In this 15th edition of The RESILIA Tissue Insider, we open 2026 by highlighting key clinical milestones shaping the year ahead for the RESILIA tissue portfolio. This issue explores early European experience with the KONECT RESILIA aortic valved conduit, shares important clinical trial updates, and looks ahead to a major long term durability milestone for RESILIA tissue technology.
As we begin 2026, this edition reflects the continued momentum of the RESILIA tissue portfolio across innovation, clinical experience, and long term evidence generation. From growing European adoption of the KONECT RESILIA aortic valved conduit and early insights into minimally invasive use, to new clinical trial readouts for MITRIS RESILIA valves, this issue underscores the breadth and depth of ongoing clinical engagement. We also look ahead to a pivotal milestone with the upcoming 10 year COMMENCE trial data, while revisiting the 8 year outcomes to provide important context as the evidence base for RESILIA tissue technology continues to mature.
Discover more on RESILIA tissue through the current and past issues below.
In this issue of The RESILIA Tissue Insider, we take you through the past, present and future of the INSPIRIS RESILIA valve in our feature article, before highlighting the most exciting presentations, live cases and symposia talks from the 39th EACTS Annual Meeting in Copenhagen:
This healthcare professional focused booklet explores the latest clinical studies and publications involving the INSPIRIS RESILIA valve and RESILIA tissue through the review of 24 publications and abstracts.
Each reference has been summarized visually over 1 or 2 slides, for you to save time.
*Clinical data on valves with RESILIA tissue up to 7-year follow-up have been published, with additional follow-up to 10-years in progress.
Beaver T, Bavaria JE, Griffith B et al. Seven-year outcomes following aortic valve replacement with a novel tissue bioprosthesis. J Thorac Cardiovasc Surg. 2024; 168: 781–91.
†RESILIA tissue tested against tissue from commercially-available bovine pericardial valves from Edwards in a juvenile sheep model. Flameng, et al. J Thorac Cardiovasc Surg 2015;149:340–5
Refer to device instructions for use for important warnings related to VFit technology. These features have not been observed in clinical studies to establish the safety and effectiveness of the model 11500A for use in valve-in-valve procedures. VFit technology is available on sizes 19–25 mm.
Medical device for professional use. For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the Instructions for Use (consult eifu.edwards.com where applicable).
An educational website focused on TAVI is underway
Thank you. We will keep you updated when new content is available.