Welcome to our dedicated page for Merit Med Sys news (Ticker: MMSI), a resource for investors and traders seeking the latest updates and insights on Merit Med Sys stock.
Merit Medical Systems, Inc. (NASDAQ: MMSI) delivers essential updates for stakeholders tracking innovations in minimally invasive medical devices. This dedicated news hub provides verified information about the company's advancements in cardiology, radiology, and vascular access technologies.
Investors and healthcare professionals will find timely updates on regulatory milestones, product launches, and strategic initiatives. Our curated collection includes earnings reports, clinical trial developments, and partnership announcements that shape Merit Medical's position in the $450B+ global medical device market.
Key coverage areas include new FDA clearances for diagnostic catheters, financial performance across international markets, and innovations in embolization technologies. All content undergoes strict verification to ensure compliance with financial reporting standards and medical industry regulations.
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Merit Medical Systems (NASDAQ: MMSI) has announced the enrollment of the first patient in its WRAP North America registry study at Bluff City Vascular in Memphis, TN. The registry will evaluate the real-world safety and effectiveness of the WRAPSODY Cell-Impermeable Endoprosthesis (CIE), a device designed to restore vascular access in hemodialysis patients.
The study aims to enroll up to 250 patients across the US and Canada, following them for three years. This registry complements the ongoing WRAP Global registry, which targets 500 non-North American patients. The WRAPSODY CIE received FDA approval in December 2024 and Health Canada approval in April 2025, following earlier approvals in the EU and Brazil.
Merit Medical Systems (NASDAQ: MMSI) has launched the Prelude Wave™ Hydrophilic Sheath Introducer with SnapFix™ Securement Technology in the US market. This innovative medical device offers significant improvements over competing products, including twice the lubricity, twice the resistance to buckling and kinking, and 40% less insertion force.
The device addresses critical challenges in radial access procedures, where radial artery spasm occurs in up to 20% of patients and arterial occlusion affects approximately 4.6% of cases. The SnapFix technology provides twice the adhesive strength compared to leading competitors, with superior physician ratings for performance and ease of use.
Merit Medical Systems (NASDAQ:MMSI) reported strong Q2 2025 financial results, with revenue reaching $382.5 million, up 13.2% year-over-year. The company demonstrated solid performance with constant currency revenue growth of 12.5% and organic growth of 6.7%. Notable metrics include non-GAAP EPS of $1.01 (up 9.8%) and free cash flow generation of $89.1 million in H1 2025.
The company has raised its full-year 2025 guidance, now expecting revenue between $1.495-$1.507 billion (10-11% growth) and non-GAAP EPS of $3.52-$3.72. Additionally, Merit announced the acquisition of Biolife, a hemostatic devices manufacturer, and appointed Martha Aronson as new President and CEO, effective October 3, 2025.
Merit Medical Systems (NASDAQ: MMSI) has appointed Martha Aronson as its new President and CEO, effective October 3, 2025. Founder Fred Lampropoulos will transition from his current role as President and CEO to continue serving as Chairman of the Board. Aronson brings extensive healthcare experience, having managed global businesses worth $500M-$1B at companies including Ecolab and Hill-Rom.
Additionally, Merit announced preliminary Q2 2025 revenue of $380-384 million, representing a 12-14% increase year-over-year. On a constant currency basis, revenue grew 11-13%. The company will release complete Q2 2025 financial results on July 30, 2025.
Merit Medical Systems (NASDAQ: MMSI), a leading healthcare technology manufacturer, has scheduled its second quarter 2025 financial results announcement for July 30, 2025, after market close. The company will host an investor conference call the same day at 5:00 p.m. Eastern Time.
Founded in 1987, Merit Medical specializes in proprietary medical devices for interventional, diagnostic, and therapeutic procedures, particularly in cardiology, radiology, oncology, critical care, and endoscopy. The company maintains a global presence with over 800 sales and clinical support professionals and approximately 7,300 employees worldwide.
Merit Medical Systems (NASDAQ: MMSI) has announced 12-month efficacy results for its WRAPSODY Cell-Impermeable Endoprosthesis (CIE) device from the single-arm arteriovenous graft (AVG) cohort of the WAVE trial. The study included 112 patients with AVG treated with WRAPSODY CIE.
Key findings include:
- 6-month target lesion primary patency (TLPP) of 81.4%, exceeding the performance goal of 60% by 21.4 percentage points
- 12-month TLPP of 60.2%
- Access circuit primary patency (ACPP) at 6 and 12 months were 69.2% and 36.2% respectively
- 95.4% of patients were free from adverse events, surpassing the safety goal of 89.0%
The WRAPSODY CIE is currently available in Brazil, the European Union, and is approved for commercial distribution in the United States.
Merit Medical Systems (MMSI) reported strong Q1 2025 financial results with revenue reaching $355.4 million, up 9.8% year-over-year. The company demonstrated solid performance with constant currency revenue growth of 10.9% and organic growth of 6.0%.
Key financial metrics include GAAP operating margin of 11.5% (up from 11.1%), non-GAAP operating margin of 19.3% (up from 17.0%), and GAAP EPS of $0.49 (up 2.0%). Non-GAAP EPS increased 14.8% to $0.86.
The company maintained its 2025 revenue guidance of $1.470-$1.490 billion but updated its non-GAAP EPS guidance to $3.29-$3.42, reflecting strong Q1 results offset by impacts from recent trade policies. As of March 31, 2025, Merit had cash and cash equivalents of $395.5 million and total debt of $747.5 million.
Merit Medical Systems (NASDAQ: MMSI) has announced the US commercial launch of its Ventrax™ Delivery System, the latest addition to its electrophysiology and cardiac rhythm management portfolio. The system is designed to facilitate ablation procedures for treating ventricular tachycardia (VT), a condition contributing to approximately 75% of sudden cardiac deaths in the US.
The Ventrax system features a 95-cm sheath for targeted access, ultralow-profile transition between sheath and pigtail-dilator, and an angled tip to enhance ablation catheter reach. It provides retrograde aortic access, offering improved access to certain ventricle areas compared to traditional methods.
Key medical experts from Duke Health, including Dr. Albert Sun and Dr. Jason Koontz, contributed to the system's development. The device addresses a growing need in VT ablation procedures, which represent one of the fastest-growing areas in electrophysiology.