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After three years, most insulin was delivered automatically by the system, and those who used the recommended optimal settings experienced the greatest benefits.
Japan is now the 77th country to receive regulatory approval for the Symplicity Spyral Renal Denervation System
The upcoming U.S. launch of the small-diameter OmniaSecure defibrillation lead will introduce the first FDA-approved lead for both adults and adolescent pediatric patients
Indication demonstrates Medtronic’s commitment to innovative patient-centered solutions shaping the future of TAVR
To address the widespread prevalence of varicose veins as a serious health condition, Medtronic has launched the #KabTakKarogeIgnore campaign in India. The initiative aims to build awareness of...
Albany Medical Center performs first patient procedure in clinical trial for use of peripheral vasculature liquid embolization for active arterial hemorrhage
Data highlights Americans’ shifting preferences toward chronic condition management
Exclusive distribution agreement with FMD Co. Ltd. expands peripheral arterial disease treatment portfolio with new suite of guidewires
The company also announces plans to share new gynecologic data
for the Hugo™ RAS system and conduct a telesurgery demo at the
Society of Robotic Surgery 2025 Annual Meeting in Strasbourg, France
Medtronic advances pipeline with update on multi-organ denervation study and additional data recently presented at EuroPCR 2025
The renewed partnership builds on over 30 years of collaboration
Medtronic expands its cardiac surgical and respiratory innovation portfolio with the launch of the VitalFlow ECMO System
IRCAD North America is a first-of-its-kind education and training destination in the U.S.
Customers are being asked to remove the affected devices from use and replace with an alternate means of ventilation
Large, international registry designed to expand real-world data for Symplicity blood pressure procedure for uncontrolled hypertension
Minimally invasive laser technology now with enhanced capital system improvements, offering new user interface, workflow efficiencies, and upgrade capabilities
Regulatory review process to give patients better access to innovation through expedited development, assessment, and review of investigational Nellcor™ technology