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First AI device to detect diabetic eye disease gets FDA greenlight

On Wednesday 11 April the US Food and Drug Administration (FDA) announced the marketing approval of the first medical device to use artificial intelligence (AI) to detect more than a mild level of diabetic retinopathy, the most common cause of vision loss among diabetic patients and the leading cause of vision impairment among the US working-age population.

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The BD MAX System can help with workflow efficiency for timely patient management; diagnostic speed and accuracy to aid in fast, appropriate treatment; and testing versatility for a wide range of patients.

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