Copal® Exchange G

COPAL® exchange G hip spacer is a temporary hip spacer implant as part of two-stage septic endoprosthesis revision based on bone cement. COPAL® exchange G hip spacer contains gentamicin.…

Registry build 21.09.26

COPAL® exchange G hip spacer is a temporary hip spacer implant as part of two-stage septic endoprosthesis revision based on bone cement. COPAL® exchange G hip spacer contains gentamicin. Gentamicin reduces the risk for bacterial colonization of the device and is released into the fluid surrounding the joint. COPAL® exchange G hip spacer is intended for single-use and is supplied sterile. COPAL® exchange G hip spacer is made of fully formed polymethylmethacrylate (radiopaque PMMA with gentamicin) and contains an inner stainless steel (AISI 316L) reinforcing structure. It contains the X-ray contrast medium calcium carbonate. To improve visibility in the surgical field, it has been colored with chlorophyll-copper-complex (E141).

14manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (3), Zhejiang (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWY
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Record

Regulatory record for Copal® exchange G
Listed by Heraeus Medical LLC, United States
FDA product code KWY
Device type Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Device class Class 2
Regulation 21 CFR 888.3390
Establishment Complaint-file establishment, Manufacturer
Record published 2022-05-15
Record revised 2024-05-23 (version 4)

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
Packaging Pallet of 144, carton box of 12

Catalogue Numbers

Catalogue numbers for Copal® exchange G
Catalogue number Size Status
hip S medium In distribution
hip M medium In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Resolve Modular Revision Hip Stem United Orthopedic Corp. 196
Corin Bipolar Prosthesis Corin Limited 182
Consensus® Hip System Consensus Orthopedics, Inc. 177
Consensus Hip System Shalby Advanced Technologies, Inc. 177
Instrument Howmedica Osteonics Corp 130
Bencox Hip System Corentec Co., Ltd. 126
United Hip System, U2 Bipolar Implant United Orthopedic Corp. 123
MultiPolar® Zimmer, Inc. 100
Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented Zimmer, Inc. 96
Fitmore® Hip Stem Zimmer, Inc. 75
Arcos® Modular Revision System Biomet Orthopedics 67
Acumatch L-Series Exactech, Inc. 67

Showing 12 of 352. All products under Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K220492 2022-03-23
K191016 2019-11-01

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