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Wright Medical Shareholder Files Suit to Halt Stryker Acquisition

A Wright Medical shareholder filed a suit against Wright, its board and Stryker, claiming that the Solicitation Statement submitted to shareholders in association with the proposed acquisition is false and misleading.

Rejoint YourKnee Receives CE Mark Approval

REJOINT received CE Mark approval for the YourKnee™ patient-specific 3D-printed total knee replacement.

CoreLink Hits Milestone of 5,000 Implants with 3D-Printed Technology

CoreLink has implanted over 5,000 3D-printed spinal devices that employ proprietary Mimetic Metal® additively-manufactured technology. 

Medicrea Announces Partnership Discussions and Proposed Capital Increase

Medicrea announced a preliminary discussion for acquisition by or partnership with U.S. spine players, as well as a proposed capital funding increase.

RTI Surgical to Become Pure-Play Spine Company with Sale of OEM Business

RTI Surgical announced a definitive agreement to sell its OEM business to Montagu Private Equity for a total of $490 million.

Embody Gains Additional Funding for ACL Repair

Embody is receiving a $2.5 million Phase II research award. Funds will support development and clinical assessment of collagen-based MICROBRACE™ ACL technology for anterior cruciate ligament repair.

Biologics4Life Secures License to Bone Tissue Regeneration Technology

Biologics4Life completed an exclusive licensing agreement to secure rights to initial technologies for bone tissue regeneration.

EnMovi Formed to Develop Wearable/Data Analytics Tool for Orthopedic Procedures

OrthoSensor and McLaren Applied formed EnMovi to expand development of MOTIONSENSE™ wearable sensor technology and ORTHOLOGIQ® data analytics for use in orthopedic patient care.

Cutting Edge Spine Gains FDA Clearance of EVOLha-DLIF

Cutting Edge Spine received FDA 510(k) clearance of the EVOL®ha-DLIF direct lateral interbody fusion system.

Silver Bullet Therapeutics Gains CE Mark for OrthoFuzIon Bone Screw

Silver Bullet Therapeutics received CE Mark approval for the OrthoFuzIon™ Bone Screw for reduction and internal fixation procedures anywhere in the body.


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