MINNEAPOLIS, Oct. 10, 2023 (GLOBE NEWSWIRE) -- Sleepiz, a Zurich-based medical technology company providing contactless bedside patient monitoring, today announces the FDA Class II 510(k) clearance of its Sleepiz One+ device. Sleepiz One+ is a small device placed on a bedside table that measures the macro and micro-motion in a contact-free manner to extract vital signs, which can assist with the early detection of deterioration in patients with chronic medical conditions.
The FDA clearance opens doors for seamless integration of the Sleepiz One+ device into Remote Patient Monitoring (RPM) and clinical study platforms. This integration empowers healthcare professionals with comprehensive respiration and heart rate monitoring capabilities, delivering medical data for actionable insights and informed decision-making.
While providing peace of mind for the patients, physicians can reimburse the use of the device using Current Procedural Terminology (CPT) codes for RPM to bring in additional revenue. In the world of remote patient monitoring, compliance is key, and Sleepiz One+ allows for 16 out of 30 days of measurements for CPT billing purposes. The FDA clearance now makes Sleepiz available to patients suffering from chronic respiratory diseases in the U.S. for RPM and long-term monitoring – empowering over 34 million people in the U.S.
“Sleepiz One+ shifts us from a wired, wearable world to a completely wireless, continuous standard of care,” said Dr. Soumya Dash, Sleepiz CEO. “With this FDA 510(k) clearance, Sleepiz has achieved a critical milestone in the highly regulated medical device market. This is just one more step towards creating the future of healthcare.”
With an accuracy rate of 99 percent in breathing rate and 96 percent in heart rate measurements compared to gold standard methods, Sleepiz is revolutionizing healthcare and enhancing the quality of care for patients and healthcare professionals alike.
Physicians can now prescribe the Sleepiz One+ to their patients, ushering in a new era of personalized care. This versatile device offers short- and long-term respiration and heart rate monitoring, providing enhanced insights into patients' physiological statuses. It sheds light on disease progression or remission, allowing for timely interventions and patient-centric care.
Patients can monitor vital signs from the comfort of their own homes. The contactless Sleepiz One+ device is designed for ease of installation and use, offering continuous, uninterrupted, and accurate health status checks at their bedside.
Sleepiz One+ will impact projects across various sectors within the healthcare ecosystem, including:
- Hospital at Home: Facilitating hospital-level monitoring and care in the comfort of patients' homes.
- Pharmaceuticals: Enabling accurate and compliant health data collection for clinical trials and research studies.
- Skilled Nursing Facilities: Enhancing patient care by providing continuous monitoring for vulnerable and/or elderly individuals.
- Assisted Living: Supporting the elderly with unobtrusive health monitoring to maintain their independence.
- Health/Wellness: Providing individuals with insights into their overall health and well-being.
“We are grateful to our regulatory management software partner, Essenvia, for helping us to achieve this important milestone,” continues Dr. Dash. “Essenvia's easy-to-use MedTech-centric platform, combined with their team's dedicated support, expertise, and extensive experience at every step, including the 510(k) submission process, enabled us to navigate our FDA 510(k) clearance with confidence and peace of mind.”
About Sleepiz AG
Sleepiz AG (Ltd.) is a Zürich based startup with a mission to provide patient-centric disease management through seamless integration of contactless monitoring into people’s homes. Sleepiz leverages the power of sleep insights with a device that is simply placed on the bedside table. The device operates in a non-contact fashion and measures movements originating from heart contractions and breathing patterns, as well as body motions. Sleepiz One+ has received CE class IIa medical device certification in Europe and FDA class II 510(k) clearance in the US.
While currently focusing on chronic conditions, Sleepiz aims to improve people’s lives by creating the future of healthcare. By making use of wireless millimeter wave technology, sensor fusion and artificial intelligence, in the future Sleepiz is looking to extend its capabilities to diagnose sleep disorders and predict deterioration of chronic diseases to allow faster intervention and better treatment.
Sleepiz is creating the future of healthcare.
Please visit https://sleepiz.com/ for additional information and partnership/investment opportunities.
Contact
Ellie Holt
Uproar PR
eholt@uproarpr.com
A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/55431ef9-7abf-4ac5-8ef1-cd704d29d148
