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Neobiotech Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232528Protective CapApril 30, 2024
K232049IS-III active Short ImplantMarch 28, 2024
K210903IS Multi Unit Abutment SystemJuly 23, 2021
K190849IS-III active System_S-narrow TypeAugust 14, 2019
K181137IT-III active SystemNovember 16, 2018
K181138IS-III active SystemOctober 3, 2018
K181178S-mini active FixtureJuly 24, 2018
K173938IS-III HActive FixtureMay 24, 2018
K160991Neo GBR SystemJanuary 10, 2017
K120503CMI IMPLANT IS II ACTIVEJune 18, 2012
K113554CMI IMPLANT IS SYSTEMApril 5, 2012
K112540S-MINI IMPLANT SYSTEMFebruary 3, 2012
K111761NEO TITANIUM MESH, CTI-MEMJanuary 10, 2012
K090377SINUS QUICK EB SYSTEMAugust 28, 2009
K090825SQ IS SYSTEMJuly 16, 2009
K090527SINUS QUICK IT SYSTEMJuly 14, 2009
K042339NEOPLANT IMPLANT SYSTEMNovember 2, 2004