Vizionfocus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VizionFocus (somofilcon A) Silicone Hydrogel Soft (hydrophilic) Contact Lens, Aurora (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lens (Tinted, Color), VizionFocus (mififilcon A) Silicone Hydrogel Soft (hydrophilic) Daily Disposable Contact Lens
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vizionfocus, Inc. Ophthalmic ✕
5 devices
Cleared
Sep 10, 2025
VizionFocus (somofilcon A) Silicone Hydrogel Soft (hydrophilic) Contact Lens
Ophthalmic
111d
Cleared
Apr 10, 2025
Aurora (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lens (Tinted, Color)
Ophthalmic
108d
Cleared
Dec 17, 2024
VizionFocus (mififilcon A) Silicone Hydrogel Soft (hydrophilic) Daily...
Ophthalmic
125d
Cleared
Dec 09, 2019
Legacy (Ocufilcon D) Performance- Tinted Soft (Hydrophilic) Daily Wear...
Ophthalmic
115d
Cleared
Oct 12, 2018
ILICON (ocufilcon D) Soft (Hydrophilic) Daily Wear Contact Lenses (Tinted,...
Ophthalmic
53d