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CARDIOVASCULAR
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Xience Family of Drug-Eluting Stents

The XIENCE™ DES is proven to offer unparalleled patient outcomes during and long after percutaneous coronary interventions (PCI).1 Implanted in over 15 million patients and studied in 120+ clinical trials,* XIENCE™ Stent provides consistent long-term safety data out to 10 years.2 XIENCE™ Stent allows interventional cardiologists (ICs) to achieve the positive outcomes they want for their patients.

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Now CE Marked -
1-month DAPT indication for
High Bleeding Risk Patients

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XIENCE Skypoint™ Drug Eluting Stent System

The newest DES in the XIENCE™ Family, XIENCE Skypoint™ Stent has an enhanced design that offers better expansion, excellent deliverability, a new 48 mm design, and trusted patient outcomes.1,3

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Xience Sierra

XIENCE Sierra™ Drug Eluting Stent System

XIENCE Sierra™ Stent has an enhanced design that offers deliverability, pushability, post dilatation expansion as well as an ultra-low profile and smoother crossing.†

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Xience Sierra

* Data on file at Abbott. The 15 million implants is based on DES data through Q1 2020.

† Tests performed by and data on file at Abbott.

References

  1. Zanchin C, et al. JACC Cardiovasc Interv. 2019;12(17):1665-1675. • Serruys P, et al. N Engl J Med. 2010;363(2):136-146. • Shiomi H, et al.  JACC Cardiovasc Interv. 2019;12:637-647. • Kufner S, et al. Circulation. 2019:139(3):325-333. • Palmerini T, et al. Lancet. 2012;379(9824);1393-1402. • Bangalore S, et al. Circ Cardiovasc Interv. 2013;6:378-390. • Pilgrim T, et al. Lancet. 2014;384:2111-2122. • Pilgrim T, et al. Lancet 2018;392:737-746.
  2. Kufner S, et al. Circulation. 2019:139(3):325-333. Shiomi H, et al. J Am Coll Cardiol Interv. 2019;12:637-647.
  3. XIENCE Skypoint™ Stent Instructions for use. Tests performed and data on file at Abbott - 3.0 x 18 mm stents tested using a simulated arterial model. Data on file at Abbott.

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