PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2116468
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2116468
According to Mordor Intelligence, the peripheral vascular devices and accessories market size is expected to grow from USD 18.41 billion in 2025 to USD 19.38 billion in 2026 and is forecast to reach USD 25.07 billion by 2031 at 5.28% CAGR over 2026-2031.

This report Segments the Industry Into by Product Type (Devices and Accessories), by Application (Peripheral Artery Disease, Deep Vein Thrombosis and More), by End User (Hospitals, Ambultory Surgical Centers and More) and Geography (North America, Europe, Asia-Pacific and More). The Market Forecasts are Provided in Terms of Value (USD).
More than 20 million U.S. adults live with PAD, and growth in the 65-plus population is increasing procedure volumes. Elderly patients frequently present multivessel, calcified lesions that require premium drug-coated balloons, bio-absorbable scaffolds and advanced atherectomy tools. Medicare reimbursement for outpatient vascular interventions broadens access, and hospital networks lean on same-day discharge pathways to manage capacity. Demand for patient-specific grafts is rising because anatomical variability increases with age, supporting early adoption of 3-D-printed or tissue-engineered options. Collectively, the demographic wave sustains double-digit growth in the high-value device sub-segments of the peripheral vascular devices and accessories market.
Clinical evidence indicates that endovascular approaches reduce complications and speed recovery compared with open surgery, with ASCs emerging as the fastest-growing site of service and spurring compact, integrated device designs, while drug-coated balloons and intravascular lithotripsy catheters deliver hospital-level outcomes without major capital outlays, and CMS now provides distinct outpatient reimbursement codes for these technologies. As payers lean on bundled payments, suppliers that bundle devices, navigation software and post-procedure monitoring apps gain negotiating leverage.
Since September 2024 European regulators demand deeper clinical datasets and ongoing post-market surveillance before renewing licenses, lengthening development timelines and raising compliance costs . The U.S. Quality System Regulation rewrite, effective February 2026, mirrors ISO 13485 and obliges manufacturers to document risk-management loops from design through end of life. Mid-size firms struggle to bankroll new randomized trials, which accelerates consolidation as they seek the shelter of multinationals' regulatory infrastructures. While the bar deters fast followers, first movers with mature quality systems turn the compliance burden into a durable moat within the peripheral vascular devices and accessories market.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
The device category accounted for 73.85% of peripheral vascular devices and accessories market share in 2025, anchored by percutaneous transluminal angioplasty (PTA) balloons and self-expanding stents with proven long-term patency. Drug-eluting formulations and next-generation nitinol architectures allow these workhorse products to defend unit prices even as hospitals push bulk-buy contracts. Atherectomy and thrombectomy systems deepen margins by addressing calcific, chronic total occlusion and venous thromboembolism cases that demand specialized toolkits. IVC filters and embolic-protection lines remain smaller niches, yet their critical safety roles secure formulary access.
Accessories, although accounting for only 26.15% of 2025 revenue, are projected to outpace the parent class at a 5.94% CAGR through 2031, thereby lifting the overall peripheral vascular devices and accessories market size trajectory. Hydrophilic-coated guidewires, torque-responsive catheters and steerable sheaths shorten procedure times in tortuous anatomy, directly translating into ASC throughput gains. Vascular closure devices such as MYNX CONTROL cut time-to-ambulation by more than 50%, aligning with value-based metrics. Compression systems and pressure-monitoring kits unlock post-discharge revenue streams and embed vendors deeper into episode-of-care economics.
North America delivered 39.92% of global revenue in 2025, powered by early reimbursement for breakthrough devices such as Abbott's Esprit BTK dissolving scaffold and Humacyte's SYMVESS tissue-engineered vessel . The region's hospitals adopt predictive analytics to flag restenosis risk, and payers expand peripheral bundles that reward durable patency. M&A activity-Stryker's USD 4.9 billion Inari purchase and Boston Scientific's serial bolt-ons-reflect scale plays to defend share amid price compression. Canada and Mexico trail U.S. adoption curves by two to three years but accelerate catheter-lab capacity expansion under public-private partnership models.
Europe balances innovation leadership against intensified regulation. Full EU-MDR enforcement forces companies to run longer pivotal trials, stretching average approval timelines past 24 months. National health systems pivot to value-based procurement, pushing suppliers to package devices with training, registries and remote monitoring. Germany and the United Kingdom remain the top adopters of AI-guided imaging, while France channels stimulus funds into outpatient facility upgrades. Southern European nations emphasize cost-effective DES and guidewire kits to manage rising PAD burden without inflating hospital budgets.
Asia-Pacific is the fastest-growing theatre, set to grow at 7.05% CAGR through 2031. China's central government is underwriting cath-lab rollouts in more than 120 tier-2 cities, directly fueling bulk tenders for balloons, stents and IVL consoles. Local manufacturing incentives reduce tariff barriers and encourage Western OEMs to form joint ventures for value-engineering. Japan's super-aged society drives demand for low-contrast, low-radiation tools, and insurers reimburse IVL at hospital-outpatient parity to cut length of stay. India expands private cardiac-care chains, seeking mid-price devices that balance cost and durability, while Australia and South Korea prioritize AI-enabled guidance to offset interventional radiologist shortages. Collectively, the region reshapes competitive dynamics by favoring companies that tailor portfolios to diverse price points within the peripheral vascular devices and accessories market.