FDA

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The U.S. Food and Drug Administration (FDA) has officially cleared AnX Robotica's NaviCam ProScan, an innovative AI-assisted reading tool designed to streamline the assessment of small bowel capsule endoscopy in adults. This significant…

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Elon Musk's brain-implant company Neuralink says the U.S. Food and Drug Administration (FDA) has given the green light to its first-in-human clinical trial. The FDA nod "represents an important first step that will one day allow our…

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The United States Food and Drug Administration has approved for emergency use a single booster dose of Pfizer/BioNTech’s COVID-19 vaccine for children ages 5 to 11. FDA said, the booster dose, should come at least five months after the…