PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2113596
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2113596
According to Mordor Intelligence, the artificial blood vessels market size was valued at USD 3.25 billion in 2025 and is estimated to grow from USD 3.45 billion in 2026 to reach USD 4.68 billion by 2031, at a CAGR of 6.25% during the forecast period (2026-2031).

This report is Segmented by Application (Aortic Disease, Peripheral Artery Disease, Hemodialysis, and More), Polymer Type (Polydioxanone, Polyurethane, and More), End User (Hospitals, Ambulatory Surgical Centers, and More), Device Type (Synthetic Vascular Grafts, and More), and Geography (North America, and More). The Market Provides the Value (in USD) for the Above-Mentioned Segments.
Peripheral artery disease affected 113 million people worldwide in 2025, including 6.5 million U.S. patients, and prevalence doubles with each decade of life after age 50. The aging demographic profiles of Japan, Germany, and South Korea therefore anchor long-term demand for durable vascular conduits. While supervised exercise therapy now precedes many interventions per the 2024 guideline, patients who progress to revascularization often present with advanced disease that mandates a reliable graft when autogenous vein is unavailable. Consequently, the Artificial Blood Vessels market benefits from a smaller yet higher-acuity treatment pool.
SYMVESS achieved 67% primary patency at 30 days and became the first tissue-engineered graft cleared in the United States in December 2024. The milestone validated two decades of extracellular-matrix research and is compressing review cycles for follow-on platforms. Bacterial nanocellulose synthesized by Komagataeibacter xylinus replicates collagen's nanofibrillar structure, surpasses 200 MPa tensile strength, and promotes endothelial adhesion, positioning it as the fastest-growing polymer in the Artificial Blood Vessels market. China's TEDA Bioprinting recorded 95% cell viability in 10 cm patient-specific grafts in 2024 and begins clinical trials in 2025.
Medicare's 2025 ambulatory payment range of USD 5,702-17,957 per vascular code does not fully offset total episode-of-care costs, which include premium graft pricing, radiology, anesthesia, and surveillance. BEST-CLI showed 32% fewer major limb events with autogenous vein, reinforcing payer skepticism toward synthetic grafts in infra-inguinal disease. Outside high-income markets, out-of-pocket expenditure above 40% in India and Indonesia narrows the addressable base for bioengineered products.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Traumatic vascular injury drove an 11.25% CAGR outlook from 2026 to 2031, fueled by military procurement and level-1 trauma centers prioritizing shelf-stable grafts that bypass vein harvesting delays. SYMVESS's 67% primary patency and 9% amputation rate in extremity trauma demonstrate outcome parity with legacy synthetics while cutting operative time. Aortic disease, by contrast, retained 42.56% of the Artificial Blood Vessels market share in 2025 behind the ascendancy of thoracic endovascular repair, which now handles 81% of abdominal aneurysm cases in the United States. Open surgical volumes are falling, yet each hybrid stent-graft incorporates polyethylene terephthalate or polytetrafluoroethylene fabric, sustaining material demand. Peripheral artery disease applications encounter guideline-driven headwinds favoring autogenous vein, whereas dialysis vascular access remains resilient due to fistula maturation failure rates that exceed 38%.
Bacterial nanocellulose is on track for a 12.85% CAGR through 2031, propelled by mechanical compliance mirroring collagen and superior cell adhesion that reduces intimal hyperplasia risk. Polyethylene terephthalate kept a 36.53% foothold in 2025 as woven and knitted PET grafts remain the standard for large-diameter aortic repairs, especially in Europe where surgeons value burst strength and kink resistance. Expanded polytetrafluoroethylene continues to dominate small- and medium-diameter bypasses, augmented by heparin-bonded surfaces like PROPATEN that lengthen patency. Hybrid composite polymers are emerging in complex arch repairs, combining polytetrafluoroethylene luminal surfaces with PET structural meshes to balance compliance and radial strength.
North America retained 42.13% of global revenues in 2025 amid substantial Medicare reimbursement, yet vein-first clinical guidance and the competitively successful BEST-CLI study curb infra-inguinal prosthetic usage. Still, 6.5 million U.S. peripheral artery disease patients and a surge in thoracic endovascular repairs sustain baseline demand. Canadian and Mexican uptake trails, but Humacyte's SYMVESS approval sets a precedent that is catalyzing U.S. investigational device submissions for follow-on tissue-engineered grafts.
Asia-Pacific is projected to post the fastest 10.51% CAGR, leveraging high cardiovascular disease prevalence in China and India. However, healthcare spending patterns marked by > 40% out-of-pocket outlays in several markets dampen uptake of premium bioengineered products. China's TEDA Bioprinting is positioning to export patient-specific conduits, while Japan and South Korea apply fast-track approvals for locally manufactured grafts to meet dialysis and peripheral artery disease demand. Australia's universal insurance and South Korea's single-payer system support rapid adoption of endovascular techniques and associated grafts.
Europe's growth lags North America and Asia-Pacific but benefits from a mature vascular surgery infrastructure. The 2025 European Society of Vascular Surgery consensus reported 7.3% in-hospital mortality and 5.0% stroke during arch TEVAR, prompting iterative design upgrades in stent-graft geometry and delivery systems. Germany, France, and the United Kingdom remain volume anchors; Spain and Italy contribute smaller but steady demand. MDR compliance presents cost and time-to-market challenges that favor incumbents, yet CE-first strategies, as executed by PECA Labs with its growth-accommodating exGraft, remain attractive for U.S. start-ups. Latin America and the Middle East & Africa are nascent, with Dubai and Riyadh tertiary centers importing high-end grafts, while Brazil favors cost-effective synthetics in its public system.