Interventional Cardiology Devices Market Trends

Statistics for the 2023 & 2024 Interventional Cardiology Devices market trends, created by Mordor Intelligenceā„¢ Industry Reports. Interventional Cardiology Devices trend report includes a market forecast to 2029 and historical overview. Get a sample of this industry trends analysis as a free report PDF download.

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Market Trends of Interventional Cardiology Devices Industry

Drug-eluting Stents Segment Is Expected to Witness Significant Growth Over The Forecast Period

Drug-eluting stents are coated with a slow-release medication to help prevent blood clots from forming in a stent. This helps the artery remain smooth and open, ensuring good blood flow. These stents are usually used for the lower extremities, and they provide results that are better than self-expanding and balloon-expanding stents. 

Thus, the growing adoption of advanced cardiovascular treatments and the increased funding and technological advancements in the field of cardiology are expected to be the major drivers for the growth of the segment. For instance, according to the study published by the National Institute of Health in February 2022, to reduce in-stent restenosis, coronary drug-eluting stents were developed. Drug combinations having several effects or use for various actions are both delivered through the drug-eluting stent. Thus, the benefits of the drug-eluting stent to a delivered combination of drugs are expected to increase its adoption and are anticipated to boost the segment's growth.

Companies are introducing new and more sophisticated drug-eluting stent systems, which are anticipated to significantly support the growth of the segment. For instance, in August 2021, SINOMED, a medical device company, reported commercial implantation of the HT Supreme Drug-eluting Stent (DES) at the University Hospital Galway, in partnership with the National University of Ireland Galway, marking the start of its European launch.

 Similarly, in May 2022, Medtronic plc received U.S. FDA approval for the Onyx Frontier drug-eluting stent (DES). As the latest evolution in the Resolute DES family, Onyx Frontier DES leverages the same stent platform as Resolute Onyx DES, with an enhanced delivery system. Likewise, in January 2021, Boston Scientific received FDA approval for its Synergy Megatron Drug Eluting stent system, which is designed for the treatment of large coronary arteries near the aorta.

Thus, owing to the aforementioned factors, such as the growing adoption of advanced cardiovascular treatments and the increased funding and technological advancements in the field of cardiology, the drug-eluting stents segment is expected to register healthy growth over the forecast period.

Interventional Cardiology Devices Market: Estimated Number of People Living with Cardiovascular Diseases (In Million), By Region, United Kingdom, 2021

North America is Expected to Show a Significant Growth in Market Over the Forecast Period

North America is expected to hold significant market growth throughout the forecast period. The favorable government initiatives for product development and high patient awareness levels, coupled with an increasing target patient population and an increase in the geriatric population, are expected to be some of the prominent drivers for the growth of the interventional cardiology devices market over the coming years in the region. For instance, according to the World Bank update in 2022, the estimated population of ages 65 and above was 10.5 million in 2021. Thus, with the high burden of target disease and an increase in the geriatric population, the market is expected to increase the demand for interventional cardiology devices, thereby driving the market's growth.

Additionally, a few key market players in the region are developing novel products and technologies to compete with existing products, while others are acquiring and partnering with other companies trending in the market. For instance, in June 2021, Abbott received the United States Food and Drug Administration's approval for its XIENCE family of stents for its one-month dual-antiplatelet therapy (DAPT) labeled for high bleeding risk (HBR) patients in the United States. Similarly, in March 2021, the U.S. FDA approved, one of the first in the world, non-surgical heart valve to treat pediatric and adult patients with a native or surgically repaired right ventricular outflow tract (RVOT), the part of the heart that carries blood out of the right ventricle to the lungs.

Thus, owing to the aforementioned factors such as favorable government initiatives for product development, and high patient awareness levels, coupled with an increasing target patient population and an increase in the geriatric population, the market studied is anticipated to witness steady growth in the North American region over the forecast period.

Interventional Cardiology Devices Market - Growth Rate by Region

Interventional Cardiology Devices Market Size & Share Analysis - Growth Trends & Forecasts (2024 - 2029)