Neauvia North America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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) Regulatory Record - Neauvia North America, Inc.
3 devices