Koya Medical has obtained FDA 510(k) clearance for its Dayspring compression therapy system for treating lymphedema and various diseases that hamper lymphatic flow in the lower extremities.

The device uses a low-profile active garment made of breathable mesh, a rechargeable handheld controller that can be worn on a lanyard and a mobile app that allows for customized programming. Patients using the Dayspring system receive standard-of-care active compression therapy while they wear the device.

Koya’s Dayspring system previously received FDA 510(k) clearance for use in the upper extremities in June 2020.