FIRST PATIENTS ENROLLED IN THE GORE VBX FORWARD CLINICAL STUDY
/PRNewswire/ -- W. L. Gore & Associates, Inc. (Gore) announced today that the first patients have been enrolled in the Gore VBX FORWARD Clinical Study...
Source: prnewswire.com
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THE GORE RELIEF CLINICAL STUDY BEGINS RANDOMIZING PATIENTS TO EVALUATE PFO CLOSURE FOR MIGRAINE HEADACHE RELIEF
/PRNewswire/ -- W. L. Gore & Associates (Gore) announces that patients have passed through the multi-month enhanced screening process and have begun entering...
Source: prnewswire.com
GORE ANNOUNCES FIRST U.S. ENROLLMENT FOR THE GORE® VIAFORT VASCULAR STENT IVC STUDY
/PRNewswire/ -- W. L. Gore & Associates (Gore) has announced that the first U.S. patient has been enrolled in a prospective, non-randomized, multicenter,...
Source: prnewswire.com
GORE INITIATES THE RELIEF CLINICAL STUDY EVALUATING PFO CLOSURE FOR MIGRAINE HEADACHE RELIEF
/PRNewswire/ -- W. L. Gore & Associates (Gore) announced today that it is initiating the RELIEF Clinical Study – an investigational study to evaluate the...
Source: prnewswire.com
W.L. Gore & Associates Launches GORE® SYNECOR Intraperitoneal Biomaterial In Europe, The Middle East And South Africa
(1) and surgeons need a high-quality material for hernia repair in complex patients (VHWG 2). (2) FLAGSTAFF, Ariz., Feb. 22, 2021 /PRNewswire/ -- W. L. Gore & Associates (Gore) announced that GORE SYNECOR Intraperitoneal Biomaterial is now available in Europe, Middle East and South Africa. The device was designed to address unmet needs in complex hernia repair, providing rapid vascularity 3 and permanent strength with a low profile for single, effective hernia repair. GORE® SYNECOR Intraperitoneal Biomaterial offers a tri-layer hybrid solution that supports single, effective hernia repair in...
Source: prnewswire.com