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Makes earlier and more efficient identification and treatment for ASD accessible to children everywhere.
July 18, 2023
By: Charlie Sternberg
Associate Editor
EarliTec Diagnostics Inc., a digital health company developing novel diagnostic and therapeutic products for children with autism spectrum disorder (ASD) and early childhood vulnerabilities, has announced U.S. Food and Drug Administration (FDA) 510(k) authorization of the second generation of its EarliPoint Evaluation for ASD for children ages 16-30 months old. The company also announced the commercial launch for EarliPoint, which enables EarliTec to work with providers on introducing EarliPoint Evaluation and helps deliver on the company’s mission of making earlier and more efficient identification and treatment for ASD accessible to children everywhere. “Early diagnosis can make all the difference in helping children with autism get the support they need to develop essential language and communication, social, and cognitive skills. The brains of infants and young children show remarkable neuroplasticity, forming millions of neural connections as they learn and experience new things like social interaction,” said Sarabeth Broder-Fingert M.D., M.P.H. and a member of EarliTec’s Clinical Advisory Board. “By enabling clinicians to make earlier diagnoses, EarliPoint has the potential to help families take advantage of this plasticity and tailor interventions to help their children as needed to ultimately live their best and happiest lives. EarliPoint also holds the potential to enhance equity in autism diagnosis. The current standard of care leads to substantial inequity, I am optimistic that EarliPoint’s accessible design will allow for more equitable diagnosis and treatment.”
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