Medical Device Manufacturer · KR , Seoul

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

2 submissions · 2 cleared · Since 2025

Total

Cleared

Denied

Remedi, Inc. has 2 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Latest FDA clearance: Oct 2026. Active since 2025. Primary specialty: Radiology.

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

Remedi, Inc. is one of 440 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.

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

2 devices

1-2 of 2