Vuesonic, LLC - FDA 510(k) Cleared Devices
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.
1 devices