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Fixation System Articles & Analysis

17 news found

OSSIO Receives Vizient Contract for Bio-Integrative Orthopedic Fixation Technology

OSSIO Receives Vizient Contract for Bio-Integrative Orthopedic Fixation Technology

These products include sterile, disposable instrument kits: OSSIOfiber Hammertoe Fixation System – 10-degree and straight implants in 2.5mm, 2.9mm and 3.2mm sizes. ...

ByOSSIO Inc


OSSIO Awarded FDA 510(k) Clearance for OSSIOfiber Compression Screw Portfolio

OSSIO Awarded FDA 510(k) Clearance for OSSIOfiber Compression Screw Portfolio

“With compression screws being one of the most widely used fixation tools used today, OSSIO’s latest contribution to the fixation market shows real promise in successfully addressing multiple lower and upper extremity injuries. ...

ByOSSIO Inc


TISSIUM to present study results at the Hernia 2021 European Hernia Society - American Hernia Society Joint Congress

TISSIUM to present study results at the Hernia 2021 European Hernia Society - American Hernia Society Joint Congress

TISSIUM, a privately-owned medtech company developing biomorphic programmable polymers for tissue reconstruction, will present an e-poster on its research on a novel, atraumatic, and consistent hernia mesh fixation device at the Hernia 2021 European Hernia Society – American Hernia Society Joint Congress. ...

ByTISSIUM


SIGNUS and eCential Robotics announce long-term partnership offering an optimized solution combining navigation, robotics and implant systems for spine surgeries

SIGNUS and eCential Robotics announce long-term partnership offering an optimized solution combining navigation, robotics and implant systems for spine surgeries

Gières (Grenoble), France, and Alzenau, Germany, September, 28 2021 – eCential Robotics, a French growth company that designs, manufactures, and markets the first unified 2D/3D robotic imaging and surgical navigation system for bone surgery indications, and SIGNUS, an international and family-run company based in Germany that has been the experienced specialist ...

ByeCential Robotics


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

Food and Drug Administration (FDA 510k) clearance for its Photodynamic Bone Stabilization System. The new clearance allows IlluminOss to be used in femur and tibia fractures as supplemental fixation to FDA-cleared fracture fixation systems. ...

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

(www.conextionsmed.com), an innovator in tendon repair, announced today the first patient has been treated with the Coronet Soft Tissue Fixation System in a Kidner procedure. 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 ...

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 ...

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

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 polymer, contained within an expandable balloon, to create a patient-conforming, rigid implant within the bone canal. ...

ByIlluminOss Medical, Inc.


Centric Medical Announces Commercial Launch of MTP Plating System

Centric Medical Announces Commercial Launch of MTP Plating System

Centric Medical, the Foot & Ankle division of Life Spine, Inc., which focuses on developing surgical implants for the treatment of distal extremity pathology announced today the commercial launch of its MTP Plating System. This System is comprised of various plates, screws and other fixation components intended to stabilize bone ...

ByCentric Medical, LLC


Centric Medical Announces First Clinical Cases With Saturn External Fixation System

Centric Medical Announces First Clinical Cases With Saturn External Fixation System

Centric Medical, the Foot & Ankle division of Life Spine, Inc., which focuses on developing surgical implants for the treatment of distal extremity pathology announced today the first clinical cases of SATURN External Fixation System. This System is comprised of various rings, struts, pins, bolts, and other fixation ...

ByCentric Medical, LLC


IlluminOss Medical Launches the IlluminOss Bone Stabilization System for Use in the Treatment of Traumatic and Fragility Fractures in the U.S.

IlluminOss Medical Launches the IlluminOss Bone Stabilization System for Use in the Treatment of Traumatic and Fragility Fractures in the U.S.

IlluminOss Medical, Inc. will be in Booth #6243 at the AAOS 2019 Annual Meeting in Las Vegas, NV from March 12-16th and will be presenting data regarding the IlluminOss System on March 13th at 1:45 pm in Exhibit Hall B at Booth #3032. “We are thrilled to announce the commercial launch of the IlluminOss System,” said Jeff Bailey, CEO, IlluminOss ...

ByIlluminOss Medical, Inc.


Centric Medical Announces 510(K) Clearance of the Saturn External Fixation System

Centric Medical Announces 510(K) Clearance of the Saturn External Fixation System

Food and Drug Administration (FDA) has given 510(k) marketing clearance to the SATURN External Fixation System which consists of rings, struts, threaded rods, pins, wires and connectors intended to be used as a means to stabilize the foot, ankle and long bone segments. “I am excited to continue the expansion of our foot and ankle portfolio with more ...

ByCentric Medical, LLC


Centric Medical Announces First Quarter Participation at Industry Meetings To Showcase Its Foot & Ankle Portfolio

Centric Medical Announces First Quarter Participation at Industry Meetings To Showcase Its Foot & Ankle Portfolio

Centric Medical will be promoting the TARSA-LINK® Stand-Alone Wedge Fixation System, the TARSA-LINK® BUNION Stand-Alone Wedge Fixation System, the ROGUE™ Hammertoe Correction System, as well as the newly FDA cleared Foot Plating System and the Cannulated Screw ...

ByCentric Medical, LLC


Centric Medical Announces FDA 510(K) Clearance of the Foot and Ankle Plating System

Centric Medical Announces FDA 510(K) Clearance of the Foot and Ankle Plating System

The Centric Medical Foot and Ankle Plating System is comprised of a variety of plates and screws intended to stabilize and fixate bone for a myriad of procedures. ...

ByCentric Medical, LLC


Wenzel Spine Announces Acquisition of Interspinous & Facet Fixation Product Platforms

Wenzel Spine Announces Acquisition of Interspinous & Facet Fixation Product Platforms

Wenzel Spine, Inc., a medical technology company focused on providing minimally invasive solutions for the treatment of spinal disorders, today announced that it has completed the acquisition of the PrimaLOK™ SP Interspinous Fusion System and PrimaLOK™ FF Facet Fixation System from OsteoMed, LLC. ...

ByWenzel Spine, Inc.


Silver Bullet Therapeutics Announces CE Mark Approval for the OrthoFuzIon Cannulated Bone Screw System

Silver Bullet Therapeutics Announces CE Mark Approval for the OrthoFuzIon Cannulated Bone Screw System

Silver Bullet Therapeutics, Inc., a privately-held medical device company, announced today that it has received CE Mark approval for the commercial sale of its antimicrobial OrthoFuzIon Cannulated Bone Screw System for orthopedic reduction and internal fixation (ORIF) procedures in the European Union. ...

BySilver Bullet Therapeutics, Inc.


ASTM F1541 - 02(2011) standard specification and test methods for external skeletal fixation devices

ASTM F1541 - 02(2011) standard specification and test methods for external skeletal fixation devices

It is anticipated that a companion testing standard using this classification system will subsequently be developed. 1. Scope 1.1 This specification provides a characterization of the design and mechanical function of external skeletal fixation devices (ESFDs), test methods for characterization of ESFD mechanical properties, and ...

ByASTM International

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