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The INSPIRIS RESILIA aortic valve

Inspiris resilia valve

Patients affected by aortic valve disease seek a long-lasting solution that does not limit their future treatment options or impacts their day-to-day life.1

Valve selection is a lifelong commitment which requires careful consideration of valve durability and the impact it could have on possible secondary interventions.

Recommending the right valve means getting closer to valve therapy and therefore to your patients' needs.

The INSPIRIS RESILIA aortic valve offers your patients a solution that's right for today and ready for tomorrow.

Who could benefit today and tomorrow from the INSPIRIS RESILIA aortic valve?

The INSPIRIS RESILIA aortic valve is suitable for a broad range of patients2 while facilitating the lifetime management of their aortic valve disease.

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Phil, 55 years old

  • Manages his own IT business
  • Travels regularly because of work
  • Loves cycling, wherever he might be in the world, as well as sailing
  • Diagnosed with severe aortic stenosis (AS) after a period of increasing difficulty keeping up with his usual physical activity
  • Eligible for surgical aortic valve replacement (SAVR)
  • Keen to get back to doing the things he loves

Anna, 33 years old

  • Primary school teacher
  • Diagnosed with bicuspid aortic valve in her late 20s
  • Graded as having severe AS at her last follow-up appointment
  • Eligible for SAVR
  • Recently married and looking to start a family as soon as possible

Maya, 62 years old

  • Spends most of her time looking after her grandchildren
  • Diagnosed with type 2 diabetes (T2D) in her early 50s
  • Current body mass index (BMI) is 32
  • Despite her best efforts she has been unable to lose weight 
  • Diagnosed with symptomatic severe AS, following a cardiology referral from her endocrinologist
  • Eligible for SAVR
  • Small aortic annulus 

Mo, 66 years old

  • Retired security officer
  • Ex-smoker 
  • As his AS progressed, he had to give up on the weekly game of five a side football with his friends 
  • Eligible for SAVR

The 2021 ESC/EACTS guidelines do not recommend bioprostheses in patients below 60 years of age, however, informed patient preference and lifestyle also plays a critical role in the decision-making process for the choice of prosthetic valve.3

The INSPIRIS RESILIA aortic valve is the market-leading replacement aortic valve

To date, more than 300,000 INSPIRIS RESILIA aortic valves have been implanted into patients worldwide

Help your patients meet the future confidently, with enhanced anti-calcification tissue and VFit technology designed to allow potential future subsequent valve intervention.2, 4–8

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.

Building on a trusted foundation

The INSPIRIS RESILIA aortic valve is the latest generation of aortic tissue valve developed by Edwards Lifesciences, and builds upon the proven Carpentier-Edwards PERIMOUNT Magna Ease aortic valve with additional features.

Building on a trusted foundation table image

*2800TFX model is no longer CE marked and not available for sale.
No clinical data are available that evaluate the long-term impact of the Carpentier–Edwards ThermaFix treatment in patients.
†No clinical data are available that evaluate the long-term impact of RESILIA tissue in patients. The INSPIRIS RESILIA valve alloy band represents 19-25 mm sizes. The sizes 27 and 29 mm do not have VFit technology.

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The INSPIRIS RESILIA aortic valve can be implanted via minimally invasive procedures14 for faster recovery times.15
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Right for today, ready for tomorrow. 

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Abbreviations

AS, aortic stenosis; BMI, body-mass index; SAVR, surgical aortic valve replacement; T2D, type 2 diabetes.

References

  1. Lauck SB et al. Can J Cardiol. 2021;37:1054–63.
  2. Edwards Lifesciences. INSPIRIS RESILIA Aortic Valve, Model 11500A, Instructions for use. 
  3. Vahanian A, et al. Eur Heart J. 2022;43:561–632.
  4. Kottmaier M, et al. Thorac Cardiovasc Surg. 2017;65(3):198–205.
  5. Ruel M, et al. Eur J Cardiothorac Surg. 2005;27(3):425–33.
  6. Beaver T, et al. J Thorac Cardiovasc Surg. 2023;S0022–5223(23)00873–5. 
  7. Flameng W, et al. J Thorac Cardiovasc Surg. 2015;149:340–5.
  8. Edwards LifeSciences. Capping bioprosthetic tissue to reduce calcification. EP3453409A1, European Patent Office (2013). Available at: https://data.epo.org/publication-server/document?iDocId=5871989&iFormat=0. Accessed May 2024.
  9. Edwards Lifesciences. Carpentier-Edwards PERIMOUNT Magna Ease Pericardial Bioprosthesis, Model 3300TFX, Instructions for use. 
  10. Edwards Lifesciences. Carpentier-Edwards PERIMOUNT RSR Pericardial Aortic Bioprostheses, Model 2800 and Model 2800TFX, Instructions for use. 
  11. Ruzicka DJ, et al. Circulation. 2009;120(11 Suppl):S139-45.
  12. De la Fuente AB, et al. J Heart Valve Dis. 2015;24(1):101-9.
  13. Todd TJ, et al. J Mater Sci Mater Med. 2016;27(1):8.
  14. Ahmad AE, et al. Adv Ther. 2021;38(5):2435–46.
  15. Glauber M, et al. J Thorac Cardiovasc Surg. 2013;145(5):1222–6.

No clinical data are available that evaluate the long-term impact of RESILIA tissue in patients. Additional clinical data for up to 10 years of follow-up are being collected to monitor the long-term safety and performance of RESILIA tissue. 


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

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).