Attune LPS
ATTUNE KNEE SYSTEM Revision LPS Insert AOX 24mm XX-Small
Who Else Makes It
Concentrated in Jiangsu (3), Shanghai (2), Zhejiang (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| 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 |
| 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 |
Record
| Listed by | Depuy (Ireland), Ireland |
|---|---|
| FDA product code | KRO |
| Device type | Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3510 |
| Establishment | Specification developer, Repacker / relabeller, Manufacturer |
| Record published | 2020-02-25 |
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 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 1517-60-320 | In distribution | |
| 1517-60-632 | In distribution | |
| 1517-60-232 | In distribution | |
| 1517-60-624 | In distribution | |
| 1517-60-124 | In distribution | |
| 1517-60-314 | In distribution | |
| 1517-60-312 | In distribution | |
| 1517-60-212 | In distribution | |
| 1517-60-118 | In distribution | |
| 1517-60-612 | In distribution | |
| 1517-60-220 | In distribution | |
| 1517-60-218 | In distribution | |
| 1517-60-322 | In distribution | |
| 1517-60-318 | In distribution | |
| 1517-60-626 | In distribution | |
| 1517-60-120 | In distribution | |
| 1517-60-629 | In distribution | |
| 1517-60-324 | In distribution | |
| 1517-60-116 | In distribution | |
| 1517-60-214 | In distribution | |
| 1517-60-316 | In distribution | |
| 1517-60-226 | In distribution | |
| 1517-60-112 | In distribution | |
| 1517-60-122 | In distribution | |
| 1517-60-329 | In distribution | |
| 1517-60-618 | In distribution | |
| 1517-60-614 | In distribution | |
| 1517-60-216 | In distribution | |
| 1517-60-326 | In distribution | |
| 1517-60-114 | In distribution | |
| 1517-60-332 | In distribution | |
| 1517-60-229 | In distribution | |
| 1517-60-616 | In distribution | |
| 1517-60-620 | In distribution | |
| 1517-60-224 | In distribution | |
| 1517-60-222 | In distribution | |
| 1517-60-622 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Link Endo-Model EVO Knee System | Waldemar Link GmbH & Co. KG | 324 |
| Endo-Model Modular Knee Prosthesis System | Waldemar Link GmbH & Co. KG | 291 |
| LinkSymphoKnee | Waldemar Link GmbH & Co. KG | 263 |
| Evolution | Microport Orthopedics Inc. | 223 |
| Legion | Smith & Nephew, Inc. | 222 |
| OSS™ Orthopedic Salvage System | Biomet Orthopedics | 211 |
| Ustar II Knee System | United Orthopedic Corp. | 185 |
| “united” Ustar II Knee System | United Orthopedic Corp. | 162 |
| Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer | Zimmer, Inc. | 157 |
| Finn Knee System | Biomet Orthopedics | 138 |
| NexGen | Zimmer, Inc. | 119 |
| Triathlon | Howmedica Osteonics Corp | 106 |
Showing 12 of 109. All products under Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K191779 | 2019-10-08 |
Recalls Naming This Product
4 recalls name this product by its own identifiers, the UDI on its label.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Depuy Orthopaedics, Inc. | UDI-DI | 2023-02-15 | Class II | Labeling Change Control | The subject product lots are being recalled because they received a higher than specified irradiation dose. This exceeds the validated range for exposure to gamma radiation of these devices and may result in changes to the implant material | 7 units |
| Depuy Orthopaedics, Inc. | UDI-DI | 2023-02-15 | Class II | Labeling Change Control | The subject product lots are being recalled because they received a higher than specified irradiation dose. This exceeds the validated range for exposure to gamma radiation of these devices and may result in changes to the implant material | 7 units |
| Depuy Orthopaedics, Inc. | UDI-DI | 2023-02-15 | Class II | Labeling Change Control | The subject product lots are being recalled because they received a higher than specified irradiation dose. This exceeds the validated range for exposure to gamma radiation of these devices and may result in changes to the implant material | 7 units |
| Depuy Orthopaedics, Inc. | UDI-DI | 2023-02-15 | Class II | Labeling Change Control | The subject product lots are being recalled because they received a higher than specified irradiation dose. This exceeds the validated range for exposure to gamma radiation of these devices and may result in changes to the implant material | 7 units |
Recalls
11 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 |
|---|---|---|---|---|
| 2026-05-19 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 160 units |
| 2026-05-19 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 66 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
| 2026-04-03 | Class II | Under Investigation by firm | The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | 3 units |
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.