Latest EnsoData FDA 510(k) Clearance Enables AI-Powered Sleep Diagnosis Using Pulse Oximetry Devices

Latest EnsoData FDA 510(k) Clearance Enables AI-Powered Sleep Diagnosis Using Pulse Oximetry Devices

EnsoData, a pioneer in healthcare AI, achieved FDA 510(k) clearance for groundbreaking technology that enables AI-powered sleep diagnosis using FDA-cleared pulse oximetry (pulse ox) devices. Powered by EnsoSleep PPG scoring, widely available and wearable pulse ox technology can be deployed for a high quality, accessible, and cost-effective approach to diagnosing sleep disorders, including sleep apnea.

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EnsoSleep HSAT Scoring Certificate Holders

EnsoSleep HSAT Scoring Certification for Sleep Technologists EnsoSleep Scoring Certification provides sleep technologists with the knowledge, expertise, and confidence to proficiently review, overscore, and validate EnsoSleep artificial intelligence (AI) scored

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EnsoSleep Scoring Certification

EnsoSleep Scoring Certification provides sleep technologists with the knowledge, expertise, and confidence to proficiently review, overscore, and validate EnsoSleep artificial intelligence (AI) scored studies.

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