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Neobiotech Co., Ltd.

17 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Protective Cap (K232528)Neobiotech Co., Ltd.2024-04-30
IS-III active Short Implant (K232049)Neobiotech Co., Ltd.2024-03-28
IS Multi Unit Abutment System (K210903)Neobiotech Co., Ltd.2021-07-23
IS-III active System_S-narrow Type (K190849)Neobiotech Co., Ltd.2019-08-14
IT-III active System (K181137)Neobiotech Co., Ltd.2018-11-16
IS-III active System (K181138)Neobiotech Co., Ltd.2018-10-03
S-mini active Fixture (K181178)Neobiotech Co., Ltd.2018-07-24
IS-III HActive Fixture (K173938)Neobiotech Co., Ltd.2018-05-24
Neo GBR System (K160991)Neobiotech Co., Ltd.2017-01-10
CMI IMPLANT IS II ACTIVE (K120503)Neobiotech Co., Ltd.2012-06-18
CMI IMPLANT IS SYSTEM (K113554)Neobiotech Co., Ltd.2012-04-05
S-MINI IMPLANT SYSTEM (K112540)Neobiotech Co., Ltd.2012-02-03
NEO TITANIUM MESH, CTI-MEM (K111761)Neobiotech Co., Ltd.2012-01-10
SINUS QUICK EB SYSTEM (K090377)Neobiotech Co., Ltd.2009-08-28
SQ IS SYSTEM (K090825)Neobiotech Co., Ltd.2009-07-16
SINUS QUICK IT SYSTEM (K090527)Neobiotech Co., Ltd.2009-07-14
NEOPLANT IMPLANT SYSTEM (K042339)Neobiotech Co., Ltd.2004-11-02

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Every clearance here is in the API, with alerts when new ones post.