Medical Device Manufacturer · US , Fullerton , CA

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

12 submissions · 12 cleared · Since 2011

Recent clearances: LOTA SLA Dental Implant System and LOTA HA Dental Implant System, KJ ZIRCONIA Implant System

12
Total
12
Cleared
0
Denied

Kj Meditech Co., Ltd. has 12 FDA 510(k) cleared dental devices. Based in Fullerton, US.

Last cleared in 2022. Active since 2011.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.

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

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