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LiViliti Health Products receives FDA clearance for CPAP sanitizer

May 4, 2026HME News Staff

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...

CPAP Sanitizing Device, CPAP Therapy, Food & Drug Administration (FDA), Liviliti Health Products, Paptizer 360

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