FDA 510(k) Applications Submitted by W.L. Gore & Associates, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K173333 10/23/2017 GORE ENFORM Biomaterial W.L. Gore & Associates, Inc.
K170740 03/10/2017 GORE VIABIL Short Wire Biliary Endoprosthesis W.L. Gore & Associates, Inc.
K191773 07/02/2019 GORE BIO-A Tissue Reinforcement W.L. Gore & Associates, Inc.
K051267 05/16/2005 GORE RESOLUT REGENERATIVE MATERIAL, GORE RESOLUT XT REGENERATIVE MEMBRANE, GORE OSSEOQUEST REGENERATIVE MEMBRANE W.L. GORE & ASSOCIATES, INC.
K160254 02/01/2016 GORE DrySeal Flex Introducer Sheath W.L. GORE & ASSOCIATES, INC.


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