Medical Device Manufacturer · KR , Jeollanam-Do

Neuf, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021
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
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