Endo-Model Standard Knee Prosthesis System

Sparepart Kit Boxes for Endo-Model SL

Registry build 21.09.26
13manufacturers in China registered for this device type
3catalogue numbers in this listing
2510(k) clearances naming this product 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.

Chinese manufacturers registered for FDA product code JDI
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

Regulatory record for Endo-Model Standard Knee Prosthesis System
Listed by Waldemar Link GmbH & Co. KG, Germany
FDA product code JDI
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device class Class 2
Regulation 21 CFR 888.3350
Establishment Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K151008
Record published 2021-08-13
Record revised 2025-09-09 (version 2)

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
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Endo-Model Standard Knee Prosthesis System
Catalogue number Size Status
16-2013/22 In distribution
16-2013/21 In distribution
16-2011/21 In distribution

Same Product Code

Other products under the same FDA 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

FDA 510(k) clearances naming this product code
Clearance Decision date
K852705 1985-08-13
K790488 1979-03-28

Recalls Naming This Product

14 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Endo-Model Standard Knee Prosthesis System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 44 units (1 US, 43 OUS)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 3 units
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 49 units (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 31 units (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 1 unit (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 7 units (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 4 units (all OUS)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 8 units (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 7 units (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 4 units (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 2 units (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 1 unit (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2026-01-12 Class II Under Investigation by firm The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. 3 units (OUS only)
Waldemar Link GmbH & Co. KG 510(k) number 2025-11-10 Class II Process control The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component. 18 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