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Hyperfine (HYPR) announces the receipt of FDA clearance for its ninth-generation AI-powered Swoop system software.
QDEL announces the FDA's clearance for its VITROS syphilis assay, which boosts the company's infectious disease testing portfolio.
ZYXI recently received the Food and Drug Administration clearance for its new TensWave device. TensWave is designed to provide a comprehensive pain...
Discover how CARDIO, an FDA-cleared AI-powered point-of-care ultrasound diagnostic software, revolutionizes cardiac care.
Discover how CARDIO, an FDA-cleared AI-powered point-of-care ultrasound diagnostic software, revolutionizes cardiac care.
SI-BONE (SIBN) receives FDA 510(k) clearance for its iFuse TORQ TNT implant system, followed by a Breakthrough Device Designation award by the FDA.