Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact