Ant-Cer II®

40 catalogue numbers from 1777-13, listed by Zimmer Spine, Inc., United States, under Appliance, Fixation, Spinal Intervertebral Body. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
40catalogue numbers in this listing
7510(k) clearances naming this product code
1recall

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 Ant-Cer II®
Listed by Zimmer Spine, Inc., United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Record published 2016-06-22
Record revised 2025-11-20 (version 8)

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
Sizes Length 24 to 96 mm

Catalogue Numbers

Catalogue numbers for Ant-Cer II®
Catalogue number Size Status
1777-13 In distribution
1707-3059 Length 59 mm In distribution
1777-15 In distribution
1755-01 In distribution
1752-01 In distribution
1707-2044 Length 44 mm In distribution
1707-2036 Length 36 mm In distribution
1760-01 In distribution
1760-03 In distribution
1777-12 In distribution
1707-2038 Length 38 mm In distribution
1760-05 In distribution
1707-4072 Length 72 mm In distribution
1707-3071 Length 71 mm In distribution
1777-14 In distribution
1707-1030 Length 30 mm In distribution
1707-3056 Length 56 mm In distribution
1760-02 In distribution
1707-3068 Length 68 mm In distribution
1707-4076 Length 76 mm In distribution
1707-2046 Length 46 mm In distribution
1707-1024 Length 24 mm In distribution
1707-2054 Length 54 mm In distribution
1707-4084 Length 84 mm In distribution
1707-3065 Length 65 mm In distribution
1707-3062 Length 62 mm In distribution
1707-3053 Length 53 mm In distribution
1707-2040 Length 40 mm In distribution
1760-04 In distribution
1707-2050 Length 50 mm In distribution
1707-2052 Length 52 mm In distribution
1707-2048 Length 48 mm In distribution
1707-1026 Length 26 mm In distribution
1707-1028 Length 28 mm In distribution
1707-4080 Length 80 mm In distribution
1707-1032 Length 32 mm In distribution
1707-2042 Length 42 mm In distribution
1707-4088 Length 88 mm In distribution
1707-4096 Length 96 mm In distribution
1707-4092 Length 92 mm 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
K143626 2015-03-20
K141500 2014-09-23
K140611 2014-05-21
K132012 2013-08-29
K122733 2012-12-07
K111796 2011-10-27
K061353 2006-08-30

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2004-08-24 Not classified Other To date, there has been one complaint reported. During a Trinica surgical case, the surgeon was provided a standard disposable, Trinica Drill Bit (part number 07.00166.001) for use with the Trinica All Through One Drill Guide Instrumentati 82 sets 2005-11-03

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