ProSomnus reports pilot study validation of next generation RPM device

ProSomnus announced of its pilot study for the Company’s Next Generation Remote Patient Monitoring, RPM, device for Obstructive Sleep Apnea, OSA. Data from the pilot study demonstrated that an oximeter embedded in a precision medical device can accurately, safely, and continuously monitor SpO2. “This pilot study validation represents a step toward bringing sleep medicine into the P4 medicine era. The ProSomnus RPMO2 OSA Device enables sleep medicine to be more personalized, predictive, preventative, and participatory,” commented Len Liptak, Chief Executive Officer for ProSomnus Sleep Technologies. “Although we have more work to do in terms of FDA clearances, market access and commercialization, I am very proud that team ProSomnus is in the process of bringing this potentially life changing innovation to the millions of people suffering from OSA.”