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  • Trusted Performance

    Today2016

    GORE® EXCLUDER® Iliac Branch Endoprosthesis (IBE) is the
    only iliac branch solution to receive FDA approval

    250,000 clinical implants of GORE® EXCLUDER® Device Trunk-Ipsilateral Legs

    2015

    1,000 clinical implants of IBE

    2014

    Profile is reduced to 16 Fr for 23 and 26 mm Trunk-Ipsilateral Legs and Aortic Extenders

    2013

    Gore® EXCLUDER ® Iliac Branch Endoprosthesis received CE Mark

    2012

    CE Mark and FDA approval received for 35 mm Trunk-Ipsilateral Legs

    Profile of 31 mm Trunk-Ipsilateral Legs and larger Contralateral Legs are reduced

    2011

    23 and 27 mm Contralateral Leg introduced

    2010

    Gore® C3® Delivery System received CE Mark and FDA approval

    2009

    31 mm Trunk-Ipsilateral Legs received FDA approval

    2005

    Six 12 cm Trunk-Ipsilateral Leg configurations added

    2004

    A low permeability GORE® EXCLUDED® Device design introduced

    2003

    31 mm Trunck-Ipsilateral Legs launched in Europe

    Nine additional Contralateral Leg configurations added

    2002

    FDA approved the GORE® EXCLUDER® AAA Endoprosthesis

    1997

    The original GORE® EXCLUDER® AAA Endoprosthesis launched in Europe