Visionary Optics, LLC is one of 16286 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Visionary Optics, LLC - FDA 510(k) Cleared Devices
Recent clearances: Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B, tisilfocon A, fluoroxyfocon A), Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B, tisilfocon A), Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B)
Visionary Optics, LLC has 3 FDA 510(k) cleared medical devices. Based in Front Royal, US.
Latest FDA clearance: Feb 2024. Active since 2017. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Visionary Optics, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Eyereg Consulting, Inc. and Andrew Vision and Device Research.