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Tempus AI Inc., a technology company leading the adoption of AI to advance precision medicine, has announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its updated Tempus Pixel, an AI-powered cardiac imaging platform. This update allows the generation of T1 and T2 inline maps, further enhancing the device’s capabilities for cardiac MR image analysis.

GE HealthCare recently announced the launch of the Voluson Performance series, the latest addition to its women’s health ultrasound portfolio. Designed to deliver detailed imaging and simplify workflow with artificial intelligence (AI) and automation tools, the new Voluson Performance 18 and 16 offers clinicians modern, innovative technology to assist with efficient care across a wide range of applications, a press release states. 

FDA’s Center for Drug Evaluation and Research, Office of New Drugs has accepted a Letter of Intent for the qualification of Liver Stiffness Measurement by Vibration-Controlled Transient Elastography as a reasonably likely surrogate endpoint for clinical trials in adults with non-cirrhotic metabolic dysfunction-associated steatohepatitis (MASH) with moderate-to-advanced liver fibrosis (scarring).