Medical Device Manufacturer · KR , Seoul

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

8 submissions · 8 cleared · Since 2024

Total

Cleared

Denied

JLK, Inc. has 8 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Latest FDA clearance: Mar 2026. Active since 2024. Primary specialty: Radiology.

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

Regulatory submissions have been managed by Hogan Lovells US LLP, Third Party Review Group, LLC and Hogan Lovells.

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

8 devices

1-8 of 8

Regulatory Intelligence

Regulatory consultants 510(k) submission support ecosystem

Hogan Lovells US LLP

Third Party Review Group, LLC

Hogan Lovells

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026

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

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