Vuesonic, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vuesonic, LLC - FDA 510(k) Cleared Devices
Recent clearances: VueSonic One Contact Lens Cleaning System, VueSonic Advance 2 Contact Lens Cleaning System
1
Total
1
Cleared
0
Denied
Vuesonic, LLC has 1 FDA 510(k) cleared medical devices. Based in Miami Beach, US.
Last cleared in 2021. Active since 2021. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vuesonic, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Contract In-House Counsel and Consultants,Llc (D/B/A FDA Att as regulatory consultant.
FDA 510(k) Regulatory Record - Vuesonic, LLC
1 devices