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 (MDT) is a global leader in medical technology, developing innovative healthcare solutions that address chronic diseases and complex conditions. This dedicated news hub provides investors and professionals with timely updates on the company's strategic initiatives, regulatory milestones, and technological breakthroughs.
Access authoritative information spanning earnings announcements, product approvals, partnership developments, and clinical trial outcomes. Our curated collection ensures you stay informed about MDT's advancements in cardiac care, neuromodulation, diabetes management, and surgical robotics.
Discover press releases detailing regulatory submissions, executive appointments, and global market expansions. Each update is verified for accuracy, offering insights into how Medtronic maintains its position at the forefront of medical innovation while navigating evolving healthcare landscapes.
Bookmark this page for direct access to primary source materials and analysis-free reporting on MDT's operational developments. Regular updates ensure you never miss critical information impacting the medical technology sector.
Medtronic has received the CE Mark for its SenSight™ directional lead system, enhancing Deep Brain Stimulation (DBS) therapy for movement disorders and epilepsy. This innovative system incorporates built-in sensing capabilities and works with Medtronic's Percept™ PC neurostimulator to enhance patient-specific therapy. Initial implantations took place in March 2021, with a full European launch anticipated soon. Medtronic has a long-standing commitment to advancing DBS technology, having implanted over 175,000 devices globally since 1987.
Medtronic plc (NYSE: MDT) announced the FDA's approval of revised commercial labeling for its Intellis™ Platform, showcasing the efficacy of Differential Target Multiplexed (DTM™) programming in treating chronic back pain. A randomized control trial revealed that 80% of patients using DTM SCS experienced over 50% back pain relief after three months, compared to 51% with conventional SCS. At twelve months, 84% reported significant pain relief with DTM SCS. This update strengthens Medtronic's credibility in pain management solutions.
Medtronic plc (NYSE: MDT) announced a cash dividend of $0.58 per ordinary share for Q4 FY 2021, a 7.4% increase from the previous year, reflecting its commitment to returning value to shareholders. This dividend is payable on April 16, 2021, to shareholders on record by March 26, 2021. Medtronic continues to be a part of the S&P 500 Dividend Aristocrats index, having increased its annual dividends for 43 consecutive years. The announcement aligns with prior communications made in May 2020.
Medtronic plc (NYSE: MDT) has commenced its pivotal trial for the PulseSelect™ Pulsed Field Ablation (PFA) System, aimed at treating atrial fibrillation (AF). The trial, known as PULSED AF, is the first global study with investigational device exemption approval, assessing safety and efficacy across up to 500 patients in the U.S., Canada, Europe, and Australia. PulseSelect employs a non-thermal approach to disrupt irregular heart rhythms, potentially reducing damage to surrounding tissues. Preliminary results from pilot studies showed promising efficacy with no procedural complications.
Medtronic plc (NYSE:MDT) has released new findings from the REVERSE trial, demonstrating the long-term benefits of cardiac resynchronization therapy (CRT) for patients with mild heart failure. The study indicates that patients who stabilize with CRT have similar longevity to those who improve, with five-year mortality rates at 10% for improved/stabilized patients versus 21% for worsened cases. The trial involved 406 patients, revealing a 73% lower risk of dying for CRT patients who stabilized compared to those whose condition worsened. The results emphasize the need for redefining CRT response classifications.
Medtronic plc (NYSE:MDT) reported Q3 fiscal 2021 results, showing revenue of $7.775 billion, a 0.8% increase as reported but a 1.0% decline organically. GAAP diluted EPS was $0.94, while non-GAAP diluted EPS fell 10% to $1.29. U.S. revenue decreased 2%, while non-U.S. developed markets increased 6% as reported. The Cardiac and Vascular Group saw a 4.0% decrease in revenue, and the Minimally Invasive Therapies Group experienced a 6.3% increase, partly due to COVID-19 related products. The firm refrained from providing formal financial guidance due to ongoing uncertainties.
Medtronic (NYSE:MDT) announced FDA approval for expanded MRI labeling of its InterStim™ II and InterStim™ Micro sacral neuromodulation systems using SureScan™ MRI leads. This updated labeling enhances MRI scan parameters and reduces wait times, improving patient access. New features include increased B1+rms settings for MRI scans and reduced maximum duration scan wait times from 60 to 5 minutes. The SureScan technology eliminates impedance checks before MRI, streamlining patient care. Medtronic continues to innovate in SNM therapy, highlighting over 70 FDA approvals for its InterStim portfolio.
Medtronic plc (NYSE: MDT) announced its participation in several upcoming virtual investor conferences. Key details include:
- SVB Leerink Global Healthcare Conference on February 24, 2021, at 9:20 AM EST, featuring Mike Weinstein.
- Citi's Healthcare Services Conference on February 25, 2021, at 2:25 PM EST, with Brett Wall speaking.
- Cowen Annual Healthcare Conference on March 2, 2021, at 12:50 PM EST, featuring Karen Parkhill.
- Oppenheimer Healthcare Conference on March 16, 2021, at 1:10 PM EDT, with Sean Salmon.
Webcasts will be available on Medtronic's investor relations page.
On February 17, 2021, Medtronic plc (NYSE:MDT) announced a global recall of its Valiant Navion thoracic stent graft system due to safety concerns. This decision followed reports of stent fractures and associated serious complications in patients from the Valiant Evo Global Clinical Trial. Notably, one patient death was reported, and seven out of 87 patients showed stent ring enlargement. Medtronic is conducting a thorough investigation and has urged physicians to cease use of the device while prioritizing patient safety.
Medtronic plc (NYSE:MDT) will report its third quarter financial results for fiscal year 2021 on February 23, 2021, at 5:45 a.m. CST. The report will include financial data for the quarter ending January 29, 2021. Medtronic will hold a video webcast to discuss these results at 7:00 a.m. CST, available on their investor relations website. Future earnings releases are also scheduled through fiscal year 2022.
