Koya Medical, a healthcare company on a mission to transform lymphatic and venous care through a comprehensive suite of innovative, people-centric platforms, received Food and Drug Administration (FDA) 510(k) clearance for its Dayspring® Lite treatment for lymphedema and venous disease. Unlike traditional compression pumps that require patients to be tethered to the wall during use, the Dayspring family of treatments enables people to enjoy movement and mobility during their active compression therapy – movement that is important to both quality of life and clinical outcomes.
Dayspring Lite is a prescription-only treatment for people who need to add basic active compression to their lymphedema regimen. It uses the same innovative Flexframe™ technology and smart, rechargeable, hand-held controller available in the Dayspring flagship product. While Dayspring Lite is non-calibrated…