Medtronic Stock Price, News & Analysis

Medtronic has received CE Mark approval for a one-month dual antiplatelet therapy (DAPT) indication for high bleeding risk (HBR) patients implanted with its Resolute Onyx™ Drug-Eluting Stent. This first-of-its-kind global approval allows shorter DAPT regimens for HBR patients, which comprise nearly 40% of all PCI patients. The decision is based on the Onyx ONE Global Study, demonstrating non-inferior outcomes compared to a competitive device. Medtronic aims to secure similar approval in the U.S. after submitting relevant data to the FDA.

Medtronic plc (NYSE: MDT) will participate in the Goldman Sachs 41st Annual Global Healthcare Conference on June 9, 2020. CEO Geoff Martha will speak starting at 8:00 a.m. EDT. A live audio webcast will be accessible on Medtronic's Investor Relations site, with an archive available later the same day. Medtronic, headquartered in Dublin, is a global leader in medical technology, employing over 90,000 people and serving more than 150 countries.

Medtronic (NYSE: MDT) announced its participation in the Jefferies 2020 Global Healthcare Conference on June 3, 2020. Karen Parkhill, the CFO, will address questions at 2:30 p.m. EDT. A live audio webcast will be accessible via the Investor Events link on the Medtronic investor relations page, with a replay available later the same day. Medtronic operates globally, employing over 90,000 people and serving patients in more than 150 countries, focusing on advancing healthcare solutions.

Medtronic (NYSE: MDT) announced its participation in the Bernstein 36th Annual Strategic Decisions Conference on May 29, 2020. CEO Geoff Martha will present and address questions starting at 9:00 a.m. EDT. The event will be held virtually and can be accessed through the Investor Events link on Medtronic's investor relations page. An archive of the presentation will be available later that day. Medtronic is a leader in medical technology, operating in over 150 countries and focused on improving global healthcare.

Medtronic (NYSE: MDT) announced FDA approval for the Android version of its Guardian Connect continuous glucose monitoring (CGM) system. This system alerts users of potential high or low glucose events up to 60 minutes in advance and aims to enhance the diabetes management experience. The Guardian Connect app will introduce features such as an in-app Startup Wizard and customizable alert functions. A real-world study showed that predictive alerts helped patients avoid 65% of low glucose excursions. Updated systems are expected to ship in summer 2020.

Medtronic plc (NYSE: MDT) reported Q4 2020 revenue of $6.0 billion, down 26% reported and 25% organic, impacted by COVID-19. Q4 GAAP diluted EPS was $0.48, while non-GAAP diluted EPS stood at $0.58, reflecting a 62% decline. FY20 revenue totaled $28.913 billion, a decrease of 5.4%. Despite these challenges, Medtronic announced a quarterly dividend increase to $0.58 per share, marking its 43rd consecutive year of dividend growth. The company also reported robust cash flow from operations of $7.2 billion and free cash flow of $6.0 billion, showcasing its strong financial position.

Medtronic announces the U.S. launch of Kyphon Assist™ Directional Cannula, designed for use with balloon kyphoplasty (BKP) products to treat vertebral compression fractures. This innovative device enhances physician control during procedures and improves height restoration. The Kyphon Assist is compatible across Medtronic's BKP product portfolio, offering benefits like directional control and reduced cement leakage. Vertebral compression fractures affect 1.4 million people globally, with many at risk due to osteoporosis. Medtronic aims to expand capabilities in vertebral augmentation treatments.

Medtronic (NYSE: MDT) announced the appointment of Jeffrey J. Popma, M.D., as Vice President and Chief Medical Officer, effective June 22, 2020. Dr. Popma will lead medical initiatives in the Coronary, Renal Denervation, and Structural Heart divisions. With over 20 years in interventional cardiology, he aims to enhance cardiovascular device innovation and clinical research. His extensive experience includes directing numerous clinical trials and publishing over 500 scientific articles. Nina Goodheart and Geoff Martha expressed enthusiasm about Dr. Popma joining the executive team.

Medtronic (NYSE: MDT) presented significant clinical trial results at the 2020 SCAI Scientific Sessions. The 10-year outcomes for the Melody™ Transcatheter Pulmonary Valve (TPV) showed robust long-term safety and effectiveness, with 97% of patients experiencing minimal pulmonary regurgitation. Additionally, the investigational Harmony™ TPV trial successfully met its primary endpoints at six months, with 89% of participants achieving acceptable hemodynamic function. These results underscore Medtronic's commitment to improving therapies for congenital heart disease patients.