextions Inc. Announces FDA 510(k) Clearance of Coronet System, a Revolutionary Tenodesis Product

CoNextions Inc. Announces FDA 510(k) Clearance of Coronet System, a Revolutionary Tenodesis Product

Food and Drug Administration (FDA) for CoronetTM System, a tenodesis product intended for the fixation of tissue to bone and tissue to tissue. The Coronet’s novel design improves the soft tissue fixation strength of these repairs compared to conventional suture repairs. A streamlined delivery system allows for the simultaneous placement of the implant in ...

ByCoNextions Inc.


Additive Implants Announces FDA Clearance for SureMAX-X Cervical Spacer

Additive Implants Announces FDA Clearance for SureMAX-X Cervical Spacer

This 3D printed titanium spacer has a unique patented* design to create uniform end plate coverage and optimize load distribution. “Maximizing implant coverage of the endplates and providing for more uniform load distribution is important to minimizing implant subsidence. ...

ByAdditive Implants LLC

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