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Resources tagged with “clearance”

Gore Receives FDA Clearance for GORE® SYNECOR Preperitoneal Biomaterial Hernia Repair Device

Hybrid of unique bioabsorbable and permanent materials provide a single-stage hernia repair to help minimize complications in preperitoneal applications

Jun 7, 2017

FDA Approves GORE® CARDIOFORM Septal Occluder for PFO Closure to Prevent Recurrent Ischemic Stroke

Gore REDUCE Clinical Study demonstrated 77 percent relative reduction in recurrent ischemic stroke when PFO closure was combined with antiplatelet therapy, compared to antiplatelet therapy alone

Apr 3, 2018

Gore Launches Unique Biomaterial for Complex Ventral Hernia Repair

Gore to launch its new hybrid device, GORE® SYNECOR Biomaterial, at the 17th Annual Hernia Repair Conference in Washington, D.C.

Mar 30, 2016

GORE® DrySeal Flex Introducer Sheath Advances Care through Access

New sheath provides exceptional access to challenging anatomies and branch vessels

Aug 30, 2016

First Successful Implant of GORE® SYNECOR Biomaterial in a Ventral Hernia Patient

Unique biomaterial for hernia repair implanted for the first time in Gore’s Clinical Quality Improvement project

Apr 25, 2016