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Forty-two of the more than 500 FDA authorizations are from GE Healthcare.
December 1, 2022
By: Michael Barbella
GE Healthcare is making significant strides in the artificial intelligence sphere, having topped a U.S. Food and Drug Administration (FDA) list of AI-enabled medical device authorizations. The company’s 42 FDA 510(k) clearances—more than any other medtech firm—reflects the successful execution of the company’s AI strategy, which is centered on addressing three key healthcare challenges: health system efficiency and access, health outcomes, and system interoperability/workflow integration. “The future of healthcare is harnessing raw data and using it to help clinicians provide better patient care. For AI to be effective, it should be seamless and within existing workflows, while uncovering patterns that complement those generated by humans,” said Vignesh Shetty, senior vice president and general manager, Edison AI and Platform, GE Healthcare. “GE Healthcare’s digital strategy is to look at AI to help clinicians achieve clinical and operational outcomes that create maximum impact for patients, providers and health systems. From big iron MRI scanners used by doctors to detect tumors on the prostate gland to mobile x-ray units in the ER or ICU that technicians use to image the lungs of COVID-19 patients at their bedside, we are seeing a tangible impact with our AI embedded on the device where and when clinicians need it. AI is an incredible lever to tackle problems at a speed and scale that our providers are coming to expect, to help save lives and improve outcomes for millions of patients everywhere.” GE Healthcare’s AI strategy includes Edison Health Services, a software technology. The software is designed to aggregate data from multiple sources and vendors to enable clinical applications that support integrated care pathway management and holistic patient views. It is designed to be vendor agnostic and can include a healthcare-specific AI toolkit for building and running applications. The FDA’s webpage, Artificial Intelligence and Machine Learning (AI/ML)-Enabled Medical Devices, provides a list of devices that have been authorized via 510(k) clearance, De Novo requests, or premarket approval (PMA). Included in the list are 42 GE Healthcare 510(k) clearances for AI-powered and data-driven solutions across the company’s product portfolio. These products are designed to help encourage greater diagnostic confidence across multiple care pathways such as oncology, cardiology, and neurology, by helping to ease the burden of care and improve workflows for healthcare systems worldwide. Examples include:
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