Stents Market Size and Share
Stents Market Analysis by Mordor Intelligence
The stents market is valued at USD 15.05 billion in 2025 and is forecast to reach USD 18.91 billion by 2030, expanding at a 4.67% CAGR. Sustained procedure volumes in coronary artery disease, wider adoption of minimally invasive peripheral interventions and steady product launches are keeping revenue on an upward trajectory. Consolidation among leading manufacturers is improving global reach and distribution efficiency, while health-system migration toward outpatient settings is reshaping procurement dynamics. Policymaker support for early discharge and bundled payments is accelerating purchases of devices that shorten hospital stays, driving hospitals and ambulatory surgical centers to upgrade stent inventories. In parallel, artificial-intelligence tools for vessel sizing and real-time decision support are enhancing implantation accuracy and reducing costly complications, reinforcing long-term demand in the stents market.
Key Report Takeaways
- By product type, coronary stents held 55.12% of stents market share in 2024, whereas peripheral stents are projected to expand at a 7.34% CAGR through 2030.
- By material, metallic biomaterials accounted for 63.24% of the stents market size in 2024; polymeric biomaterials are advancing at an 8.68% CAGR to 2030.
- By end user, hospitals commanded 57.25% share of the stents market size in 2024, while ambulatory surgical centers are growing at an 8.91% CAGR.
- By geography, North America led with 34.45% stents market share in 2024; Asia-Pacific is forecast to grow at an 8.78% CAGR to 2030.
Global Stents Market Trends and Insights
Drivers Impact Analysis
| Driver | (~) % Impact on CAGR Forecast | Geographic Relevance | Impact Timeline |
|---|---|---|---|
| Increasing Prevalence Of Coronary & Peripheral Arterial Disease | +1.2% | Global, with highest impact in APAC and MEA | Long term (≥ 4 years) |
| Rising Burden of Lifestyle-Related Disorders Coupled with Aging Population | +0.9% | Global, most pronounced in developed economies | Long term (≥ 4 years) |
| Rapid Uptake Of Transradial PCI & Day-Case Procedures | +0.8% | North America & Europe, expanding to APAC | Medium term (2-4 years) |
| Technological Shift To Polymer-Free DES & Bioresorbables | +0.6% | Global, led by developed markets | Medium term (2-4 years) |
| Growth in Minimally-Invasive Therapies and Endovascular Procedures | +0.5% | Global, strongest in value-based care markets | Short term (≤ 2 years) |
| AI-Driven Precision Sizing & Deployment Platforms | +0.4% | North America & Europe initially | Long term (≥ 4 years) |
| Source: Mordor Intelligence | |||
Increasing Prevalence of Coronary & Peripheral Arterial Disease
Peripheral arterial disease affects an estimated 200–250 million people worldwide and shows marked variation in regional prevalence, ranging from 5.6% in North America to 14.5% in South-Central Asia.[1]European Journal of Preventive Cardiology, “Global Prevalence of Peripheral Artery Disease,” academic.oup.com Demographic aging and persistent smoking and hypertension rates—contributing 45.6% and 35.1% of peripheral disease risk respectively—are sustaining a large pool of candidates for vascular interventions. As diagnostics improve and awareness rises in emerging economies, demand for both coronary and peripheral stents strengthens, positioning disease prevalence as the prime long-term growth catalyst for the stents market.
Rapid Uptake of Transradial PCI & Day-Case Procedures
Transradial access adoption climbed from 15.9% to 69.1% across recent study periods, reducing bleeding events and enabling same-day discharge protocols. The American Heart Association endorsed transradial approaches for peripheral interventions in 2025, broadening clinical applications. Ambulatory surgical centers billing for PCI increased from 30 sites in 2019 to 65 in 2023, illustrating procedure migration away from inpatient settings.[2]AORN, “Cardiology Codes ASC Leaders Need to Know,” aorn.orgThese patterns are accelerating device demand among outpatient providers and reinforcing value-based care initiatives in the stents market.
Technological Shift to Polymer-Free DES & Bioresorbables
Abbott’s Esprit BTK scaffold became the first FDA-approved dissolving stent for below-the-knee disease in 2024, highlighting momentum behind polymer-free drug-eluting and bioresorbable technologies. Peer-reviewed data show significantly lower inflammation and improved vessel healing versus permanent polymers. Such innovations align with the “leave nothing behind” philosophy, differentiate competitor offerings and are expected to raise the innovation benchmark across the stents market.
AI-Driven Precision Sizing & Deployment Platforms
The FLAVOUR II trial demonstrated that AI-derived fractional flow reserve delivered outcomes on par with intravascular ultrasound while simplifying workflows. HeartFlow’s automated CT analysis provides plaque morphology and optimal sizing guidance, improving operator confidence during stent deployment. Medtronic’s USD 75 million investment in CathWorks signals strategic commitment to AI-enabled diagnostics. These platforms enhance procedural outcomes and standardize decision-making, supporting sustained adoption in the stents market.
Restraints Impact Analysis
| Restraint | (~) % Impact on CAGR Forecast | Geographic Relevance | Impact Timeline |
|---|---|---|---|
| Stringent Multi-Region Approval Timelines | -0.7% | Global, most pronounced in emerging markets | Medium term (2-4 years) |
| High And Rising Product Recall Costs | -0.5% | North America & Europe primarily | Short term (≤ 2 years) |
| Shrinking Reimbursement Gap Vs. Drug-Coated Balloons | -0.4% | Developed markets with established DCB adoption | Medium term (2-4 years) |
| Nickel-Hypersensitivity Litigation Risk | -0.2% | North America & Europe | Long term (≥ 4 years) |
| Source: Mordor Intelligence | |||
Stringent Multi-Region Approval Timelines
Manufacturers must reconcile divergent regulatory pathways as the FDA aligns Quality System Regulation amendments with ISO 13485 while Europe enforces Medical Device Regulation, extending time-to-market. Emerging countries introduce additional clinical evidence requirements, forcing companies to stagger launches and increasing compliance costs. Large incumbents with robust regulatory teams can absorb delays, but smaller innovators face barriers that may slow new entrants into the stents market.
High and Rising Product Recall Costs
Recent Class I recalls—Medtronic’s Pipeline Vantage and Philips’ Tack System—underscore the financial and reputational impact of safety events.[3]U.S. Food and Drug Administration, “Class 1 Device Recall Medtronic Pipeline Vantage Embolization Device,” fda.gov Boston Scientific’s recall of the Obsidio embolic device resulted in multiple injuries and fatalities, elevating scrutiny and insurance premiums. Ongoing post-market surveillance investments redirect R&D budgets and compress margins, tempering innovation momentum across the stents market.
Segment Analysis
By Product: Coronary Dominance Amid Peripheral Acceleration
Coronary stents accounted for 55.12% of stents market share in 2024 on the back of entrenched procedure volumes in multivessel disease. Drug-eluting models featuring ultrathin struts and biodegradable polymers remain the default choice, while bare-metal designs fulfill niche needs that require shorter dual antiplatelet therapy. Peripheral stents, however, are forecast to grow at a 7.34% CAGR, driven by expanding treatment indications for iliac and femoropopliteal lesions and better device trackability in tortuous anatomy. Abbott’s FDA nod for a bioresorbable scaffold below the knee illustrates momentum toward “leave nothing behind” options in peripheral disease.
The stents market size for peripheral interventions is projected to expand steadily as screening programs and duplex ultrasound accessibility improve in emerging economies. Stent grafts for complex aortic aneurysms continue to evolve with branched and fenestrated designs that reduce endoleak risk, while neurovascular flow-diverters capture attention for wide-necked aneurysms. Manufacturers are integrating hydrophilic coatings and AI-enabled deployment feedback to improve outcomes in difficult vascular territories.
Note: Segment shares of all individual segments available upon report purchase
By Material: Metallic Foundation With Polymeric Innovation
Metallic biomaterials remained the backbone of the stents market, claiming 63.24% revenue in 2024 because cobalt-chromium alloys offer high radial strength and corrosion resistance. Stainless steel retains a cost advantage in price-sensitive segments. Nonetheless, polymeric scaffolds are the fastest-advancing category at an 8.68% CAGR, reflecting clinical enthusiasm for biodegradable solutions that minimize chronic inflammation. Magnesium-based constructs exhibit 2.8% platelet adherence versus 5.8% for stainless steel in preclinical models, indicating lower thrombogenicity.
Natural biomaterial coatings such as recombinant humanized collagen foster rapid endothelialization and are likely to carve out specialized niches for drug-free devices. Controlled-release polymer matrices now enable synchronized drug elution with scaffold resorption, addressing previous concerns over mechanical integrity. Economies of scale and manufacturing advances will continue to lower production costs, helping premium polymeric devices penetrate mainstream segments of the stents market.
By Application: CAD Leadership Challenged by Neurovascular Growth
Coronary artery disease accounted for 48.36% of total procedures in 2024 thanks to established reimbursement and long clinical heritage across regions. Neurovascular interventions, however, are pacing fastest at a 7.67% CAGR as expanded time windows and improved recanalization rates boost thrombectomy adoption. Flow-diverting stents and braided constructs tailored for curved intracranial vessels are enabling minimally invasive stroke treatment. Peripheral arterial disease procedures are also climbing, particularly below the knee where restenosis rates historically limited success.
Non-vascular applications, including gastrointestinal strictures and tracheobronchial obstructions, remain niche but highlight the breadth of material science advances. Future growth in endoluminal applications will depend on development of migration-resistant designs and drug-free surface modifications that cut infection risk, expanding the clinical footprint of the stents market.
Note: Segment shares of all individual segments available upon report purchase
By End User: Hospital Consolidation Amid ASC Migration
Hospitals continued to dominate procurement with 57.25% of global revenue in 2024 thanks to emergency readiness, hybrid operating theaters and multidisciplinary teams. Nevertheless, ambulatory surgical centers are projected to grow at an 8.91% CAGR, supported by CMS reimbursement additions that permit same-day PCI and peripheral procedures. Private-equity roll-ups of cardiology practices—342 locations acquired between 2021 and 2023—are centralizing purchasing, creating bargaining power and fostering standardized device portfolios. Cardiac catheterization laboratories in community hospitals still handle complex cases requiring hemodynamic monitoring, ensuring a balanced demand landscape in the stents market.
Geography Analysis
North America’s stents market size stood at USD 5.19 billion in 2025, driven by 500,000 annual PCI procedures, sophisticated catheter laboratories and early adoption of AI-guided sizing tools. Favorable reimbursement and clinical guideline updates that endorse day-case PCI support continuous device refresh cycles. Canada’s universal coverage and hospital capital budgets are more measured, yet procedure volumes benefit from aging demographics and rising diabetes prevalence.
Europe displays steady single-digit revenue growth as MDR compliance ensures high product quality and as national health systems favour cost-effectiveness metrics. Germany, France and the United Kingdom remain top spenders, while Southern and Eastern European countries are upgrading cath-lab fleets through EU infrastructure funds. The stents market share across Western Europe is tempered by price controls, but value-based procurement is beginning to reward technologies that shorten dual antiplatelet therapy and reduce rehospitalization.
Asia-Pacific is the largest incremental contributor to future unit demand, with China alone performing over 1 million coronary interventions in 2024. Reforms streamlining local approval for innovative devices are shortening launch timelines, although province-specific catalog pricing creates margin pressures. India’s national insurance scheme broadens access to PCI, while Japan maintains premium pricing for polymer-free and ultra-thin stents due to rapid ageing. Southeast Asian nations are scaling cardiac centers, and public-private partnerships in Indonesia and Vietnam are accelerating infrastructure deployment. Collectively, these trends anchor Asia-Pacific as the fastest-growing region within the stents market.
Competitive Landscape
The stents industry is moderately consolidated. The companies are leveraging broad coronary and peripheral portfolios and aggressive emerging-market expansion. Boston Scientific agreed to acquire Silk Road Medical for USD 1.26 billion to deepen its neurovascular franchise, while Teleflex announced a €760 million purchase of Biotronik’s vascular intervention arm to add specialty devices in lower-limb disease. Abbott’s investments in bioresorbable scaffolds and imaging integration sustain competitive differentiation.
Technology innovation is intense. Companies are pairing hydrophilic coatings with polymer-free drug reservoirs, and investing in AI-driven workflow tools that shorten procedure time. Drug-coated balloons remain a notable substitute threat for small-vessel disease and in-stent restenosis, prompting stent makers to prove superiority through head-to-head trials. Private-equity ownership of large cardiology practices is consolidating buyer power, nudging vendors toward multi-year value-based contracts. Cost-conscious health systems in Europe and parts of Asia are also encouraging price competition, although intellectual property around surface chemistry and scaffold geometry provides some insulation. Mid-size challengers are targeting white-space niches such as pediatric implants and fully degradable peripheral devices, elevating long-term innovation pressure in the stents market.
Stents Industry Leaders
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Boston Scientific Corporation
-
Medtronic PLC
-
Abbott Laboratories
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Becton Dickinson and Company
-
Terumo
- *Disclaimer: Major Players sorted in no particular order
Recent Industry Developments
- June 2025: InspireMD received CE Mark approval under MDR for the CGuard Prime EPS carotid stent system
- May 2025: Terumo Interventional Systems announced early commercial availability of its FDA-approved Roadsaver carotid stent system
- March 2025: Terumo Europe secured MDR approval for expanded indications of Ultimaster Nagomi and Ultimaster Tansei sirolimus-eluting coronary stents
- January 2025: Terumo Europe secured MDR approval for expanded indications of Ultimaster Nagomi and Ultimaster Tansei sirolimus-eluting coronary stents
Research Methodology Framework and Report Scope
Market Definitions and Key Coverage
Our study treats the global stents market as the combined annual sales value of implantable mesh-like tubes designed to keep natural blood vessels or hollow organs open, embracing vascular devices (coronary, peripheral, neurovascular) alongside non-vascular formats such as gastrointestinal, airway, and urological stents. We consider only new, finished devices sold to healthcare providers or distributors and value them in USD at manufacturer selling price.
Scope exclusions include custom stent graft systems fabricated case-by-case for aortic aneurysm repair, dental and orthopedic placeholder implants, and refurbished or re-processed stents, which are excluded from the sizing.
Segmentation Overview
- By Product
- Coronary Stents
- Drug-eluting Stents
- Bare-metal Stents
- Bioabsorbable Stents
- Peripheral Stents
- Iliac Stents
- Femoral-Popliteal Stents
- Renal & Related Stents
- Carotid Stents
- Stent Grafts & Implants
- Coronary Stents
- By Material
- Metallic Biomaterials
- Polymeric Biomaterials
- Natural Biomaterials
- By Application
- Coronary Artery Disease
- Peripheral Artery Disease
- Aortic Aneurysm
- Neurovascular Disease
- Gastrointestinal Obstruction
- Urological Obstruction
- Respiratory Airway Obstruction
- By End User
- Hospitals
- Ambulatory Surgical Centers
- Cardiac Catheterization Labs
- Specialty Clinics
- By Geography
- North America
- United States
- Canada
- Mexico
- Europe
- Germany
- United Kingdom
- France
- Italy
- Spain
- Rest of Europe
- Asia-Pacific
- China
- Japan
- India
- Australia
- South Korea
- Rest of Asia-Pacific
- Middle East and Africa
- GCC
- South Africa
- Rest of Middle East and Africa
- South America
- Brazil
- Argentina
- Rest of South America
- North America
Detailed Research Methodology and Data Validation
Primary Research
Mordor analysts interviewed interventional cardiologists, peripheral vascular surgeons, gastroenterologists, supply-chain managers, and regional distributors across North America, Europe, Asia-Pacific, and Latin America. These discussions clarified the current procedure mix, typical device mark-ups, the pace of bioresorbable adoption, and likely price-volume shifts, letting us adjust desk findings and validate growth drivers.
Desk Research
We began with published procedure statistics and trade data from sources such as the World Health Organization, OECD Health Stats, and Eurostat to pin down national interventional volumes and device import trends. Regulatory filings available through the US FDA 510(k) database, the EU's EUDAMED notices, and Japan's PMDA approvals helped us map product availability timelines and average selling prices. Additional context came from peer-reviewed journals (JACC, Lancet), leading cardiology associations, and hospital procurement portals. Paid datasets like D&B Hoovers and Dow Jones Factiva supplied company revenue splits and recent tender information. The sources cited here are illustrative; many more were reviewed to cross-verify figures and assumptions.
Market-Sizing & Forecasting
A top-down model starts with country-level angioplasty, neurovascular, and endoscopy procedure counts, which are then multiplied by stent utilization rates and blended ASPs. Results are pressure-tested through selective bottom-up checks such as sampled supplier revenues and hospital purchase audits. Key variables include PCI per million population, peripheral artery disease prevalence, elective endoscopy growth, average dual-therapy stent premiums, reimbursement revisions, and currency movements. Forecasts rely on multivariate regression that links stent uptake to disease incidence trends, aging index, and health-expenditure growth, with scenario analysis applied where device price caps or novel scaffold launches may swing demand.
Data Validation & Update Cycle
Outputs pass three analyst reviews, anomaly screens against parallel device categories, and variance checks versus prior editions. Models refresh each year; interim updates are triggered when major regulatory approvals, safety alerts, or reimbursement changes occur. Before release, a fresh validation call with at least one regional Key Opinion Leader ensures the narrative reflects the latest clinical reality.
Why Mordor's Stents Baseline Deserves Confidence
Published figures often diverge because firms pick different device mixes, pricing tiers, and refresh cadences. Our disciplined scope choice and annual reconfirmation of core variables curb that drift.
Key gap drivers include whether non-vascular stents are counted, how ASP erosion is projected, and the year chosen as the base. Some publishers lean on single-region shipment audits or roll forward older ASPs, while Mordor blends procedure data from 40+ countries with live price checks, yielding a balanced, ready-for-boardroom baseline.
Benchmark comparison
| Market Size | Anonymized source | Primary gap driver |
|---|---|---|
| USD 15.05 B (2025) | Mordor Intelligence | - |
| USD 15.38 B (2025) | Regional Consultancy A | Uses inflation-indexed list prices, limited APAC country coverage |
| USD 11.40 B (2024) | Global Consultancy B | Excludes non-vascular stents and applies earlier base year |
| USD 12.61 B (2025) | Industry Association C | Focuses only on cardiovascular stents segment |
In short, by tying market value to verified procedure counts, contemporaneous ASPs, and clearly stated inclusions, Mordor Intelligence delivers a dependable starting point for strategic planning, free from hidden scope shifts or aging assumptions.
Key Questions Answered in the Report
1. What is the current value of the stents market?
The stents market is valued at USD 15.05 billion in 2025 and is projected to reach USD 18.91 billion by 2030.
2. Which product segment generates the highest revenue?
Coronary stents maintain leadership, holding 55.12% of global revenue in 2024.
3. What material is growing fastest in stent manufacturing?
Polymeric biomaterials, particularly bioresorbable scaffolds, are advancing at an 8.68% CAGR through 2030.
4. Why are ambulatory surgical centers important to future growth?
Ambulatory surgical centers enable same-day PCI and peripheral procedures, growing at an 8.91% CAGR as reimbursement expands.
5. Which region shows the strongest growth outlook?
Asia-Pacific is forecast to advance at an 8.78% CAGR, driven by healthcare modernization in China, India and Southeast Asia.
6. How is artificial intelligence influencing stent procedures?
AI tools provide automated vessel sizing, fractional flow reserve assessment and deployment guidance, helping clinicians improve accuracy and reduce complications.
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