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Kj Meditech Co., Ltd.

FDA Regulatory Profile

Kj Meditech Co., Ltd. has 0 FDA recalls, 0 inspections, 13 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Mar 1, 2022

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances13Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K202046LOTA SLA Dental Implant System and LOTA HA Dental Implant SystemMar 1, 2022
K173116KJ ZIRCONIA Implant SystemJun 28, 2018
K161923J2A SLA Dental Implant SystemNov 9, 2017
K151970KJ Mini Implant SystemOct 21, 2016
K150060J2A Dental Implant System, J2C Dental Implant SystemApr 2, 2015
K140051KJ EXTERNAL IMPLANT SYSTEMOct 30, 2014
K140052J2I IMPLANT SYSTEMOct 30, 2014
K121098HERO I DENTAL IMPLANT SYSTEMJan 17, 2013
K121047HERO II DENTAL IMPLANT SYSTEM, IS DENTAL IMPLANT SYSTEMOct 4, 2012
K112787KERATORAug 8, 2012
K103810KJ SUBMERGED SYSTEMSep 14, 2011
K103019KJ MASKJun 9, 2011
K053629ANCHOR PLUS/NEO ANCHOR PLUSMay 31, 2006

FDA data resources