TaperFit Cemented Hip System
TaperFit Hip Stem 45mm Offset Standard Stem size 4
5manufacturers in China registered for this device type
40catalogue numbers in this listing
Who Else Makes It
Concentrated in Jiangsu (3), Shanghai (1), Zhejiang (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Canwell Medical Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 42 |
| Suzhou Elite Precision Machinery Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 35 |
| Suzhou Ahno Medical Devices Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 17 |
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
Record
| Listed by | Corin Limited, United Kingdom |
|---|---|
| FDA product code | JDG |
| Device type | Prosthesis, Hip, Femoral Component, Cemented, Metal |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3360 |
| Establishment | Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K142761 |
| Record published | 2016-08-17 |
| Record revised | 2024-09-11 (version 7) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Radiation Sterilization |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 588.3801 | In distribution | |
| E922.232 | In distribution | |
| 588.6360 | In distribution | |
| E922.240 | In distribution | |
| 340.328 | In distribution | |
| 588.9382 | In distribution | |
| E922.432 | In distribution | |
| 588.6500 | In distribution | |
| 588.9380 | In distribution | |
| 588.3803 | In distribution | |
| 588.6454 | In distribution | |
| 588.9384 | In distribution | |
| 588.9008 | In distribution | |
| 588.9102 | In distribution | |
| 588.6453 | In distribution | |
| E922.032 | In distribution | |
| 588.3600 | In distribution | |
| E922.028 | In distribution | |
| E922.040 | In distribution | |
| 588.5001 | In distribution | |
| 588.9450 | In distribution | |
| 340.400 | In distribution | |
| 588.9012 | In distribution | |
| 279.000 | In distribution | |
| 588.9503 | In distribution | |
| E922.228 | In distribution | |
| E922.332 | In distribution | |
| E922.328 | In distribution | |
| 588.5002 | In distribution | |
| 588.6384 | In distribution | |
| 588.6450 | In distribution | |
| 588.6383 | In distribution | |
| 588.9451 | In distribution | |
| 588.6451 | In distribution | |
| 588.9103 | In distribution | |
| 588.4504 | In distribution | |
| 588.6504 | In distribution | |
| 588.9300 | In distribution | |
| 588.9453 | In distribution | |
| E922.436 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| R3 | Smith & Nephew, Inc. | 554 |
| Emperion | Smith & Nephew, Inc. | 262 |
| Reflection | Smith & Nephew, Inc. | 253 |
| Spii Model Lubinus | Waldemar Link GmbH & Co. KG | 174 |
| Polar | Smith & Nephew, Inc. | 132 |
| Anthology | Smith & Nephew, Inc. | 129 |
| Echelon | Smith & Nephew, Inc. | 122 |
| Synergy | Smith & Nephew, Inc. | 102 |
| Prosthesis, Hip, Femoral Component, Cemented, Metal | Smith & Nephew, Inc. | 93 |
| Trigen | Smith & Nephew, Inc. | 66 |
| Prosthesis Head B | Waldemar Link GmbH & Co. KG | 62 |
| Corin Taper-Fit Total Hip System | Corin Limited | 55 |
Showing 12 of 71. All products under Prosthesis, Hip, Femoral Component, Cemented, Metal
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Corin Limited | 510(k) number | 2022-07-12 | Class II | Under Investigation by firm | Some of the devices did not pass fatigue testing. | 1 | 2026-05-04 |
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.