ABG

3 catalogue numbers from 4845-0105, listed by Howmedica Osteonics Corp, United States, under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented. 9 manufacturers in China are registered for this product code.

Registry build 21.09.26
9manufacturers in China registered for this device type
3catalogue numbers in this listing
2510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (4), Shanghai (2), Zhejiang (2). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LWJ
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for ABG
Listed by Howmedica Osteonics Corp, United States
FDA product code LWJ
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
Device class Class 2
Regulation 21 CFR 888.3360
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
Record published 2015-09-24
Record revised 2018-03-29 (version 2)

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

Catalogue Numbers

Catalogue numbers for ABG
Catalogue number Size Status
4845-0105 Taper Connection: V40™ In distribution
4845-0204 Taper Connection: V40™ In distribution
4845-0203 Side: LEFT In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Iconacy i-Hip Iconacy Orthopedic Implants, LLC 154
ZMR® Zimmer, Inc. 129
Instrument Howmedica Osteonics Corp 120
Restoration Howmedica Osteonics Corp 66
U2 Hip Stem United Orthopedic Corp. 60
Trinity Acetabular Hip System Corin Limited 58
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented Exactech, Inc. 51
Omnifit Howmedica Osteonics Corp 48
Novation Exactech, Inc. 48
Endo-Model SL Knee Prosthesis System Waldemar Link GmbH & Co. KG 46
Trident Howmedica Osteonics Corp 43
Kinectiv® Zimmer, Inc. 41

Showing 12 of 131. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K023692 2003-03-20
K993601 1999-11-16

Recalls

2 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
2023-12-01 Class II Nonconforming Material/Component Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
2023-12-01 Class II Nonconforming Material/Component Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
2009-06-18 Not classified Process control Sterilization issue: During post-sterilization inspection of the outer blister packaging of the affected lots, it was determined that the outer blister did not meet the required minimum seal width. 13 total, both products. 2012-08-27

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