Aesculap

Tibia Offset Stem D11X172MM Cementless

Registry build 21.09.26
7manufacturers in China registered for this device type
7catalogue numbers in this listing

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 Aesculap
Listed by Aesculap AG, Germany
FDA product code KRO
Device type Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3510
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-09-24
Record revised 2021-04-12 (version 3)

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
Distribution end date 2021-05-07

Catalogue Numbers

Catalogue numbers for Aesculap
Catalogue number Size Status
NO481 Implant Fixation : cemented Withdrawn
NO484 Figure / Size : P4 Withdrawn
NO483 Height : 9.000 MM Withdrawn
NR491K Figure / Size : Size XL Withdrawn
NO482 Height : 8.000 MM Withdrawn
NO485 Implant Fixation : cemented Withdrawn
NO486 Diameter (mm) : 41.000 MM Withdrawn

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

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