Voluntis - FDA 510(k) Cleared Devices

Voluntis has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.

Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Anesthesiology.

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

510(k) submissions have been managed by Emergo Global Consulting as regulatory consultant.