Medical Device Manufacturer · KR , Seoul

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

1 submissions · 1 cleared · Since 2025

Total

Cleared

Denied

Remedi, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Latest FDA clearance: Jul 2025. 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.

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

1 devices

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