Welcome to our dedicated page for Medtronic news (Ticker: MDT), a resource for investors and traders seeking the latest updates and insights on Medtronic stock.
Medtronic plc (NYSE: MDT) is a Galway, Ireland-based healthcare technology company whose news flow reflects its broad activity in medical devices, diabetes technology, surgical robotics, and cardiovascular therapies. Company announcements frequently highlight regulatory milestones, clinical evidence, product launches, capital markets activity, and corporate governance developments that matter to investors and healthcare professionals following MDT stock.
Recent news has featured U.S. Food and Drug Administration clearances for key technologies, including the Hugo robotic-assisted surgery (RAS) system for urologic procedures and the MiniMed Go Smart Multiple Daily Injection (MDI) system, which connects the InPen smart insulin pen and the Instinct sensor made by Abbott through the MiniMed Go app. Medtronic has also reported on the broad U.S. commercial launch of the MiniMed 780G automated insulin delivery system integrated with the Instinct sensor, expanding its diabetes technology ecosystem.
Investors can also track Medtronic’s cardiovascular and hypertension-related developments, such as the final National Coverage Determination from the U.S. Centers for Medicare & Medicaid Services for the Symplicity Spyral renal denervation system, and updates on growth drivers like pulsed field ablation and other cardiovascular therapies discussed in earnings releases. Financial news includes quarterly earnings reports, guidance updates, dividend declarations, and details of senior notes offerings and redemptions.
This MDT news page aggregates coverage of topics including diabetes business developments (such as the planned MiniMed IPO registration), conference presentations, leadership and board changes, and major clinical or reimbursement milestones. Readers interested in Medtronic’s role in chronic disease management, minimally invasive surgery, and global healthcare technology can use this page to follow ongoing announcements and review the company’s evolving strategic priorities over time.
Medtronic (NYSE:MDT) has secured CE Mark approval for expanded indications of its MiniMed™ 780G system, now authorized for use in children as young as 2 years old, pregnant women, and type 2 diabetes patients in Europe.
Clinical data showed significant benefits across all new indications: The LENNY trial demonstrated a 0.6% lower HbA1C and 9.9% higher time in range in children aged 2-6 years. For pregnant women, the system achieved an average Pregnancy Time in Range of 66.5%. In type 2 diabetes patients, trials showed a 0.7% reduction in HbA1c and increased time in range to 80%.
The company is currently seeking FDA approval for type 2 diabetes indication in the U.S. and conducting clinical trials for use in young children.
Medtronic (NYSE:MDT) has appointed Chad Spooner as Chief Financial Officer of MiniMed, effective July 14, 2025, ahead of its planned separation into an independent public company. Spooner brings over 25 years of financial leadership experience, most recently serving as CFO at BIC.
The appointment comes as Medtronic prepares to spin off its diabetes business under the MiniMed name within 18 months of the initial announcement. MiniMed focuses on transforming diabetes care for patients with type 1 and type 2 diabetes requiring daily insulin injections. The separation will be executed through a series of capital markets transactions, subject to customary conditions and legal requirements.
Medtronic (NYSE:MDT) has appointed Dr. Joon Lee, CEO of Emory Healthcare, to its Board of Directors as an independent director, effective June 18, 2025. Dr. Lee, who will serve on the Science and Technology Committee and Compensation and Talent Committee, brings over 25 years of healthcare leadership experience.
Currently leading Emory Healthcare's $7.7B healthcare system with 12 hospitals and 29,000+ employees, Dr. Lee previously held executive positions at UPMC, including Executive VP and President of Physician Services. He also served as CMO of UPMC Insurance Services, managing a $13B health insurance division. His expertise spans interventional cardiology, clinical research, and healthcare technology.
Medtronic (NYSE: MDT) announced its participation in Bernstein's 41st Strategic Decisions Conference on May 29, 2025. Chairman and CEO Geoff Martha will deliver a presentation at 11:00 a.m. EDT, followed by a Q&A session with CFO Thierry Piéton. The event will be webcast live and archived on Medtronic's investor relations website.
Medtronic, headquartered in Galway, Ireland, is a global healthcare technology leader with 95,000+ employees across 150+ countries. The company develops technologies and therapies for 70 health conditions, including cardiac devices, surgical robotics, insulin pumps, and patient monitoring systems, serving two patients every second worldwide.
Medtronic (NYSE: MDT) has scheduled the release of its fourth quarter and full fiscal year 2025 financial results for Wednesday, May 21, 2025. The company will issue a news release at 5:45 a.m. CDT, followed by a video webcast at 7:00 a.m. CDT to discuss the results. The fiscal year 2025 ended on April 25, 2025.
The healthcare technology leader has also announced its earnings release schedule for fiscal year 2026, with quarterly results planned for August 19, 2025, November 18, 2025, February 17, 2026, and May 20, 2026. Medtronic, headquartered in Galway, Ireland, employs over 95,000 people across 150+ countries, developing technologies that treat 70 health conditions including cardiac devices, surgical robotics, and insulin pumps.
Medtronic (NYSE: MDT) announced positive clinical outcomes from two studies using their Affera™ family of technologies for atrial fibrillation treatment. The Sphere-360™ single-shot PFA catheter demonstrated 88% freedom from arrhythmia recurrence and 98% pulmonary vein isolation at one year, with no reported safety events in the optimized waveform group.
The Sphere-9™ catheter showed effectiveness for linear ablation in persistent AFib patients, based on sub-analysis from the Sphere Per-AF IDE study. The device received FDA approval in October 2024. Medtronic plans to begin U.S. pivotal trials for Sphere-360 later this year.
The company currently offers two PFA solutions: the PulseSelect™ system available in over 30 countries, and the Affera system with Sphere-9 catheter available in Europe, Australia, and New Zealand. AFib affects more than 60 million people worldwide and is a progressive disease that increases risks of heart failure, stroke, and death.