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시장보고서
상품코드
2087601
스텐트 그래프트 시장 : 제품 유형별, 적응증별, 전달 메커니즘별, 소재별, 구성별, 최종 사용자별 시장 예측(2026-2032년)Stent Grafts Market by Product Type, Indication, Delivery Mechanism, Material, Configuration, End User - Global Forecast 2026-2032 |
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360iResearch
스텐트 그래프트 시장은 2032년까지 연평균 복합 성장률(CAGR) 8.49%로 성장이 전망되며, 17억 4만 달러 규모로 확대될 것으로 예측됩니다.
| 주요 시장 통계 | |
|---|---|
| 기준 연도 : 2025년 | 9억 6,076만 달러 |
| 추정 연도 : 2026년 | 10억 4,012만 달러 |
| 예측 연도 : 2032년 | 17억 4만 달러 |
| CAGR(%) | 8.49% |
스텐트 그래프트 시장은 복부 대동맥류, 흉부 대동맥류, 대동맥 박리, 외상성 대동맥 손상 및 특정 말초 혈관 질환에 대한 저침습 혈관 복원술로의 전 세계적 전환을 배경으로 형성되고 있습니다. 혈관 내 동맥류 수복술 및 흉부 혈관 내 대동맥 수복술은 해부학적 조건이 적합한 경우, 외과적 침습을 줄이고 입원 기간을 단축하며 고령 환자나 고위험 환자의 치료 적용 범위를 확대할 수 있어 주요 치료법으로 자리 잡고 있습니다.
특히 환자 수가 많은 혈관 센터에서는 기존의 개복 수술에서 영상 유도 하의 혈관 내 치료로 전환이 진행되면서 경쟁 구도가 재편되고 있습니다. 의사들은 해부학적 적합성을 향상시키고, 그래프트의 이동을 줄이며, 복잡한 대동맥 분지의 보존을 지원하고, 굴곡된 혈관 내에서의 전개를 단순화하는 기기를 우선적으로 채택하고 있습니다.
인공지능(AI)은 영상 진단, 해부학적 측정, 시술 계획, 기기 크기 선정 및 경과 관찰을 개선함으로써 스텐트 그래프트의 밸류체인에 누적 영향을 미치고 있습니다. AI를 활용한 CT 혈관조영술의 분할 분석은 임상의가 목 길이, 각도, 혈전량, 장골동맥을 통한 접근, 그리고 동맥류의 형태를 보다 일관되게 정량화할 수 있도록 지원하여, 수술 전 계획의 정확도를 높이고 워크플로우의 편차를 줄이는 데 기여합니다.
아시아태평양은 일본, 중국, 호주, 인도, 한국이 혈관 내 치료 역량을 확대하고 첨단 영상 진단 기술에 투자하고 있어, 스텐트 그래프트 시장에서 가장 활기찬 지역 중 하나가 되었습니다. 일본은 고령화 사회와 확립된 혈관 의료의 혜택을 누리고 있는 반면, 중국과 인도는 진단율 향상, 3차 의료 기관의 확대, CT 혈관조영술에 대한 접근성 확대에 따라 대규모 환자층을 보유하고 있습니다. 호주와 한국에서는 전문 의료 센터에서 첨단 혈관 내 동맥류 치료술이 널리 도입되고 있지만, 신흥 시장 전체의 보급률에는 보험 환급 제도의 편차와 전문의 확보 상황이 계속해서 영향을 미치고 있습니다.
아세안(ASEAN) 국가들의 스텐트 그래프트 접근 환경은 제각각입니다. 싱가포르, 태국, 말레이시아에서는 전문의 체계가 잘 갖춰져 있는 반면, 인도네시아, 베트남, 필리핀에서는 영상 진단 인프라 및 혈관 치료 프로그램의 확충에 따라 점차 확대되고 있습니다. 조달 결정 시에는 대부분의 경우 임상 성능과 합리적인 가격, 사후 서비스, 재고 확보, 의사 교육 간의 균형이 고려됩니다.
미국은 시술 건수, FDA 규제 하의 혁신, 전문의 네트워크, 임상시험 인프라, 그리고 보험 급여의 충실도 덕분에 스텐트 그래프트 시장에서 가장 영향력 있는 시장으로 자리매김하고 있습니다. 한편, 캐나다에서는 각 주의 의료 제도 전반에 걸쳐 근거 기반의 도입이 중시되고 있습니다. 멕시코와 브라질은 민간 병원 수요와 혈관 내 치료 전문 지식의 향상에 힘입어 라틴아메리카에서 중요한 성장 시장이지만, 공공 의료와 민간 의료 환경에 따라 접근성은 상이합니다.
업계 리더는 복잡한 경부 해부학적 구조, 장골동맥 접근의 어려움, 분지 보존, 밀폐 신뢰성 및 장기적인 내구성에 대응할 수 있는 임상적으로 차별화된 기기를 우선적으로 고려해야 합니다. 개창형, 분지형, 저프로파일형 및 컨포머블 스텐트 그래프트 시스템에 대한 투자는 엄격한 근거 창출, 실세계 데이터, 그리고 투명한 시판 후 조사와 병행하여 이루어져야 합니다.
본 조사에서는 1차 정보와 2차 정보를 결합하여 시장의 방향성, 기술 채택 현황, 규제 동향, 임상 실무 패턴 및 지역별 수요 요인을 평가했습니다. 2차 정보에는 공중보건 데이터 세트, 규제 데이터베이스, 임상 지침, 의료기기 승인 기록, 병원 조달 동향, 동료 심사를 거친 문헌, 기업 제출 서류 및 입수 가능한 경우 혈관외과 레지스트리 정보가 포함됩니다.
의료 시스템에서 저침습적 혈관 복원, 조기 진단 및 치료 성과에 기반한 의료기기 선정이 계속해서 중시되는 가운데, 스텐트 그래프트 시장은 앞으로도 지속적인 중요성을 유지할 전망입니다. 고령화, 영상 진단 인프라, 전문의의 전문 지식, 임상적 근거 및 보험 급여 지원이 잘 갖춰진 지역에서 수요가 가장 크게 증가할 것으로 예측됩니다.
The Stent Grafts Market is projected to grow by USD 1,700.04 million at a CAGR of 8.49% by 2032.
| KEY MARKET STATISTICS | |
|---|---|
| Base Year [2025] | USD 960.76 million |
| Estimated Year [2026] | USD 1,040.12 million |
| Forecast Year [2032] | USD 1,700.04 million |
| CAGR (%) | 8.49% |
The stent grafts market is anchored by the global shift toward minimally invasive vascular repair for abdominal aortic aneurysm, thoracic aortic aneurysm, aortic dissection, traumatic aortic injury, and selected peripheral vascular conditions. Endovascular aneurysm repair and thoracic endovascular aortic repair have become central treatment pathways because they can reduce surgical trauma, shorten hospital stays, and expand treatment eligibility for older or higher-risk patients when anatomy is suitable.
Demand is supported by population aging, higher use of CT angiography, improved screening in high-risk groups, and steady innovation in low-profile delivery systems, fenestrated and branched stent grafts, conformable graft materials, and enhanced sealing technologies. The market remains clinically rigorous because product selection depends on anatomy, durability, endoleak risk, access-vessel quality, operator experience, and post-procedure surveillance.
The competitive landscape is being reshaped by the migration from conventional open surgery to image-guided endovascular treatment, particularly in high-volume vascular centers. Physicians are prioritizing devices that improve anatomical fit, reduce graft migration, support complex aortic branch preservation, and simplify deployment in tortuous vessels.
Regulatory and reimbursement pressure is also transforming commercialization. Evidence expectations are rising under frameworks such as the U.S. FDA pathway and the European Medical Device Regulation, while hospitals are assessing total episode cost, reintervention rates, inventory efficiency, and long-term durability. As a result, manufacturers with strong clinical data, physician training programs, quality systems, and reliable supply chains are better positioned than firms competing mainly on price.
Artificial intelligence is cumulatively influencing the stent graft value chain by improving imaging interpretation, anatomical measurement, case planning, device sizing, and follow-up surveillance. AI-enabled segmentation of CT angiography can help clinicians quantify neck length, angulation, thrombus burden, iliac access, and aneurysm morphology more consistently, supporting better preoperative planning and reducing workflow variation.
AI is also becoming relevant after implantation. Algorithms can support detection of sac expansion, endoleak suspicion, graft migration, and surveillance adherence patterns when integrated with imaging systems and electronic health records. Adoption will depend on validated performance, explainability, cybersecurity, interoperability with hospital workflows, and clinician oversight, as AI remains a decision-support tool rather than a substitute for vascular expertise.
Asia-Pacific is one of the most dynamic regions for stent grafts as Japan, China, Australia, India, and South Korea expand endovascular capabilities and invest in advanced imaging. Japan benefits from an older population and established vascular care, while China and India offer large patient pools with increasing diagnosis rates, expanding tertiary hospitals, and broader access to CT angiography. Australia and South Korea show strong adoption of advanced endovascular aneurysm repair in specialist centers, although reimbursement variability and specialist availability continue to influence uptake across emerging markets.
North America remains a leading region due to high procedural maturity, extensive imaging access, strong clinical trial activity, and broad use of EVAR and TEVAR in the United States and Canada. Europe maintains deep clinical expertise across Germany, France, Italy, Spain, and the United Kingdom, although MDR compliance has increased evidence, documentation, and post-market surveillance requirements. Latin America is led by Brazil and Mexico, where private hospitals adopt advanced stent graft devices faster than many public systems. The Middle East, especially GCC markets, is supported by specialty hospitals, cardiovascular investment, and medical tourism, while Africa faces slower adoption due to infrastructure limitations, affordability barriers, uneven imaging access, and trained workforce constraints.
ASEAN presents a mixed access environment for stent grafts, with Singapore, Thailand, and Malaysia showing stronger specialist capacity and Indonesia, Vietnam, and the Philippines expanding gradually as imaging infrastructure and vascular programs scale. Procurement decisions often balance clinical performance with affordability, after-sales support, inventory availability, and physician training.
The GCC benefits from high healthcare spending, tertiary hospital investment, and demand for advanced cardiovascular care, making it attractive for premium stent graft systems. The European Union remains evidence-driven and quality-focused under MDR, favoring suppliers with robust technical documentation, post-market surveillance, and registry-supported outcomes. BRICS countries combine large clinical demand with localization priorities, price sensitivity, and expanding public hospital capacity, while G7 markets shape global standards through clinical evidence, reimbursement scrutiny, technology assessment, and innovation adoption. NATO countries are increasingly attentive to resilient medical supply chains, emergency preparedness, cybersecurity, and continuity of critical vascular device access.
The United States is the most influential stent graft market due to procedure volume, FDA-regulated innovation, specialist networks, clinical trial infrastructure, and reimbursement depth, while Canada emphasizes evidence-based adoption across provincial health systems. Mexico and Brazil are important Latin American growth markets, supported by private hospital demand and improving endovascular expertise, although access differs across public and private care settings.
In Europe, the United Kingdom, Germany, France, Italy, and Spain remain major adopters of abdominal and thoracic stent grafts, with Germany benefiting from high hospital capacity and France and the UK emphasizing structured evaluation, clinical guidelines, and reimbursement discipline. Russia maintains demand for aortic repair but faces procurement, sanctions-related, and supply continuity complexities. China is scaling rapidly through hospital modernization, physician training, and domestic device development, while India is expanding from major metropolitan centers as diagnostic access improves. Japan remains advanced and aging-driven, Australia has strong specialist adoption supported by organized vascular care, and South Korea combines high technology readiness with sophisticated cardiovascular and imaging infrastructure.
Industry leaders should prioritize clinically differentiated devices that address hostile neck anatomy, iliac access challenges, branch preservation, sealing reliability, and long-term durability. Investment in fenestrated, branched, lower-profile, and conformable stent graft systems should be paired with rigorous evidence generation, real-world data, and transparent post-market surveillance.
Commercial success will depend on physician education, case-planning support, local reimbursement strategy, regulatory readiness, and supply reliability. Manufacturers should build AI-ready digital planning ecosystems, partner with imaging and hospital IT providers, and create region-specific portfolios that balance premium innovation with cost-sensitive access. Leaders should also strengthen recall readiness, quality systems, cybersecurity controls, and regulatory documentation to meet expanding global scrutiny.
The research approach combines primary and secondary intelligence to evaluate market direction, technology adoption, regulatory dynamics, clinical practice patterns, and regional demand drivers. Secondary inputs include public health datasets, regulatory databases, clinical guidelines, device approval records, hospital procurement signals, peer-reviewed literature, company filings, and vascular surgery registry information where available.
Primary validation is conducted through structured discussions with vascular surgeons, interventional radiologists, hospital procurement leaders, distributors, payers, and device. Findings are triangulated across clinical practice, commercial activity, reimbursement conditions, regulatory requirements, and macroeconomic indicators to ensure balanced, data-backed conclusions. AI-related insights are assessed through documented medical imaging use cases, regulatory trends, validated clinical workflow applications, and practical hospital integration relevance.
The stent grafts market is positioned for sustained relevance as healthcare systems continue to favor less invasive vascular repair, earlier diagnosis, and outcomes-based device selection. Demand is strongest where aging populations, imaging infrastructure, specialist expertise, clinical evidence, and reimbursement support align.
Future leadership will be determined by clinical durability, anatomical versatility, regulatory excellence, digital planning integration, quality assurance, and regional. Organizations that combine proven device performance with AI-supported workflows, strong physician partnerships, robust post-market surveillance, and resilient supply chains will be best placed to address demand across mature and emerging stent graft markets.