AVS Anchor-C Cervical Cage System

Replacement Screw Extractor Draw ROD

Registry build 21.09.26
53manufacturers in China registered for this device type
59catalogue numbers in this listing
2510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (24), Guangdong (7), Zhejiang (6). 29 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LXH
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
B.Braun Medical (Suzhou) Co,.Ltd Suzhou Jiangsu Contract manufacturer 37
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Suzhou Jinsheng Plastic Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17

Showing 12 of 53. All 53 manufacturers in China registered for Orthopedic Manual Surgical Instrument

Record

Regulatory record for AVS Anchor-C Cervical Cage System
Listed by Stryker GmbH, Switzerland
FDA product code LXH
Device type Orthopedic Manual Surgical Instrument
Device class Class 1
Regulation 21 CFR 888.4540
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2019-12-02
Record revised 2022-09-16 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date
Sizes Angle 0 to 8 °; height 6 to 12 mm; depth 12 to 14 mm; width 14 to 16 mm; length 8 to 12 mm

Catalogue Numbers

Catalogue numbers for AVS Anchor-C Cervical Cage System
Catalogue number Size Status
48328770 Angle 0.0 ° In distribution
48328694 Width 16.0 mm In distribution
48328050 In distribution
48328002 In distribution
48328724 Angle 4.0 ° In distribution
48328708 Height 10.0 mm In distribution
48328680 Width 16.0 mm In distribution
48328728 Angle 8.0 ° In distribution
48328794 Width 14.0 mm In distribution
48328790 Depth 12.0 mm In distribution
48328000 In distribution
48328780 Width 14.0 mm In distribution
48328784 Height 8.0 mm In distribution
48328704 Width 14.0 mm In distribution
48328670 Width 16.0 mm In distribution
48328760 Depth 12.0 mm In distribution
48328628 Height 12.0 mm In distribution
48328001 In distribution
48328610 Angle 0.0 ° In distribution
48328764 Height 6.0 mm In distribution
48328718 Angle 8.0 ° In distribution
48328684 Depth 14.0 mm In distribution
48328200 In distribution
48328710 Height 11.0 mm In distribution
48328624 Width 16.0 mm In distribution
48328714 Angle 4.0 ° In distribution
48328620 Width 16.0 mm In distribution
48328625AR In distribution
48328660 Height 6.0 mm In distribution
48328720 Depth 12.0 mm In distribution
48328618 Angle 8.0 ° In distribution
48328700 Angle 0.0 ° In distribution
48328604 Depth 14.0 mm In distribution
48328674 Width 16.0 mm In distribution
48328812 Length 12.0 mm In distribution
48328608 Angle 8.0 ° In distribution
48328668 Width 16.0 mm In distribution
48328910 Length 10.0 mm In distribution
48328810 Length 10.0 mm In distribution
48328912 Length 12.0 mm In distribution
48328225 In distribution
48328774 Angle 4.0 ° In distribution
48328625 In distribution
48328725 In distribution
48328688 Depth 14.0 mm In distribution
48328808 Length 8.0 mm In distribution
48328698 Depth 14.0 mm In distribution
48328788 Width 14.0 mm In distribution
48328798 Width 14.0 mm In distribution
48328768 Height 6.0 mm In distribution
48328678 Depth 14.0 mm In distribution
48328500 In distribution
48328664 Depth 14.0 mm In distribution
48328908 Length 8.0 mm In distribution
48328690 Width 16.0 mm In distribution
48328778 Angle 8.0 ° In distribution
48328614 Height 11.0 mm In distribution
48328550 In distribution
48328600 Depth 14.0 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Razek Equipamentos Razek Equipamentos Ltda 11,578
Orthopedic Manual Surgical Instrument Globus Medical, Inc. 4,784
Instrument Howmedica Osteonics Corp 4,539
Orthopedic Manual Surgical Instrument Ortho Development Corp. 4,076
Knee Instruments Medacta International SA 3,944
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 3,420
Arthrex® Arthrex, Inc. 3,106
Spine Instruments Medacta International SA 2,892
Orthopedic Manual Surgical Instrument Medtronic Sofamor Danek, Inc. 2,766
Hip Instruments Medacta International SA 1,904
Medtronic Reusable Instruments Medtronic Sofamor Danek, Inc. 1,756
ReLine Nuvasive, Inc. 1,208

Showing 12 of 9,501. All products under Orthopedic Manual Surgical Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K941605 1994-08-05
K843942 1985-04-15

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. 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
2025-03-28 Class II Device Design The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery. 1588 units
2025-03-28 Class II Device Design The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery. 6407 units
2017-11-09 Class II Environmental control Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates. 320 2019-04-16

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