Medtech Company Recognized Among Clarivate’s Top 100 Global Innovators
With a focus on data and AI, the company has introduced advancements in imaging, diagnostics, and image-guided therapy.
With a focus on data and AI, the company has introduced advancements in imaging, diagnostics, and image-guided therapy.
Philips has introduced a 160cm FDA-approved version of its LumiGuide navigation wire, powered by FORS technology.
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.
With a focus on data and AI, the company has introduced advancements in imaging, diagnostics, and image-guided therapy.
Royal Philips and Northwell Health have entered into a seven-year agreement to help the health system standardize patient monitoring.
Read MorePhilips Respironics recalled certain reworked ventilators for issues related to foam adhesion failure and foam debris.
Read MoreRecent medical device reports regarding Philips’ CPAP machines registered additional fatalities, expanding the number of reported deaths.
Read MoreThe FDA is providing additional information to patients, caregivers, and healthcare providers about two recent issues in certain ventilators.
Read MorePhilips has experienced thousands of complaints, lawsuits, criminal investigations, and a potential DOJ settlement related to CPAP recalls.
Read MorePhilips has received 510(k) clearance from the U.S. FDA for its newest ultrasound system, the 5000 Compact Series.
Read MorePhilips' recent recall regarding certain BiPAP machines has been classified as a Class I recall, according to the U.S. FDA.