FDA greenlights Lumos Labs’ digital ADHD therapeutic

0419

Lumos Labs has gained US Food and Drug Administration (FDA) clearance for LumosityRx, a prescription digital therapeutic (PDT) that aims to improve attention span in adult patients with attention deficit hyperactivity disorder (ADHD) at a time where incidence of the condition in the US is on the rise.

The post FDA greenlights Lumos Labs’ digital ADHD therapeutic appeared first on Medical Device Network.

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