Vizionfocus, Inc. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
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
Vizionfocus, Inc. has 5 FDA 510(k) cleared medical devices. Based in Zhunan Township, TW.
Latest FDA clearance: Sep 2025. Active since 2018. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vizionfocus, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Eyereg Consulting, Inc. and Andre Vision and Device Research.