Press Releases March 25, 2026

Philips launches IntraSight Plus to simplify coronary interventions and advance precision care

Philips launches FDA-cleared IntraSight Plus system to enhance precision and efficiency in coronary interventions

By Hana Yamamoto PHG
Philips launches IntraSight Plus to simplify coronary interventions and advance precision care
PHG

Royal Philips has launched IntraSight Plus, an integrated interventional cardiology platform cleared by the FDA and CE marked for Europe. The system combines diagnostic imaging and physiology tools on a single screen, streamlining workflow, improving precision in treatment planning, and potentially reducing operation times by up to 47%. The launch aims to support minimally invasive coronary procedures, helping clinicians make more confident decisions and improve patient outcomes.

Key Points

  • IntraSight Plus integrates intravascular ultrasound (IVUS) and physiology tools like iFR/FFR with angiography to provide comprehensive coronary intervention guidance.
  • The platform is designed to significantly improve workflow efficiency, offering up to 47% system operation time savings in both the US and Europe, enabling bedside procedural control without disrupting sterile fields.
  • The system supports precise treatment planning and stent placement through tri-registration technology, potentially enhancing outcomes for complex percutaneous coronary interventions (PCI).
  • The launch influences the healthcare technology sector, specifically impacting cardiovascular medical devices, interventional cardiology, and hospital procedure efficiencies.

March 25, 2026

  • Intuitive interventional cardiology platform combines the most comprehensive set of diagnostic and treatment planning tools to help support confident decisions and improved patient care
  • With FDA clearance and CE marking, IntraSight Plus streamlines the workflow efficiency of minimally invasive coronary procedures and can enable system operation time savings up to 47% in both the USA and Europe

Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, has announced the launch of its intuitive interventional guidance platform, IntraSight Plus, which is cleared for clinical use in the USA and Europe. With CE marking and FDA 510(k) clearance, the redesigned platform combines the most comprehensive diagnostic and treatment planning tools to deliver efficiency, simplicity and precision in a single intuitive system [1]. By streamlining access to key interventional tools, IntraSight Plus enables clinicians to diagnosis, virtually plan treatment, guide device placement and verify results all on a single screen – supporting confident decision-making and improved patient outcomes.

Interventional cardiologists have traditionally relied on angiography alone for percutaneous coronary interventions (PCI), a common minimally invasive procedure. While guidelines support the use of intravascular ultrasound and physiology for PCI, systems and inputs are often separate, making adoption seem more challenging and less efficient in busy cath labs. IntraSight Plus aims to help with these challenges, bringing everything to the table through a single intuitive system that can help deliver 47% system operation time savings and enable complete control at the bedside [2].

“As more advanced technology is integrated into the cath lab, the need for connectivity between the imaging tools is more important than ever before,” said Stacy Beske, Business Leader Image Guided Therapy Devices at Philips. “IntraSight Plus was built using feedback from our customers and represents a fundamental shift in interventional cardiology – a future driven by integrated intelligence that lets physicians focus on the decision-making that only they can do.”

Innovation that simplifies complex interventions
On Thursday, March 19, 2026, Prof. Dr. Jan-Malte Sinning performed the first patient case using IntraSight Plus at Cellitinnen-Krankenhaus St. Vinzenz in Köln, Germany. The hospital recently renewed its catheterization lab infrastructure with Philips’ Azurion interventional suites. The addition of IntraSight Plus as part of this ecosystem allows for enhanced physician workflow.   

“Modern PCI is becoming increasingly complex,” said Prof. Dr. Sinning. “Intravascular imaging combined with physiology provides the level of detail we need for contemporary PCI. What stands out with IntraSight Plus is that the platform is clearly designed around how we actually work in the cath lab – combining physiology, imaging and decision-making support in a way that fits naturally into the clinical workflow.”

The patient treated in this first case presented with an acute ST-elevation myocardial infarction (STEMI) of the left anterior descending (LAD) artery two days ago and underlying complex three-vessel disease. Using the Philips Azurion interventional platform in combination with the new IntraSight Plus system, Prof. Dr. Sinning performed a complete revascularization prior to discharge.

The integrated tri-registration of angiography, physiological assessment, and intravascular imaging enabled a streamlined and intuitive workflow, allowing treatment to be focused on hemodynamically relevant lesions and ensuring optimal stent deployment to improve patient outcomes.

Delivering precision through integration

A fully redesigned system that merges Philips IntraSight and SyncVision technologies, IntraSight Plus brings Class IA IVUS and instantaneous wave-free ratio/fractional flow reserve (iFR/FFR) physiology, co-registration, tri-registration and real-time device visualization together in one system.

It enables:

  • Greater Precision: Class IA IVUS and iFR tri-registered onto one screen so clinicians can see the plaque morphology and its ischemic impact at every point along the vessel. Physicians can plan their PCI, estimate results, size and place stents and perform precise PCIs for better patient care.
  • Efficiency: Enter patient data once. Streamlined communication between IntraSight Plus and Azurion DataHandler is designed for customers to spend less time operating multiple technologies.[3]
  • Customer Control: The intuitive platform brings procedural guidance and unified control to the bedside, providing complete bedside procedural control without leaving the sterile field.

Philips’ portfolio of image-guided therapy solutions uniquely integrates best in class imaging systems and software, with specialized diagnostic and therapeutic devices to support exceptional treatment for even the most complex procedures. Built using a common Philips architecture, IntraSight Plus also connects with the company’s Azurion platform and PACS system for tighter integration within a Philips lab environment.

Availability
IntraSight Plus is FDA 510(k) cleared in the USA and CE marked in Europe. Commercial availability is subject to market release and applicable regulatory requirements.

[1] REF-00942-v1 IntraSight Plus The Most Comprehensive Claim Support
[2] IntraSight Plus Simulated Use Report, D002094363. Data on file at Philips. When compared to IntraSight, SyncVision console and Azurion. Tested in a simulated use study with Philips employees.

For further information, please contact:

Joost Maltha
Philips Global External Relations
Tel.: +31 6 1055816
E-mail: joost.maltha@philips.com

About Royal Philips 

Royal Philips (NYSE: PHG, AEX: PHIA) is a leading health technology company focused on improving people’s health and well-being through meaningful innovation. Philips’ patient- and people-centric innovation leverages advanced technology and deep clinical and consumer insights to deliver personal health solutions for consumers and professional health solutions for healthcare providers and their patients in the hospital and the home.

Headquartered in the Netherlands, the company is a leader in diagnostic imaging, ultrasound, image-guided therapy, monitoring and enterprise informatics, as well as in personal health. Philips generated 2025 sales of EUR 18 billion and employs approximately 64,800 employees with sales and services in more than 100 countries. News about Philips can be found at www.philips.com/newscenter.

Attachments

  • Philips IntraSight Plus
  • Philips IntraSight Plus screen
  • Team Germany IntraSight

Risks

  • Commercial availability is subject to regulatory approvals and market release timing, which may delay adoption and revenue realization.
  • Clinical adoption depends on physician training and acceptance; resistance to new integrated systems in cath labs could limit uptake.
  • Potential competition from other medical device companies with alternative interventional cardiology platforms could affect market share growth.

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