LiViliti Health Products receives FDA clearance for CPAP sanitizer

By HME News Staff
Updated 9:45 AM CDT, Mon May 4, 2026
SARASOTA, Fla. – LiViliti Health Products has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Paptizer 360. Classified as a Class II Respiratory Accessory Microbial Reduction Device, the Paptizer 360 provides a supplemental, at-home bacterial reduction process on compatible CPAP equipment. "This clearance marks a significant milestone for LiViliti as we continue to provide users with scientifically validated tools for their respiratory health," said Brian Sharpe, CEO of LiViliti Health Products. "The Paptizer 360 offers a fast, effective, and ozone-free way to supplement daily cleaning routines." LiViliti Health Products received an equity investment from Trace Medical last year. The two companies said they would coordinate a go-to-market initiative beginning in early 2026. LiViliti Health Products specializes in accessories and maintenance solutions for CPAP users.
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