Attune LPS

ATTUNE KNEE SYSTEM Revision LPS Insert AOX 24mm XX-Small

Registry build 21.09.26
7manufacturers in China registered for this device type
37catalogue numbers in this listing
1510(k) clearance
11recalls on this code

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.

Chinese manufacturers registered for FDA product code KRO
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

Regulatory record for Attune LPS
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

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 numbers for Attune LPS
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

Other products under the same FDA 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

FDA 510(k) clearances naming this product code
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.

Recalls naming the identifiers of Attune LPS
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.

Recalls referencing this product code
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.

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