FDA clears Philips AI solution that provides real-time guidance during complex minimally invasive heart valve repair
Koninklijke Philips N.V. NY Registry Shares (PHG)
US:NYSE Investor Relations:
philips.com/a-w/about/investor.html
Company Research
Source: GlobeNewswire
March 26, 2026 Philips DeviceGuide uses AI to track and visualize mitral valve repair devices [1] in real time during minimally invasive procedures, supporting treatment [2]DeviceGuide integrates with Philips Azurion image-guided therapy platform that combines imaging, real-time data and intelligent software within a unified workflow to support more consistent, efficient and confidently guided minimally invasive procedures Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for EchoNavigator R5.0 with DeviceGuide, an AI-powered software solution that assists physicians during one of interventional cardiology’s most technically demanding procedures – repairing leaking mitral valves through a minimally invasive approach. DeviceGuide was developed in close collaboration with Edwards Lifesciences, the global leader in structural heart innovation,
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News
- Assessing Philips (ENXTAM:PHIA) Valuation After Recent Share Price Weakness [Yahoo! Finance]Yahoo! Finance
- Philips launches IntraSight Plus to simplify coronary interventions and advance precision careGlobeNewswire
- Philips remains No. 1 in Medtech at European Patent Office and the largest Dutch patent applicantGlobeNewswire
- Philips convenes the Annual General Meeting of Shareholders 2026GlobeNewswire
- Philips proposes new appointment and re-appointments to its Supervisory Board and CEO re-appointmentGlobeNewswire
PHG
Earnings
- 11/4/25 - Miss
PHG
Sec Filings
- 3/30/26 - Form 6-K
- 3/30/26 - Form 6-K
- 2/19/26 - Form 20-F
- PHG's page on the SEC website