Tag: Medtronic

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The system brings surgical planning, real-time navigation, and robotic capabilities together in a single platform designed for spine procedures

Data from a US investigational device exemption clinical study for robotic-assisted hernia repair support the system's safety and effectiveness.

Medtronic announced that it would exit the ventilator market that it characterized as increasingly unprofitable.

The system brings surgical planning, real-time navigation, and robotic capabilities together in a single platform designed for spine procedures

Oct 25, 2022

Medtronic intends to pursue a separation of the company’s combined patient monitoring and respiratory Interventions businesses.

Oct 24, 2022

Medtronic received U.S. FDA approval for expanded labeling of a cardiac lead that taps into the heart’s natural electrical system.

Oct 18, 2022

Medtronic announced a fix to a subset of its HVAD pumps that may experience a significant delay to restart, or failure to restart.

Sep 23, 2022

Medtronic is recalling certain endotracheal tubes after receiving customer complaints about obstruction of the tubes while used on patients.

Sep 22, 2022

The U.S. FDA is alerting medical device users about a cybersecurity risk for the Medtronic MiniMed 600 Series Insulin Pump System.

Sep 21, 2022

Medtronic announced its LINQ II Insertable Cardiac Monitor system received 510(k) clearance by the U.S. FDA for use in pediatric patients.

According to a stockholder rights law firm, Medtronic made a number of materially false or misleading statements about its business.