Wagner SL Revision®
Wagner SL Revision® Hip Stem, uncemented, ø 17/190, taper 12/14
13manufacturers in China registered for this device type
53catalogue numbers in this listing
27510(k) clearances naming this product code
40recalls on this code
Who Else Makes It
Concentrated in Jiangsu (6), Shanghai (3), Zhejiang (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| 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 |
| 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 |
| b-ONE Medical (Beijing) Co., Ltd. | Beijing | Beijing | Contract manufacturer | 7 |
| 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 |
Showing 12 of 13. All 13 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Record
| Listed by | Zimmer, Inc., United States |
|---|---|
| FDA product code | JDI |
| Device type | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3350 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter |
| Record published | 2022-12-13 |
| Record revised | 2023-12-20 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Sizes | Outer diameter 14 to 20 mm; length 190 mm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 01.00101.920 | 20 190mm | In distribution |
| 01.00109.809 | In distribution | |
| 01.00109.035 | In distribution | |
| 01.00109.803 | In distribution | |
| 01.00109.033 | In distribution | |
| 01.00101.917 | Outer Diameter 17 mm | In distribution |
| 01.00101.917 | 17 190mm | In distribution |
| 01.00101.914 | Outer Diameter 14 mm | In distribution |
| 01.00101.915 | Length 190 mm | In distribution |
| 01.00109.119 | In distribution | |
| 01.00109.810 | In distribution | |
| 01.00109.034 | In distribution | |
| 01.00101.916 | Outer Diameter 16 mm | In distribution |
| 01.00101.914 | Length 190 mm | In distribution |
| 01.00109.808 | In distribution | |
| 01.00109.117 | In distribution | |
| 01.00101.917 | Length 190 mm | In distribution |
| 01.00101.917 | Outer Diameter 17 mm | In distribution |
| 01.00101.920 | Outer Diameter 20 mm | In distribution |
| 01.00109.122 | In distribution | |
| 01.00101.918 | 18 190mm | In distribution |
| 01.00109.805 | In distribution | |
| 01.00109.032 | In distribution | |
| 01.00101.919 | Outer Diameter 19 mm | In distribution |
| 01.00109.807 | In distribution | |
| 01.00109.114 | In distribution | |
| 01.00101.916 | Outer Diameter 16 mm | In distribution |
| 01.00101.915 | Outer Diameter 15 mm | In distribution |
| 01.00109.116 | In distribution | |
| 01.00109.123 | In distribution | |
| 01.00109.801 | In distribution | |
| 01.00109.121 | In distribution | |
| 01.00109.806 | In distribution | |
| 01.00101.915 | Length 190 mm | In distribution |
| 01.00109.120 | In distribution | |
| 01.00109.804 | In distribution | |
| 01.00109.125 | In distribution | |
| 01.00101.918 | Outer Diameter 18 mm | In distribution |
| 01.00101.920 | Outer Diameter 20 mm | In distribution |
| 75.11.00-12 | In distribution | |
| 01.00101.919 | Length 190 mm | In distribution |
| 01.00101.914 | Length 190 mm | In distribution |
| 01.00109.118 | In distribution | |
| 01.00101.920 | Length 190 mm | In distribution |
| 01.00109.115 | In distribution | |
| 01.00109.802 | In distribution | |
| 01.00101.919 | 19 190mm | In distribution |
| 01.00101.916 | Length 190 mm | In distribution |
| 01.00109.031 | In distribution | |
| 01.00101.918 | Length 190 mm | In distribution |
| 75.11.00-01 | In distribution | |
| 01.00109.124 | In distribution | |
| 01.00101.918 | Length 190 mm | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | Zimmer, Inc. | 836 |
| R3 | Smith & Nephew, Inc. | 497 |
| UniSyn Hip System | Shalby Advanced Technologies, Inc. | 247 |
| UniSyn® Hip System | Consensus Orthopedics, Inc. | 247 |
| Reflection | Smith & Nephew, Inc. | 170 |
| Instrument | Howmedica Osteonics Corp | 167 |
| Echelon | Smith & Nephew, Inc. | 159 |
| B-P Total HIP System | Endotec, Inc. | 151 |
| ZCA® | Zimmer, Inc. | 149 |
| Omnifit | Howmedica Osteonics Corp | 149 |
| Ringloc HIP System | Biomet Orthopedics | 139 |
| Profemur | Microport Orthopedics Inc. | 113 |
Showing 12 of 444. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K210842 | 2021-12-10 |
| K191449 | 2020-07-16 |
| K200823 | 2020-07-09 |
| K191735 | 2020-03-20 |
| K051516 | 2005-07-27 |
| K050105 | 2005-05-17 |
| K030153 | 2003-04-01 |
| K030265 | 2003-03-04 |
| K001733 | 2000-06-20 |
| K963109 | 1997-01-09 |
| K960278 | 1996-07-25 |
| K960658 | 1996-07-16 |
| K955473 | 1996-02-16 |
| K954744 | 1996-01-23 |
| K950312 | 1995-05-17 |
| K944792 | 1995-04-26 |
| K913649 | 1991-11-13 |
| K902436 | 1990-08-29 |
| K901364 | 1990-05-18 |
| K874229 | 1987-11-03 |
| K842906 | 1984-08-24 |
| K840643 | 1984-04-17 |
| K833912 | 1983-12-22 |
| K821893 | 1982-09-14 |
| K812182 | 1981-08-18 |
| K811293 | 1981-06-24 |
| K770908 | 1977-05-23 |
Recalls
40 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.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2024-07-02 | Class II | Under Investigation by firm | Affected product has an increased risk of postoperative perisprosthetic femoral fracture (PFF). The IFU is being updated to reflect the risk of PFF. | 5,500 (US); 242,000 (OUS) | |
| 2023-07-26 | Class II | Mixed-up of materials/components | The outer package labeling and product etch are for a Size 6, however, the implant is a Size 4, and vice versa. | 24 units | |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 2022-05-20 | |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 2022-05-20 | |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 2022-05-20 | |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
| 2020-09-24 | Class II | Device Design | Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions. | 412 units total | 2022-05-20 |
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.