About This 510(k) Submission
K242413 is an FDA 510(k) clearance for the VizionFocus (mififilcon A) Silicone Hydrogel Soft (hydrophilic) Daily Disposable Contact Lens; VizionFocus Color (mififilcon A) Silicone Hydrogel Soft (hydrophilic) Daily Disposable Contact Lens, a Lenses, Soft Contact, Daily Wear (Class II — Special Controls, product code LPL), submitted by Vizionfocus, Inc. (Miaoli County, TW). The FDA issued a Cleared decision on December 17, 2024, 125 days after receiving the submission on August 14, 2024. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.5925.