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Innobiosurg Co., Ltd.

FDA Regulatory Profile

Innobiosurg Co., Ltd. has 0 FDA recalls, 0 inspections, 15 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Dec 20, 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) clearances15Oct 4, 2026Not statedCurrent
Inspections0Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K220517IBS SystemDec 20, 2022
K220079Magicore Narrow SystemDec 14, 2022
K212517Magicore SystemOct 15, 2021
K203344Premilled Titanium Block SystemAug 25, 2021
K202418Magic UCLA Abutment SystemDec 3, 2020
K202479IBS Implant SystemSep 23, 2020
K201981Magicore SystemAug 27, 2020
K201621Magicore II SystemJul 15, 2020
K200753IBS Implant System IIJun 9, 2020
K192197Magicore II SystemApr 28, 2020
K173120CCM Abutment SystemMar 16, 2018
K162099IBS Implant System IIFeb 15, 2017
K153350IBS Implant SystemMay 9, 2016
K152520Magicore SystemJan 25, 2016
K140806IBS IMPLANT SYSTEMMar 23, 2015

FDA data resources