New degree of control

Offering the only on-label EVAR solution in highly angulated or short aortic necks, the conformable stent graft and innovative delivery system builds on the proven performance of the GORE® EXCLUDER® Device family.  

Short neck length: down to 10 mm  
High neck angulation: up to 90°  
Small diameter neck: down to 16 mm

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    Adapts to challenging anatomy

    • Nesting stent rows help achieve optimal aortic wall apposition.
    • Individual stent rings adapt closely to the anatomy to maximize the seal. 
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    Improves ease of repositioning

    • Reconstrainable proximal anchors for refined positioning.  
    • Initial trunk deployment at ~70% diameter. 
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    Aids orthogonal placement

    • Optional angulation control at 2 stages.  
    • Helps optimize seal in highly angulated necks. 
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    Active infrarenal fixation

    • Anchors engineered to provide migration resistance.
    • Reduced risk of renal impairment. 

    Proven long-term performance in complex cases

    5-year outcomes from the pivotal trial: The performance of the EXCLUDER® Conformable Device in abdominal aortic aneurysms (AAA) was assessed in an investigational, prospective, multicenter non-randomized pivotal trial that enrolled 80 patients in the Short Neck Substudy from 31 U.S. sites.1

    This is a landmark indication for an EVAR device, equipping physicians with an on-label solution for more patients with hostile neck anatomy.

    Robert Rhee, M.D., Brooklyn, New York, National Principal Investigator

    Healthcare professional examining a patient

    Dedicated clinical device expertise to facilitate complex cases

    • Pre-case planning and procedural consultation.
    • Representatives support hundreds of aortic cases per year, so you’re backed by deep expertise. 

    The next generation in aortic accessories

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    Related to this product

    1. Suckow BD, Oderich GS, Almadani MW, et al. Five-year pivotal trial outcomes of the GORE® EXCLUDER® Conformable Endoprosthesis implanted in abdominal aortic aneurysms with short non-angulated infrarenal seal zones. Journal of Vascular Surgery 2025;793–801.
    IFU Consult instructions

    Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly

    GORE® EXCLUDER® Conformable AAA Endoprosthesis

    INDICATIONS FOR USE IN EUROPE: 
    Trunk-Ipsilateral Leg Endoprosthesis and Contralateral Leg Endoprosthesis Components
    The GORE® EXCLUDER® Conformable AAA Endoprosthesis is intended to exclude the aneurysm from the blood circulation in patients diagnosed with infrarenal abdominal aortic aneurysm (AAA) disease and who have appropriate anatomy as described below:

    • Adequate iliac / femoral access
    • Infrarenal aortic neck treatment diameter range of 16–32 mm
    • A minimum aortic neck length of 10 mm when proximal aortic neck angulation is ≤ 60°
    • A minimum aortic neck length of 15 mm when proximal aortic neck angulation is ≤ 90°
    • Iliac artery treatment diameter range of 8–25 mm and iliac distal vessel seal zone length of at least 10 mm

    Aortic Extender Endoprosthesis and Iliac Extender Endoprosthesis Components
    The Aortic and Iliac Extender Endoprostheses are intended to be used after deployment of the GORE® EXCLUDER® Conformable AAA Endoprosthesis. These extensions are intended to be used when additional length and / or sealing for aneurysmal exclusion is desired. 

    CONTRAINDICATIONS: The GORE® EXCLUDER® Conformable AAA Endoprosthesis is contraindicated in: 

    • Patients with known sensitivities or allergies to the device materials.
    • Patients with a systemic infection who may be at increased risk of endovascular graft infection. 
    Product may not be available in all countries. Please check with your Gore representative for availability.
    25AR2033-EN02 MAT-0663-1