Neobiotech Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neobiotech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Protective Cap, IS-III active Short Implant, IS Multi Unit Abutment System
17
Total
17
Cleared
0
Denied
Neobiotech Co., Ltd. has 17 FDA 510(k) cleared dental devices. Based in Santa Fe Springs, US.
Latest FDA clearance: Apr 2024. Active since 2004.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Withus Group, Inc. and Withus Consulting, Inc..
FDA 510(k) Regulatory Record - Neobiotech Co., Ltd.
17 devices
Cleared
Apr 30, 2024
Protective Cap
Dental
253d
Cleared
Mar 28, 2024
IS-III active Short Implant
Dental
262d
Cleared
Jul 23, 2021
IS Multi Unit Abutment System
Dental
119d
Cleared
Aug 14, 2019
IS-III active System_S-narrow Type
Dental
135d
Cleared
Nov 16, 2018
IT-III active System
Dental
200d
Cleared
Oct 03, 2018
IS-III active System
Dental
156d
Cleared
Jul 24, 2018
S-mini active Fixture
Dental
83d
Cleared
May 24, 2018
IS-III HActive Fixture
Dental
149d
Cleared
Jan 10, 2017
Neo GBR System
Dental
277d
Cleared
Jun 18, 2012
CMI IMPLANT IS II ACTIVE
Dental
118d
Cleared
Apr 05, 2012
CMI IMPLANT IS SYSTEM
Dental
126d
Cleared
Feb 03, 2012
S-MINI IMPLANT SYSTEM
Dental
155d