Uterine Fibroid Treatment Devices

Global Uterine Fibroid Treatment Devices Market to Reach US$8.1 Billion by 2030

The global market for Uterine Fibroid Treatment Devices estimated at US$5.3 Billion in the year 2024, is expected to reach US$8.1 Billion by 2030, growing at a CAGR of 7.4% over the analysis period 2024-2030. Surgical, one of the segments analyzed in the report, is expected to record a 8.7% CAGR and reach US$5.3 Billion by the end of the analysis period. Growth in the Ablation segment is estimated at 5.1% CAGR over the analysis period.

The U.S. Market is Estimated at US$1.4 Billion While China is Forecast to Grow at 11.8% CAGR

The Uterine Fibroid Treatment Devices market in the U.S. is estimated at US$1.4 Billion in the year 2024. China, the world`s second largest economy, is forecast to reach a projected market size of US$1.7 Billion by the year 2030 trailing a CAGR of 11.8% over the analysis period 2024-2030. Among the other noteworthy geographic markets are Japan and Canada, each forecast to grow at a CAGR of 3.6% and 7.2% respectively over the analysis period. Within Europe, Germany is forecast to grow at approximately 4.9% CAGR.

Global "Uterine Fibroid Treatment Devices" Market – Key Trends & Drivers Summarized

Why Is There a Rising Demand for Advanced Uterine Fibroid Treatments?
The global burden of uterine fibroids—benign tumors of the uterus—has grown substantially, affecting up to 70–80% of women by the age of 50, with symptomatic cases leading to heavy bleeding, pelvic pain, infertility, and other complications. This rising incidence is directly influencing the demand for effective, less invasive treatment modalities, particularly in reproductive-age women who seek uterine-sparing procedures. Historically, hysterectomy was the dominant treatment; however, patient preference is increasingly shifting toward uterus-preserving alternatives such as myomectomy, uterine artery embolization (UAE), and minimally invasive surgeries like laparoscopic and robotic-assisted interventions. The stigma and social implications of undergoing hysterectomy—especially in cultures where fertility is highly valued—are reinforcing this transition. In addition, lifestyle changes, late pregnancies, and obesity have been identified as risk-enhancing factors, leading to earlier diagnosis and treatment. The healthcare industry’s increased focus on women’s health and a surge in screening and diagnostic rates, due in part to better awareness campaigns, are further propelling the market for uterine fibroid treatment devices.

How Are Technology and Innovation Redefining Treatment Modalities?
Innovative breakthroughs are at the heart of the evolution in uterine fibroid management, with medical device manufacturers introducing cutting-edge equipment designed to improve clinical outcomes, shorten recovery periods, and reduce surgical complications. Technologies such as high-intensity focused ultrasound (HIFU), radiofrequency ablation (RFA), and MRI-guided focused ultrasound surgery (MRgFUS) are redefining non-invasive or minimally invasive treatment approaches. These devices enable precise targeting of fibroids without damaging surrounding tissues, offering patients rapid relief with fewer side effects and outpatient-level convenience. Additionally, laparoscopic power morcellators and advanced hysteroscopic tools are being refined to improve safety, especially in light of past concerns around tissue dissemination. Robotic surgical systems, though expensive, are increasingly employed in tertiary care hospitals to improve accuracy in complex fibroid removal. These technological advancements are not only increasing physician confidence but are also expanding treatment availability to lower-tier hospitals and outpatient clinics, democratizing access to quality care.

What Are Healthcare Systems and Providers Doing to Expand Access?
Access to fibroid treatment is being shaped by a combination of policy efforts, insurance coverage reforms, and evolving clinical guidelines. In high-income countries, broader insurance inclusion of less invasive and outpatient procedures has helped bring down costs and improve uptake. Many governments and private providers are now classifying uterine fibroid treatments as part of essential women’s healthcare, leading to better diagnosis, referral, and subsidization processes. At the same time, low- and middle-income countries (LMICs) are catching up, with investments in mobile diagnostic units, training programs for gynecologic surgeons, and public health campaigns aimed at raising awareness. Multinational NGOs and global health organizations are also contributing to capacity building by funding medical missions and donating devices to rural hospitals. Furthermore, hospitals are integrating multidisciplinary fibroid clinics combining gynecology, radiology, and pain management to offer holistic care, ensuring that patients receive tailored, evidence-based treatment options. The shift toward outpatient care and same-day discharge protocols is also optimizing hospital resources and reducing patient burden.

What’s Driving the Escalating Growth in the Uterine Fibroid Treatment Devices Market?
The growth in the uterine fibroid treatment devices market is driven by several factors closely linked to technology evolution, clinical practices, and patient preferences. The widespread availability of non-invasive and minimally invasive devices is dramatically shifting treatment patterns away from traditional open surgery, attracting a larger volume of patients seeking faster recovery and fertility preservation. The expanding pool of diagnosed cases—due to improved imaging techniques like transvaginal ultrasound and MRI—is also increasing procedural volumes. Patient behavior is playing a pivotal role; as awareness about fibroids rises, women are actively seeking early intervention and alternatives to hysterectomy. Additionally, private and public healthcare providers are increasingly investing in device-based fibroid treatments due to their procedural efficiency and favorable cost-benefit ratios. The increasing presence of outpatient and ambulatory surgery centers, particularly in North America and parts of Asia-Pacific, is expanding the commercial viability of newer treatment devices. Rising healthcare spending, demographic shifts such as delayed childbirth, and higher incidences of obesity and hormonal disorders are further fueling demand. Together, these factors form a robust and multifaceted foundation for sustained market expansion in the years ahead.

SCOPE OF STUDY:

The report analyzes the Uterine Fibroid Treatment Devices market in terms of units by the following Segments, and Geographic Regions/Countries:

Segments:
Technology (Surgical, Ablation); Mode of Treatment (Invasive, Minimally Invasive, Non-Invasive)

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 42 Featured) -

• AbbVie Inc.
• Boston Scientific Corporation
• CONMED Corporation
• CooperSurgical Inc.
• Ethicon, Inc.
• Gynesonics
• Hologic, Inc.
• INSIGHTEC Ltd.
• Karl Storz SE & Co. KG
• Lumenis Be Ltd.
• Medtronic plc
• Merit Medical Systems, Inc.
• Minerva Surgical, Inc.
• Myovant Sciences GmbH
• ObsEva SA
• Olympus Corporation
• Philips Healthcare
• Profound Medical Corp.
• Siemens Healthineers AG
• Stryker Corporation

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