510(k) K222885

Pegavision (Hioxifilcon A) One-Day Soft (Hydrophilic) Contact Lenses (59% Water) by Pegavision Corporation — Product Code LPL

K222885 is an FDA 510(k) premarket notification submitted by Pegavision Corporation for the device "Pegavision (Hioxifilcon A) One-Day Soft (Hydrophilic) Contact Lenses (59% Water)". The FDA issued a decision of Substantially Equivalent on May 31, 2023. The device falls under product code LPL (Lenses, Soft Contact, Daily Wear), a Class II device regulated under 21 CFR 886.5925. Pegavision Corporation has at least 10 other 510(k) clearances on record.