PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2123579
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2123579
According to Mordor Intelligence, the global transcatheter pulmonary valve market size was valued at USD 77.76 million in 2025 and estimated to grow from USD 82.03 million in 2026 to reach USD 107.23 million by 2031, at a CAGR of 5.49% during the forecast period (2026-2031).

This report is Segmented by Technology (Balloon-Expanded Valve and Self-Expanded Valve), Application (Pulmonary Stenosis, Pulmonary Regurgitation, and More), End-User (Pediatric Hospitals, Pulmonary Regurgitation, and More), RVOT Anatomy (Conduit-Based RVOT and Native / Enlarged RVOT), and Geography (North America, Europe, and More). The Market Forecasts are Provided in Terms of Value (USD).
Adults living with congenital heart defects now exceed 1 million in the United States, 20% of whom require complex cardiac re-interventions. Hospitalizations are 91% higher and average USD 81,332 per stay versus USD 49,000 for non-congenital heart failure, incentivizing payers to endorse less invasive options. Strong long-term tissue durability-99.3% freedom from structural deterioration over eight years-supports device longevity expectations. The demographic trajectory ensures persistent case flow across developed markets.
Multicenter registry data covering 243 U.S. patients recorded 98% acceptable hemodynamics and 99% freedom from major composite events at one-year follow-up. UK regulators granted exceptional approval for the Venus P-valve despite a pending CE mark, signaling readiness to fast-track solutions addressing unmet needs. Ability to land securely in large native RVOT anatomies effectively doubles the clinical universe.
FDA registries logged 631 adverse events for Melody implants, including stent fragment embolization. Ten-year freedom from dysfunction sits at 53% in pediatric cohorts, driving regulatory calls for harmonized durability definitions. Although RESILIA tissue shows encouraging eight-year durability, pulmonary positioning evidence remains early stage.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Global revenue remains anchored by balloon-expandable devices, which commanded 57.62% of the transcatheter pulmonary valve market share in 2025. Precise conduit sizing, immediate anchoring, and robust long-term data sustain clinician confidence. The Edwards SAPIEN 3 system achieved 98.1% device success and 100% freedom from surgical reintervention at one year. At the same time, self-expanding solutions are advancing at 11.92% CAGR through 2031, transforming therapeutic possibilities for enlarged native RVOT anatomies. One-year registry follow-up showed 96% freedom from composite events with acceptable hemodynamics in 98% of cases. The Venus P-valve and Harmony systems now anchor treatment algorithms in Asia and North America respectively, with CE certification further broadening access.
Pulmonary regurgitation generated 45.02% of 2025 procedure volume, reflecting historical focus on volume-overload correction. Nonetheless, pulmonary stenosis indications are forecast to post a 10.67% CAGR, the strongest trajectory within the transcatheter pulmonary valve market. Earlier intervention strategies that aim to pre-empt right-ventricular compromise underpin this acceleration, especially for repaired Tetralogy of Fallot patients. Comparative trials such as COMPASS will clarify optimal timing and modality selection, potentially increasing stenosis-related volumes.
North America generated 38.30% of global revenue in 2025, buoyed by advanced centers, widespread payer support, and active clinical-trial pipelines. CMS's 2.9% outpatient payment hike and new device categories accelerate catheter-lab uptake. Canada and Mexico are scaling specialist capabilities, supported by cross-border training and regional clinical studies.
Europe sustains mid-single-digit growth, underpinned by mature infrastructure and adaptable regulators willing to expedite devices with demonstrable need. Exceptional UK approval of Venus P-valve underscores demand-driven flexibility. Health-economic studies from Spain showed favorable EUR 6,952 per QALY, reinforcing payer confidence.
Asia-Pacific represents the fastest regional expansion at 10.44% CAGR. Domestic innovators such as Venus Medtech tailor self-expanding valves for prevalent anatomical features in Chinese and Indian populations. Japan's registry exceeding 8,000 transcatheter aortic cases provides a procedural blueprint for pulmonary adoption. Government initiatives to expand cardiac catheterization labs in South Korea and Australia further catalyze uptake.
South America and the Middle East & Africa trail but show rising interest as referral pathways mature. Partnerships with global device makers and training exchanges with European centers are improving procedural readiness. Incremental gains in reimbursement coverage, especially for pediatric CHD, are expected to translate into a steady but smaller share of the transcatheter pulmonary valve market by 2030.