Revision Knee System

Femoral Augment, Posterior, Cemented, 1, 5mm

Registry build 21.09.26
21manufacturers in China registered for this device type
80catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Beijing (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JWH
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
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
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Changzhou Wastonortho Medical Appliance Co., Ltd. Changzhou Jiangsu Contract manufacturer 5

Showing 12 of 21. All 21 manufacturers in China registered for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Record

Regulatory record for Revision Knee System
Listed by Shalby Advanced Technologies, Inc., United States
FDA product code JWH
Device type Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3560
Establishment Contract manufacturer, Contract steriliser, Manufacturer
Record published 2022-01-22

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Revision Knee System
Catalogue number Size Status
2440-0-0501 In distribution
2461-0-1520 In distribution
2461-0-0814 In distribution
2420-0-0001 In distribution
2461-0-1518 In distribution
2440-0-1056 In distribution
2461-0-1110 In distribution
2431-0-0002 In distribution
2411-0-0004 In distribution
2471-0-0003 In distribution
2431-0-0005 In distribution
2440-0-0545 In distribution
2440-0-1006 In distribution
2420-0-0056 In distribution
2471-0-0001 In distribution
2420-0-0002 In distribution
2472-0-0000 In distribution
2431-0-0003 In distribution
2421-0-0001 In distribution
2420-0-0034 In distribution
2432-0-0002 In distribution
2421-0-0004 In distribution
2461-0-0818 In distribution
2432-0-0004 In distribution
2440-0-1023 In distribution
2412-0-0002 In distribution
2461-0-1510 In distribution
2431-0-0006 In distribution
2421-0-0005 In distribution
2412-0-0003 In distribution
2440-0-0512 In distribution
2440-0-1012 In distribution
2440-0-0534 In distribution
2440-0-1000 In distribution
2432-0-0006 In distribution
2421-0-0006 In distribution
2412-0-0006 In distribution
2461-0-0812 In distribution
2440-0-1034 In distribution
2461-0-1522 In distribution
2432-0-0000 In distribution
2411-0-0002 In distribution
2461-0-1516 In distribution
2461-0-0822 In distribution
2431-0-0001 In distribution
2440-0-0556 In distribution
2431-0-0004 In distribution
2461-0-1122 In distribution
2461-0-1116 In distribution
2411-0-0001 In distribution
2470-0-0002 In distribution
2461-0-1120 In distribution
2412-0-0004 In distribution
2461-0-1514 In distribution
2461-0-0816 In distribution
2440-0-0523 In distribution
2470-0-0001 In distribution
2471-0-0002 In distribution
2461-0-1114 In distribution
2412-0-0001 In distribution
2412-0-0005 In distribution
2461-0-0810 In distribution
2440-0-1001 In distribution
2421-0-0003 In distribution
2421-0-0002 In distribution
2432-0-0005 In distribution
2440-0-0500 In distribution
2461-0-1112 In distribution
2461-0-0820 In distribution
2432-0-0001 In distribution
2411-0-0005 In distribution
2470-0-0000 In distribution
2411-0-0003 In distribution
2461-0-1512 In distribution
2431-0-0000 In distribution
2461-0-1118 In distribution
2411-0-0006 In distribution
2432-0-0003 In distribution
2440-0-0506 In distribution
2440-0-1045 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy® Microport Orthopedics Inc. 4,423
Exult Knee Replacement System Corentec Co., Ltd. 1,770
Freedom Maxx Orthopedics Inc. 1,693
Legion Smith & Nephew, Inc. 1,534
MyKnee Medacta International SA 1,466
Journey Smith & Nephew, Inc. 1,339
Persona® Zimmer, Inc. 1,254
DJO Surgical Encore Medical, L.P. 1,131
U2 Total Knee System United Orthopedic Corp. 1,078
CKS Plus Shalby Advanced Technologies, Inc. 1,024
Lospa Modular Knee System Corentec Co., Ltd. 1,020
Natural-Knee® Zimmer, Inc. 980

Showing 12 of 1,175. All products under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K241180 2025-01-14

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