KTBS 3

ManaMed® Secures FDA 510(k) Clearance for PlasmaFlow® X -- a Breakthrough, Compact Sequential Compression System with All-Day Battery

Over 30% smaller footprint, double the battery life, modern USB – C charging, and an expanded LCD interface set a new bar for ...
Business Wire

AIROS Medical Receives FDA Clearance to Market New Peristaltic Pneumatic Compression Device, Truncal Garments for Lymphedema Treatment

AUDUBON, Pa.--(BUSINESS WIRE)--AIROS® Medical, Inc., a medical technology manufacturer and designer specializing in compression therapy devices that treat lymphedema and venous complications, today ...
WGHP

ManaMed® Secures FDA 510(k) Clearance for PlasmaFlow® X -- a Breakthrough, Compact Sequential Compression System with All-Day Battery

Over 30% smaller footprint, double the battery life, modern USB – C charging, and an expanded LCD interface set a new bar for performance and portability in SCDs. DENTON, Texas, Oct. 20, 2025 ...