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Fixation Medical Devices 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

OSSIO, Inc., an orthopedic fixation technology company, today announced that it has received a contract with Vizient, Inc., making the company’s portfolio of bio-integrative OSSIOfiber products available at negotiated pricing to health care providers in Vizient’s group purchasing organization (GPO) under a three-year contract starting March 1. OSSIO’s contract with Vizient ...

ByOSSIO Inc


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

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

OSSIO, Inc., an orthopedic fixation technology company, today announced that its OSSIOfiber® Compression Screw Portfolio has received 510(k) market clearance from the U.S. Food and Drug Administration (FDA) for maintenance of alignment and fixation of bone fractures, comminuted fractures, fragments, osteotomies, arthrodesis and bone grafts of the upper extremity, fibula, knee, ankle and foot ...

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. The event is scheduled to be held virtually and in-person from October 13 – ...

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 for comprehensive ...

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

IlluminOss Medical, a medical device company focused on minimally invasive orthopedic fracture repair, today announced an expanded U.S. ...

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

CoNextions Inc. (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 Systems is a tenodesis device intended for the ...

ByCoNextions Inc.


IlluminOss Medical Receives FDA Clearance for Use in Fibula Fractures

IlluminOss Medical Receives FDA Clearance for Use in Fibula Fractures

IlluminOss Medical, a medical device company focused on minimally invasive orthopedic fracture repair, today announced that it has received expanded U.S. ...

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

IlluminOss Medical, a medical device company focused on minimally invasive orthopedic fracture repair, today announced that it has received expanded U.S. ...

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 segments for indications within the foot and ankle. ...

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. ...

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., a privately held, commercialstage medical device company focused on minimally invasive orthopedic fracture repair, today announced the U.S. launch and commercial availability of the 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

Centric Medical, a division of Life Spine®, Inc., which focuses on developing surgical implants for the treatment of lower distal extremity pathology, announced today That the U.S. 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 ...

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, the Foot & Ankle division of Life Spine, Inc., which focuses on developing surgical implants for the treatment of distal extremity pathology announced today that it will be participating in the 2018 American Academy of Orthopaedic Surgeons (AAOS) Annual Meeting which will be held March 6-10 in New Orleans, Louisiana, as well as the 76th Annual 2018 American College of Foot ...

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

Centric Medical, a division of Life Spine, Inc., which focuses on developing surgical implants for the treatment of distal extremity pathology announced today the FDA 510(k) clearance of the new Foot and Ankle Plating System. This clearance offers multiple surgical solutions by Centric Medical, to be used in Foot & Ankle reconstruction procedures. The Centric Medical Foot and Ankle Plating ...

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 PrimaLOKâ„¢ SP Interspinous Fusion System and PrimaLOKâ„¢ FF Facet Fixation System from OsteoMed, LLC. The PrimaLOK SP & FF platforms include a polyaxial ...

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

A1.1.1 This classification covers the definitions of basic terms and considerations for external skeletal fixation devices (ESFDs) and the mechanical analyses thereof. A1.1.2 It is not the intent of this classification to define levels of acceptable performance or to make recommendations concerning the appropriate or preferred clinical ...

ByASTM International

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