Medical Device Manufacturer · US , Washington , DC

Ceragem Co., Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2004

Total

Cleared

Denied

Ceragem Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Washington, US.

Latest FDA clearance: Jul 2025. Active since 2004. Primary specialty: Physical Medicine.

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

Regulatory submissions have been managed by Provision Consulting Group, Inc. and LK Consulting Group USA, Inc..

FDA 510(k) Regulatory Record - Ceragem Co., Ltd.

7 devices

1-7 of 7

Data Source

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

Last updated: Apr 27, 2026