NEO UL Anterior Cervical Plate System

4.85mm x18mm, Neo UL FA/SD Emergency FT Bone Screw

Registry build 21.09.26
14manufacturers in China registered for this device type
58catalogue numbers in this listing
14510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWQ
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14

Showing 12 of 14. All 14 manufacturers in China registered for Appliance, Fixation, Spinal Intervertebral Body

Record

Regulatory record for NEO UL Anterior Cervical Plate System
Listed by Life Spine, United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Manufacturer
510(k) K103423
Record published 2016-06-15
Record revised 2025-11-20 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for NEO UL Anterior Cervical Plate System
Catalogue number Size Status
328-016 In distribution
145-238 In distribution
114-079 In distribution
325-014 In distribution
325-010 In distribution
145-240 In distribution
113-242 In distribution
324-018 In distribution
326-010 In distribution
324-010 In distribution
145-124 In distribution
328-012 In distribution
326-018 In distribution
322-016 In distribution
321-016 In distribution
326-016 In distribution
145-248 In distribution
327-018 In distribution
113-239 In distribution
323-012 In distribution
113-829 In distribution
322-014 In distribution
324-012 In distribution
327-014 In distribution
328-018 In distribution
326-012 In distribution
145-122 In distribution
326-014 In distribution
325-016 In distribution
323-010 In distribution
321-018 In distribution
114-041 In distribution
328-014 In distribution
145-246 In distribution
321-014 In distribution
145-128 In distribution
322-012 In distribution
2012-0005 In distribution
145-120 In distribution
328-010 In distribution
327-010 In distribution
145-244 In distribution
323-016 In distribution
145-242 In distribution
327-016 In distribution
324-016 In distribution
113-916 In distribution
325-012 In distribution
323-014 In distribution
325-018 In distribution
321-012 In distribution
321-010 In distribution
145-126 In distribution
322-010 In distribution
113-238 In distribution
324-014 In distribution
113-228 In distribution
327-012 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ReLine Nuvasive, Inc. 2,998
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,568
Creo Globus Medical, Inc. 1,765
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 1,755
Ozark Cervical Plate System VB Spine LLC 1,460
Sirion Astura Medical 1,246
Apex Spine System Spinecraft LLC 1,187
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 986
Astra Spine System Spinecraft LLC 970
Zavation Zavation 966
ACP Nuvasive, Inc. 918
Polaris™ 5.5 Spinal System Biomet Spine 877

Showing 12 of 855. All products under Appliance, Fixation, Spinal Intervertebral Body

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243369 2024-12-11
K222628 2022-11-16
K180166 2018-06-22
K172131 2017-08-28
K152282 2015-11-20
K132589 2013-10-08
K130202 2013-04-29
K103423 2011-06-01
K093200 2010-01-19
K073479 2008-01-09
K070285 2007-03-13
K062643 2006-11-16
K062831 2006-10-19
K040844 2004-07-23

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