Vioptix, Inc. - FDA 510(k) Cleared Devices

Vioptix, Inc. has 9 FDA 510(k) cleared medical devices. Based in Irvine, US.

Latest FDA clearance: Jun 2025. Active since 2005. Primary specialty: General & Plastic Surgery.

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