Neobiotech Implant System

(Ø2.0*7.0mm)

Registry build 21.09.26
3manufacturers in China registered for this device type
8catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (1), Shanghai (1), Fujian (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DZL
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Dentalmaster (Xiamen) Medical Technology Co., Ltd. Xiamen Fujian Manufacturer 1

Record

Regulatory record for Neobiotech Implant System
Listed by Neobiotech Co., Ltd., South Korea
FDA product code DZL
Device type Screw, Fixation, Intraosseous
Device class Class 2
Regulation 21 CFR 872.4880
Establishment Manufacturer
510(k) K160991
Record published 2018-11-12
Record revised 2024-07-04 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Neobiotech Implant System
Catalogue number Size Status
CTCS30 In distribution
CTS2015 In distribution
CTS2007 In distribution
CTS2008 In distribution
CTS2013 In distribution
CTS2010 In distribution
CTS2011 In distribution
CTS2018 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OsteoMed Osteomed 1,295
Faico CMF System Faico Medical, LLC 540
Neoface Neoortho Produtos Ortopédicos S/A 181
CMF Visionare Visionare LLC 155
Universal Mandible AXS Stryker Leibinger Gmbh & Co. KG 148
Tandry CMF Plate System Microware Precision Co., Ltd. 140
Screw, Fixation, Intraosseous Synthes Gmbh 132
Level ONE CMF KLS-Martin L.P. 71
MatrixMIDFACE Synthes Gmbh 65
PlusDrive Synthes Gmbh 52
Universal 2.0 MP AXS Stryker Leibinger Gmbh & Co. KG 51
MCI – Medical Concept Innovation, Inc. MCI Medical Concept Innovation Inc. 49

Showing 12 of 92. All products under Screw, Fixation, Intraosseous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K160991 2017-01-10

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer