W. L. Gore and Associates, Inc.

3 FDA 510(k) medical device clearances.

Top product codes for W. L. Gore and Associates, Inc.

Recent clearances by W. L. Gore and Associates, Inc.

K222919 — GORE® ENFORM Biomaterial OXF · 2022-12-19
K180919 — GORE Tri-Lumen Catheter DQY · 2018-10-05
K172567 — GORE Molding and Occlusion Balloon Catheter MJN · 2018-01-31

Data sourced from openFDA. This site is unofficial and independent of the FDA.