Advanced Vision Technologies is one of 13017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Vision Technologies - FDA 510(k) Cleared Devices
Recent clearances: EYEPRINTPRO (ROFLUFOCON D) SCLERAL GP LENSES, AVT NATURASOFT
2
Total
2
Cleared
0
Denied
Advanced Vision Technologies has 2 FDA 510(k) cleared medical devices. Based in Grand Junction, US.
Historical record: 2 cleared submissions from 2012 to 2016. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Advanced Vision Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Advanced Vision Technologies
2 devices