Abdominal Aortic Aneurysm (AAA) Repair Device

Global Abdominal Aortic Aneurysm (AAA) Repair Device Market to Reach US$3.5 Billion by 2030

The global market for Abdominal Aortic Aneurysm (AAA) Repair Device estimated at US$2.6 Billion in the year 2024, is expected to reach US$3.5 Billion by 2030, growing at a CAGR of 5.5% over the analysis period 2024-2030. Endovascular Stent Graft Systems, one of the segments analyzed in the report, is expected to record a 6.4% CAGR and reach US$2.4 Billion by the end of the analysis period. Growth in the Synthetic Graft Systems segment is estimated at 3.6% CAGR over the analysis period.

The U.S. Market is Estimated at US$696.2 Million While China is Forecast to Grow at 8.8% CAGR

The Abdominal Aortic Aneurysm (AAA) Repair Device market in the U.S. is estimated at US$696.2 Million in the year 2024. China, the world`s second largest economy, is forecast to reach a projected market size of US$712.0 Million by the year 2030 trailing a CAGR of 8.8% over the analysis period 2024-2030. Among the other noteworthy geographic markets are Japan and Canada, each forecast to grow at a CAGR of 2.6% and 5.5% respectively over the analysis period. Within Europe, Germany is forecast to grow at approximately 3.6% CAGR.

Global Abdominal Aortic Aneurysm (AAA) Repair Device Market – Key Trends & Drivers Summarized

Why Are AAA Repair Devices Central to Managing Aneurysmal Disease and Improving Vascular Outcomes?
Abdominal Aortic Aneurysm (AAA) repair devices are vital in treating the life-threatening dilation of the abdominal aorta, a condition that can lead to catastrophic rupture if left unaddressed. These devices—primarily comprising endovascular stent graft systems and surgical grafts—are designed to reinforce the weakened arterial wall, redirect blood flow, and prevent further aneurysmal expansion. Their role in vascular surgery has become increasingly critical as aging populations, improved diagnostics, and screening programs drive earlier detection and intervention.

Endovascular Aneurysm Repair (EVAR), a minimally invasive alternative to open surgery, has become the dominant mode of treatment due to reduced operative risk, shorter recovery times, and lower morbidity. Technological refinements in stent graft flexibility, seal integrity, and anatomical adaptability have expanded the eligible patient pool, allowing for customized solutions even in complex or tortuous vascular anatomies.

How Are Device Innovations Enhancing Safety, Precision, and Patient Eligibility in AAA Repair?
Modern AAA repair devices are incorporating advanced materials, low-profile delivery systems, and modular components to improve navigability and precision placement within the aorta. Innovations such as fenestrated and branched stent grafts are enabling treatment of patients with challenging proximal neck anatomies or involvement of branch vessels. Additionally, polymer-based sealing technologies and repositionable grafts are increasing procedural control and reducing the risk of endoleaks.

Real-time imaging integration, 3D navigation tools, and AI-driven procedural planning are further optimizing outcomes by allowing for better intraoperative visualization and device alignment. These capabilities are enhancing procedural efficiency and minimizing post-operative complications, leading to growing clinical acceptance and broader adoption in both high-volume centers and regional hospitals.

Which Patient Segments and Regional Healthcare Systems Are Driving Demand for AAA Repair Devices?
AAA repair devices are primarily used in patients aged 65 and older, with prevalence higher among males, smokers, and individuals with hypertension or atherosclerosis. Elective repair in asymptomatic patients is increasing due to improved screening efforts in high-risk populations. Emergency use in rupture cases, while less frequent, continues to be a critical application requiring rapid deployment and robust device performance.

North America and Europe lead in market adoption, supported by established screening guidelines, reimbursement coverage, and widespread availability of EVAR expertise. Asia-Pacific is experiencing rising demand as demographic aging, improving healthcare access, and government-led vascular screening initiatives expand the patient base. Emerging markets in Latin America and the Middle East are also adopting AAA repair technologies, driven by growing investments in vascular care infrastructure and surgeon training.

How Are Reimbursement Models, Regulatory Pathways, and Long-Term Surveillance Influencing Market Evolution?
Regulatory frameworks in key markets continue to shape the pace of innovation and commercialization. While FDA and CE approvals have set rigorous performance benchmarks, post-market surveillance is becoming increasingly important to monitor device durability, migration risks, and secondary interventions. Reimbursement systems play a crucial role in adoption, particularly for newer technologies such as fenestrated and branched grafts, which command higher procedural costs.

Healthcare systems are under pressure to balance upfront costs with long-term value, pushing manufacturers to generate robust real-world evidence, including data on patient quality of life, reintervention rates, and health economics. Device lifecycle management and remote monitoring capabilities are gaining attention as stakeholders emphasize outcome-driven care and cost-efficiency in vascular treatment pathways.

What Are the Factors Driving Growth in the AAA Repair Device Market?
The AAA repair device market is expanding due to rising detection rates, increasing procedural volumes, and continued innovation in endovascular solutions. Clinical demand is reinforced by the aging global population, growing awareness among referring physicians, and improved device accessibility in non-metropolitan healthcare settings. As device design advances and imaging-guided procedures become more precise, the boundaries of treatable cases are being pushed wider.

Looking ahead, the market’s trajectory will depend on how effectively stakeholders balance innovation, clinical risk, and economic value in an increasingly outcomes-focused healthcare landscape. As patient expectations and surgical capabilities continue to evolve, could next-generation AAA repair devices redefine the standard of care in complex vascular disease management?

SCOPE OF STUDY:

The report analyzes the Abdominal Aortic Aneurysm (AAA) Repair Device market in terms of units by the following Segments, and Geographic Regions/Countries:

Segments:
Product Type (Endovascular Stent Graft Systems, Synthetic Graft Systems); Anatomy (Traditional Anatomy, Complex Anatomy); Site (Infrarenal AAA, Pararenal AAA)

Geographic Regions/Countries:
World; United States; Canada; Japan; China; Europe (France; Germany; Italy; United Kingdom; Spain; Russia; and Rest of Europe); Asia-Pacific (Australia; India; South Korea; and Rest of Asia-Pacific); Latin America (Argentina; Brazil; Mexico; and Rest of Latin America); Middle East (Iran; Israel; Saudi Arabia; United Arab Emirates; and Rest of Middle East); and Africa.

Select Competitors (Total 36 Featured) -

• Abbott Laboratories
• Abiomed Inc.
• Artivion Inc. (formerly CryoLife)
• B. Braun Melsungen AG
• Bentley InnoMed GmbH
• BiFlow Medical
• Bolton Medical Inc.
• Boston Scientific Corporation
• Braile Biomedica
• Cardiatis S.A.
• Cardinal Health Inc.
• Cook Medical Inc.
• Cordis Corporation
• Cytograft Tissue Engineering Inc.
• Endologix LLC
• Endospan Ltd.
• Fuji Systems Co., Ltd.
• Getinge AB (Maquet)
• Gore Medical (W. L. Gore & Associates)
• Grikin Advanced Materials Co., Ltd.

TARIFF IMPACT FACTOR

Our new release incorporates impact of tariffs on geographical markets as we predict a shift in competitiveness of companies based on HQ country, manufacturing base, exports and imports (finished goods and OEM). This intricate and multifaceted market reality will impact competitors by artificially increasing the COGS, reducing profitability, reconfiguring supply chains, amongst other micro and macro market dynamics.

We are diligently following expert opinions of leading Chief Economists (14,949), Think Tanks (62), Trade & Industry bodies (171) worldwide, as they assess impact and address new market realities for their ecosystems. Experts and economists from every major country are tracked for their opinions on tariffs and how they will impact their countries.

We expect this chaos to play out over the next 2-3 months and a new world order is established with more clarity. We are tracking these developments on a real time basis.

As we release this report, U.S. Trade Representatives are pushing their counterparts in 183 countries for an early closure to bilateral tariff negotiations. Most of the major trading partners also have initiated trade agreements with other key trading nations, outside of those in the works with the United States. We are tracking such secondary fallouts as supply chains shift.

To our valued clients, we say, we have your back. We will present a simplified market reassessment by incorporating these changes!

APRIL 2025: NEGOTIATION PHASE

Our April release addresses the impact of tariffs on the overall global market and presents market adjustments by geography. Our trajectories are based on historic data and evolving market impacting factors.

JULY 2025 FINAL TARIFF RESET

Complimentary Update: Our clients will also receive a complimentary update in July after a final reset is announced between nations. The final updated version incorporates clearly defined Tariff Impact Analyses.

Reciprocal and Bilateral Trade & Tariff Impact Analyses:

USA
CHINA
MEXICO
CANADA
EU
JAPAN
INDIA
176 OTHER COUNTRIES.

Leading Economists - Our knowledge base tracks 14,949 economists including a select group of most influential Chief Economists of nations, think tanks, trade and industry bodies, big enterprises, and domain experts who are sharing views on the fallout of this unprecedented paradigm shift in the global econometric landscape. Most of our 16,491+ reports have incorporated this two-stage release schedule based on milestones.

Please note: Reports are sold as single-site single-user licenses. Electronic versions require 24-48 hours as each copy is customized to the client with digital controls and custom watermarks. The Publisher uses digital controls protecting against copying and printing is restricted to one full copy to be used at the same location.

The latest version of Adobe Acrobat Reader is required to view the report. Upon ordering an electronic version, the Publisher will provide a link to download the purchased report.

Prior to fulfillment of an order, the client will be required to sign a document detailing the purchase terms for a publication from this publisher.