FDA 510(k) Applications Submitted by NEOBIOTECH CO., LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K120503 |
02/21/2012 |
CMI IMPLANT IS II ACTIVE |
NEOBIOTECH CO., LTD. |
| K112540 |
09/01/2011 |
S-MINI IMPLANT SYSTEM |
NEOBIOTECH CO., LTD. |
| K113554 |
12/01/2011 |
CMI IMPLANT IS SYSTEM |
NEOBIOTECH CO., LTD. |
| K042339 |
08/30/2004 |
NEOPLANT IMPLANT SYSTEM |
NEOBIOTECH CO., LTD. |
| K090825 |
03/26/2009 |
SQ IS SYSTEM |
NEOBIOTECH CO., LTD. |
| K160991 |
04/08/2016 |
Neo GBR System |
NEOBIOTECH CO., LTD. |
| K090377 |
02/17/2009 |
SINUS QUICK EB SYSTEM |
NEOBIOTECH CO., LTD. |
| K090527 |
02/26/2009 |
SINUS QUICK IT SYSTEM |
NEOBIOTECH CO., LTD. |
| K111761 |
06/23/2011 |
NEO TITANIUM MESH, CTI-MEM |
NEOBIOTECH CO., LTD. |
| K173938 |
12/26/2017 |
IS-III HActive Fixture |
Neobiotech Co., Ltd. |
| K210903 |
03/26/2021 |
IS Multi Unit Abutment System |
Neobiotech Co., Ltd. |
| K190849 |
04/01/2019 |
IS-III active System_S-narrow Type |
Neobiotech Co., Ltd. |
| K181137 |
04/30/2018 |
IT-III active System |
Neobiotech Co., Ltd. |
| K181138 |
04/30/2018 |
IS-III active System |
Neobiotech Co., Ltd. |
| K181178 |
05/02/2018 |
S-mini active Fixture |
Neobiotech Co., Ltd. |
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