Skip to main content

20 Results for “synecor”

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

Unique Biomaterial for Hernia Repair Receives FDA 510K Clearance

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

Gore Launches Clinical Quality Improvement (CQI) Project of New Hernia Repair Device

New research methodology will procure real world feedback from surgeons and patients to improve outcomes with GORE® SYNECOR Biomaterial

Physicians Report Early Successes Across Multiple Applications in First-in-Human Uses of GORE® SYNECOR Preperitoneal Biomaterial Hernia Repair Device

New three-layer hybrid biomaterial, ideal for TAR procedures, offering permanent strength and rapid tissue generation for single-stage repairs

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.

W. L. Gore & Associates Receives Innovative Technology Designation from Vizient, Inc. for GORE® SYNECOR Biomaterial

Designation recognizes products that bring improvements to the healthcare industry