Company confirms Hugo RAS system submission to the U.S. Food and Drug Administration ...

Medtronic confirmed that its Hugo surgical robot system has been submitted to the FDA for review, alongside the successful completion of a large clinical trial evaluating its performance | According ...

William Blair analyst Brandon Vazquez said 2025 could be the first year market leader Intuitive Surgical will face meaningful ...

The US Food and Drug Administration (FDA) has granted approval for Medtronic’s OmniaSecure defibrillation lead intended for ...

Medtronic (MDT) announced positive clinical outcomes from two studies in atrial fibrillation, AFib, patients treated with the Affera family of ...

Medtronic (MDT) announced that the Expand URO Investigational Device Exemption , IDE, clinical study, the largest such study for ...

Medtronic (NYSE: MDT) today announced positive clinical outcomes from two studies of its pulsed field ablation (PFA) ...

Medtronic (NYSE:MDT) announced today that it recently submitted its Hugo surgical robot platform to the FDA for a urologic ...

Medtronic (NYSE:MDT) confirmed on Saturday the submission of regulatory filings with the FDA to obtain marketing approval for ...

Receiving FDA clearance would allow Medtronic to pair its pumps with a glucose monitor being developed for the company by ...

Medtronic has submitted 510(k) applications to the U.S. Food and Drug Administration seeking clearance for an interoperable pump.

KIMS Sunshine Hospital, Hyderabad, has joined hands with Medtronic, a medical device manufacturer, to establish a specialised centre for renal denervation therapy. The partnership, formalised ...