Medical Device Manufacturer · FR , Paris

Voluntis Sa. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2016

Total

Cleared

Denied

Voluntis Sa. has 5 FDA 510(k) cleared medical devices. Based in Paris, FR.

Last cleared in 2023. Active since 2016. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Voluntis Sa.

5 devices

1-5 of 5