Neuf, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Neuf, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TOPA12 Portable X-ray Unit, NFLK-2501 Portable X-ray Unit
2
Total
2
Cleared
0
Denied
Neuf, Inc. has 2 FDA 510(k) cleared medical devices. Based in Jeollanam-Do, KR.
Last cleared in 2023. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Neuf, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Medmonts Co., Ltd. and CTI Co., Ltd..
FDA 510(k) Regulatory Record - Neuf, Inc.
2 devices