Wesper Next-Generation Device Cleared for Sleep Test Data Collection

The FDA has granted 510(k) clearance to Wesper’s next-generation patch for collection of data from sleeping patients over multiple nights.

Applied to the skin using a gentle adhesive, the sleep testing device features a software app for use in ongoing management of sleep disorders.

Sleep testing is used for diagnosis and treatment of sleep disorders such as sleep apnea, “as well as reducing the risk of comorbid conditions such as heart disease or dementia,” the company said.