Medical Device Manufacturer · US , Raliegh , NC

Neauvia North America, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2020

Total

Cleared

Denied

Neauvia North America, Inc. has 3 FDA 510(k) cleared medical devices. Based in Raliegh, US.

Last cleared in 2023. Active since 2020. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Neauvia North America, Inc.

3 devices

1-3 of 3