Press Release
Posted June 7, 2017
W. L. Gore & Associates, Inc. (Gore) has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its GORE® SYNECOR Preperitoneal Biomaterial hernia repair device.
Press Release
Posted June 6, 2017
Gore has introduced the new GORE® PHASEFLEX® Microwave/RF Test Assemblies, Type 0N for High Density Test/Interconnection – a lightweight assembly that ensures consistent, repeatable measurements with stable electrical performance up to 50 GHz.
Gore will be featuring several new developments at IMS 2017, June 6-8, at the Hawai’i Convention Center, Honolulu, HI, Booth #1740.
Press Release
Posted June 5, 2017
Gore will present its most extensive collection of new and proven products at the largest international air show in Paris, June 19-25, at Hall 2B, Stand F170.