First Patient Enrolled in Gore TAG Thoracic Branch Endoprosthesis LSA Feasibility Study
Multi-Center Study to Assess Feasibility of Gore Device to Treat Historically Challenging Patient Population
Multi-Center Study to Assess Feasibility of Gore Device to Treat Historically Challenging Patient Population
New data from Gore REVISE Clinical Study published online in Journal of Vascular Surgery illustrates role device can play in maintaining and salvaging failing dialysis circuits
108 patient trial to add evidence for treatment of in-stent restenosis using the GORE® VIABAHN® Endoprosthesis
GORE® SYNECOR Biomaterial combines strength of PTFE with the tissue-building scaffold of GORE® BIO-A® Web to create an improved device for hernia repair
Market-leading stent-graft has evolved to address range of indications, patient needs
GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis Provides Improved Outcomes in Real-World Peripheral Arterial Disease Cases
W. L. Gore & Associates (Gore) today announced a favorable ruling involving the GORE® HELEX® Septal Occluder.
Unique biomaterial for hernia repair implanted for the first time in Gore’s Clinical Quality Improvement project
Presentations and Discussions from the Surgical Bypass Summit Available at www.surgicalbypass.com
Study met its primary endpoint with PFO closure in conjunction with antiplatelet therapy, reducing recurrent stroke by > 75% over antiplatelet therapy alone