Medical Device Manufacturer · US , Jacksonville , FL

Vistakon - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001

Total

Cleared

Denied

Vistakon has 5 FDA 510(k) cleared medical devices. Based in Jacksonville, US.

Historical record: 5 cleared submissions from 2001 to 2004. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Vistakon Filter by specialty or product code using the sidebar.

Vistakon is one of 25413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vistakon

5 devices

1-5 of 5