The global vascular access devices market is estimated to be valued at USD 8.75 Bn in 2025 and is expected to reach USD 14.24 Bn by 2032, exhibiting a compound annual growth rate (CAGR) of 7.2% from 2025 to 2032. This significant growth is driven by increasing demand for minimally invasive surgery, rising prevalence of chronic diseases requiring vascular access, and technological advancements enhancing device safety and efficacy across healthcare settings worldwide.
A prominent trend in the vascular access devices market is the integration of advanced materials and smart technologies to improve device performance and patient outcomes. Innovations such as antimicrobial coatings and ultrasound guided insertion techniques are reducing infection rates and procedural complications. Additionally, the growing adoption of home healthcare services and outpatient procedures is fueling demand for portable and user-friendly vascular access solutions, shaping market dynamics and encouraging continuous product development in the sector.
|
Current Events |
Description and its Impact |
|
U.S. FDA Approval of New Vascular Access Devices |
|
|
Technological Advancement in Catheter Materials |
|
Uncover macros and micros vetted on 75+ parameters: Get instant access to report
The central vascular access devices segment is projected to account for 63.9% of the market share in 2025, owing to the vitality of its use in controlling long-term and complicated intravenous therapies. Central Vascular Access Devices (CVADs) comprising of Peripherally Inserted Central Catheters (PICCs), Non-tunneled Catheters, Tunneled Catheters and Implantable Ports play a crucial role in critical care and oncology practice where patients need to receive medications, fluids or parenteral nutrition over a prolonged period.
In October 2024, Teleflex (TFX) announced the launch of two new devices in Canada, aimed at improving the PICC (Peripherally Inserted Central Catheters) insertion process and minimizing complications. The next-generation Arrow VPS Rhythm DLX Device and NaviCurve Stylet are designed to work together, offering vascular access professionals a more efficient and predictable method for PICC placement. These innovations were developed with feedback from industry-leading vascular access professionals.
The medication administration segment is expected to capture 45.5% share in 2025, because of the fact that intravenous drug delivery is a prerequisite in current medical application. This segment is the core of the demand because of the high need of administering various types of drugs such as antibiotics and chemotherapy agents, analgesics and fluids in acute care, oncology, critical illness, and chronic disease care. Since intravenous delivery of drugs offers a speedy and regulated delivery of the therapeutic agent, vascular access devices are the basis of ensuring the efficacy of treatment and patient safety.
The emergence of chronic diseases and steadily complicated treatment regimens necessitate consistent and dependable vascular access to administer medication, which has increased the use of device options that are customized to address a specific therapeutic requirement. As an example, drugs with irritating or vesicant effects would require central devices to avoid any tissue damage, and temporary treatment could be supported with peripheral intravenous catheters.
The hospitals and clinics segment is projected to hold 32.4% share in 2025, due to the role they play in providing acute care, complicated treatments, and emergency procedures. Such healthcare facilities need a number of vascular access points to cater to various patient types, including critically ill patients requiring continuous infusion and monitoring to surgical patients requiring fluid replacement and transfusion.
The accessibility of specialized personnel who have been trained on the use of vascular access devices on insertion, management and maintenance is also beneficial to hospitals and clinics as more people will use more advanced devices like central lines and implantable ports. Also affecting the choice of such facilities is the availability of resources to ultrasound-guidance and tip-placement technologies that can boost the success of the procedure and minimize risks such as infections and thrombosis.

To learn more about this report, Download Free Sample
The North America region is projected to lead the market with a 38.3% share in 2025, led by established healthcare ecosystem with high spending on medical infrastructure, high medical spending and large concentration of major medical device manufacturers. Also, North America has strong reimbursement systems that are motivating hospitals and clinics to invest in new vascular access technology. The presence of such industry giants like Becton Dickinson and Company, Medtronic plc and Smiths Medical has a heavy presence here and they are contributing to the scene through constant product innovations and strategic acquisitions.
In November 2024, Xeltis announced that the U.S. FDA granted Breakthrough Device designation for its aXess vascular access conduit, and the first patient was enrolled in the aXess staged pivotal trial in the United States. The aXess device is designed to create a new, permanent, living vessel for hemodialysis vascular access. Xeltis, based in Eindhoven, the Netherlands, stated that the procedure was performed by vascular surgeon Dr. Karl Illig at the Flow Vascular Institute in Texas, U.S.
The vascular access devices market in the Asia Pacific region is projected to account for 24.3% in 2025, driven by the development of healthcare infrastructure, the rising prevalence of chronic illnesses, and increased awareness of minimally invasive procedures. The governments in the region and more so in China and India are on a frenzy in modernizing their health care systems and in opening their markets to foreign and domestic firms by creating a lighter regulatory ride.
In November 2021, Zylox-Tonbridge Medical Technology Co., Ltd. announced a strategic partnership with Guangdong Hicicare Science Co., Ltd. to co-develop and accelerate the commercialization of vascular guidewire products in China. The collaboration aims to introduce the "Zylox-Hicicare Guidewire Family" for peripheral vascular interventions and the Beidou series micro guidewires for neurovascular procedures.
U.S. vascular access devices market is a worldwide leader in terms of advanced healthcare system and patient awareness. Large corporations like Becton Dickinson and Medtronic are very active in R&D in this area, leading to innovations in catheter design, safety engineered devices, and infection prevention technologies. Favorable regulation by U.S. FDA and a broad-based reimbursement climate encourages rapid product adoption. Vascular access solutions are also in high demand in the U.S., which has a large network of hospitals and outpatient facilities that need them to perform various kinds of medical procedures.
In November 2023, BD (Becton, Dickinson and Company), a leading global medical technology company, launched the SiteRite 9 Ultrasound System, an advanced tool designed to improve clinician efficiency in placing vascular access devices such as PICCs, central venous catheters, and IV lines. The system features a 15.6-inch touch screen with enhanced image quality, providing industry-leading tools for catheter placement
Germany remains vascular access devices market leader in Europe with a highly developed infrastructure in hospitals and insistence on the quality of healthcare provision. The nation has many major players in the industry including B. Braun and Fresenius that have been central in producing and exporting vascular access technologies in Europe and other parts of the world. The healthcare policies of Germany focus on patient safety and innovation, and the next-generation vascular devices should be integrated easily. Also, it has strategic central positioning in Europe that facilitates effective logistics and trade in this region and improves market forces.
In February 2025, Cagent Vascular, Inc. launched its Serranator SL-Pro PTA serration balloon catheter for chronic limb-threatening ischemia and pedal disease. The FDA-cleared device uses proprietary serration technology for improved vessel dilation and trackability. Dr. Michael Lichtenberg of the Arnsberg Clinic in Germany highlighted its low complication rate and effectiveness in treating complex diseases, especially in pedal arteries.
The market of the vascular access device in China is growing fast due to the government efforts to enhance healthcare access and infrastructure development particularly in tier 2 and 3 cities. Demand is driven by the rising population of the aging population and surge in numbers of chronic ailments that necessitate vascular procedures. The multinational corporations such as Terumo Corporation and Boston Scientific have developed strong business networks by forming partnerships and manufacturing within the country.
In November 2021, Shanghai Bluevastec MedTech Co., Ltd. (Bluevastec) announced that its Vflower Venous Stent System gained access to China’s ‘Green Path’ for innovative medical devices. The stent features a unique design for better flexibility and support, offering a variable diameter and precise positioning. This approval accelerates its market launch in China, where venous stents are limited. The device’s clinical trial showed a 100% success rate and is praised for its long-term performance.
India vascular access devices market is characterized by tremendous growth potential driven by rising healthcare expenditure, increased urbanization, and growing incidence of lifestyle-related diseases. Government programs aimed at expanding healthcare coverage and affordability have improved healthcare access for large population segments. Major international players including Becton Dickinson collaborate with Indian distributors and hospitals, while domestic manufacturers focus on affordable product lines suited to the cost-sensitive market.
In May 2025, S3V Vascular Technologies received financial support from the Technology Development Board (TDB) to establish India’s first integrated manufacturing plant for mechanical thrombectomy kits. The plant, located in Chennai, will produce neuro-intervention devices locally, reducing reliance on imports and making stroke care more affordable. The project aims to target the $2 billion domestic market and expand globally with CE and U.S. FDA approvals.

To learn more about this report, Download Free Sample
| Report Coverage | Details | ||
|---|---|---|---|
| Base Year: | 2024 | Market Size in 2025: | USD 8.75 Bn |
| Historical Data for: | 2020 To 2024 | Forecast Period: | 2025 To 2032 |
| Forecast Period 2025 to 2032 CAGR: | 7.2% | 2032 Value Projection: | USD 14.24 Bn |
| Geographies covered: |
|
||
| Segments covered: |
|
||
| Companies covered: |
Becton, Dickinson and Company, Teleflex Incorporated, B. Braun SE, ICU Medical, Inc., Medtronic plc, AngioDynamics, Inc., Terumo Corporation, Nipro Corporation, Fresenius Medical Care AG & Co. KGaA, Cook Medical, Merit Medical Systems, Inc., Access Vascular, Inc., Vygon Group, Cardinal Health, Inc., and Argon Medical Devices, Inc. |
||
| Growth Drivers: |
|
||
| Restraints & Challenges: |
|
||
Uncover macros and micros vetted on 75+ parameters: Get instant access to report

To learn more about this report, Download Free Sample
The increasing prevalence of chronic illnesses like diabetes, cancer, and cardiovascular disorders is really driving the need of vascular access devices in the world. Patients with these disorders often need prolonged intravenous treatments, e.g. chemotherapy, dialysis, parenteral nutrition, and drug delivery, which require stable and safe vascular access. With the chronic illnesses becoming a significant burden to the healthcare systems, the demands of gadgets like central venous catheters, Peripherally Inserted Central Catheters (PICCs), and hemodialysis catheters have shot up. In addition, new medical therapies and prolonged patient survival have complicated and prolonged the treatment procedures further highlighting the significance of maintaining vascular access.
According to WHO, on September 25, 2025, the prevalence of chronic conditions among young people has risen significantly over the past 20 years. Nearly 30% of children and young adults aged 5 to 25 are now living with conditions like ADHD, autism, asthma, prediabetes, and depression. This increase is particularly high among those from lower socioeconomic backgrounds. A recent study based on data from the National Health Interview Survey (1999-2018) shows a steady annual rise in chronic conditions, with an estimated 130,000 additional children and 80,000 young adults affected each year. These conditions are treatable with access to quality healthcare, but disparities in the U.S. health system hinder proper care.
The increasing popularity of home healthcare services is an eye opener to the international market of vascular access devices. With the global healthcare system focusing more and more on cost-efficiency and patient-centered care, the transition of the old-fashioned hospitals to the home-based care is gaining momentum. This is especially true in the areas of chronic disease management, oncology and intravenous therapies (over a long period of time) where frequent visits to the hospital are costly to the patient and the medical infrastructure. Vascular access devices, including peripheral intravenous catheters, midline catheters, and Peripherally Inserted Central Catheters (PICCs) are important in providing safe and reliable access to the vascular system to administer medications, nutrition, and other intravenous therapy at home.
In June 2025, Vellum Health, a mobile healthcare platform providing advanced intravenous (IV) services at the bedside, announced the successful close of its Series A funding round, led by FCA Venture Partners with participation from Green Park & Golf Ventures. The company also unveiled its new brand, Vellum Health, which integrates a portfolio of acquired vascular access companies into a unified tech-enabled care delivery platform. Vellum Health offers mobile IV access, infusion therapy, and on-site transfusion services, expanding home healthcare services by bringing high-quality care directly to patients in skilled nursing facilities, long-term acute care centers, and homes.
Share
Share
About Author
Komal Dighe is a Management Consultant with over 8 years of experience in market research and consulting. She excels in managing and delivering high-quality insights and solutions in Health-tech Consulting reports. Her expertise encompasses conducting both primary and secondary research, effectively addressing client requirements, and excelling in market estimation and forecast. Her comprehensive approach ensures that clients receive thorough and accurate analyses, enabling them to make informed decisions and capitalize on market opportunities.
Missing comfort of reading report in your local language? Find your preferred language :
Transform your Strategy with Exclusive Trending Reports :
Frequently Asked Questions
Joining thousands of companies around the world committed to making the Excellent Business Solutions.
View All Our Clients