The Transcend Plus update for EPIQ CVx and Affiniti CVx systems includes new FDA-cleared AI applications and image quality enhancements designed to improve diagnostic confidence and streamline clinical workflows.
Virtual reality is opening new pathways for technician training—bringing immersive, hands-on practice to both education and clinical operations.
Philips' Spectral CT 7500 RT, now FDA-cleared, integrates spectral CT into radiotherapy, enhancing tumor visualization and targeting.
The Transcend Plus update for EPIQ CVx and Affiniti CVx systems includes new FDA-cleared AI applications and image quality enhancements designed to improve diagnostic confidence and streamline clinical workflows.
Philips announced that it would stop selling CPAP or BiPAP sleep therapy devices and other respiratory care devices in the U.S.
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Philips has nabbed U.S. FDA clearance for its X11-4t Mini 3D TEE transducer, designed to provide highly detailed images of the heart for a wider range of patients, including pediatric and complex cases, improving cardiac care and reducing the need for invasive procedures.
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The FDA has issued a safety alert regarding Philips Respironics’ DreamStation 2 CPAP machines due to reports of safety issues, including fire, smoke, burns, and overheating, and is working with the company to address the problem and provide safety recommendations to users.
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Royal Philips has introduced interoperability between its Capsule Medical Device Information Platform and Patient Information Center iX (PIC iX), enabling hospitals to access a comprehensive patient overview and streamlining the integration of data from various medical devices into a single platform.
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Royal Philips and Masimo announce U.S. FDA clearance allowing the activation of SedLine Brain Function Monitoring, Regional Oximetry (O3), and CO₂ measurements in Philips patient monitors: IntelliVue MX750 and MX850.
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The FDA received an additional 6,000 medical device reports January 1, 2023-March 31, 2023, related to PE-PUR foam used in Philips ventilators and other devices recalled in June 2021.
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Avante Health Solutions announced a significant turning point in the right to repair, specifically concerning the right to access, service, and maintain diagnostic imaging medical equipment manufactured by Philips Medical Systems for Avante's customers who own the equipment.
