Medical Device Manufacturer · KR , Seoul

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

4 submissions · 4 cleared · Since 2022

Total

Cleared

Denied

Neurophet., Inc. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Latest FDA clearance: Jan 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.

FDA 510(k) cleared devices by Neurophet., Inc.

4 devices

1-4 of 4