Integra Enters Agreement to Develop a Short Stem and Stemless Shoulder System
Integra LifeSciences entered into a license and development agreement with Consortium of Focused Orthopedists for a short stem and stemless shoulder. Jan 08, 2019
Spineology Duo LIF Commercial and Postmarket Update
Spineology surpassed completion of 125 lateral interbody fusion cases with the Duo system. Jan 08, 2019
DiscGenics’ IDCT Passes Initial Safety Review in Phase I/II Trial
DiscGenics' injectable disc cell therapy passed an initial planned safety review of its Phase I/II trial for the treatment of mild to moderate degenerative disc disease. Jan 07, 2019
LimaCorporate and HSS Founding Hospital-Based 3D Printing Facility
LimaCorporate and the Hospital for Special Surgery are co-founding an additive manufacturing 3D printing facility to create custom orthopaedic implants in a hospital setting. Jan 07, 2019
OrthoPediatrics Expands Direct Sales in Belgium, the Netherlands
OrthoPediatrics updated an agreement with Hospithera to act as its exclusive sales agency in Belgium and the Netherlands. Jan 07, 2019
SpineEx Withdraws $17MM IPO
SpineEx, developer of an expandable device for minimally invasive lateral lumbar interbody fusion, withdrew its plans for a US $17MM initial public offering late in 4Q18. Jan 07, 2019
Episurf Medical Gains Another US Patent
Episurf Medical received another Notice of Allowance from the USPTO, addressing image segmentation used for 3D joint damage visualization as well as the design of patient-specific implants and instruments. Jan 03, 2019
Histogenics to Explore Strategic Alternatives for NeoCart Cartilage Treatment
Histogenics plans to evaluate the range of potential strategic alternatives for its NeoCart® cell therapy following FDA's indication that an additional clinical trial would be required before acceptance of a Biologics License Application submission. Jan 03, 2019
JointPoint Gains Clearance for Digital Navigation in Canada
JointPoint obtained Health Canada licenses for ELITE and PRO surgical navigation systems, allowing for immediate deployment of these products in the region. Jan 03, 2019
Zimmer Biomet Gains FDA Clearance for ROSA Knee System
Zimmer Biomet received FDA 510(k) clearance to market the ROSA® Knee System for robotically-assisted total knee replacement. Jan 02, 2019
