Medical Device Manufacturer · KR , Seoul

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

6 submissions · 6 cleared · Since 2022

Total

Cleared

Denied

Neurophet., Inc. has 6 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Latest FDA clearance: May 2026. Active since 2022. Primary specialty: Radiology.

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

Regulatory submissions have been managed by LK Consulting Group USA, Inc. and Global Medical Standard Consulting Co., Ltd..

Neurophet., Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neurophet., Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Jun 05, 2026