Eleos™

Eleos™ Stem EXTENSION17X140MM Straight, Splined, Slotted 17X140MM

Registry build 21.09.26
21manufacturers in China registered for this device type
59catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Beijing (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JWH
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
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
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Changzhou Wastonortho Medical Appliance Co., Ltd. Changzhou Jiangsu Contract manufacturer 5

Showing 12 of 21. All 21 manufacturers in China registered for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Record

Regulatory record for Eleos™
Listed by Onkos Surgical, Inc., United States
FDA product code JWH
Device type Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3560
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K161520
Record published 2017-04-03
Record revised 2023-02-03 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Radiation Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Eleos™
Catalogue number Size Status
KTAGB410E In distribution
KTAGW315E In distribution
KSP16140E In distribution
KSC14100E In distribution
KSP18100E In distribution
KTAGB510E In distribution
KTAGB210E In distribution
KSP12140E In distribution
KTAGB310E In distribution
KTAGB105E In distribution
KSP10100E In distribution
KSP13140E In distribution
KSC01065E In distribution
KTAGB215E In distribution
KSP11100E In distribution
KTAGW215E In distribution
KTAGB205E In distribution
KSP13100E In distribution
KSP10140E In distribution
KPONTP41E In distribution
KTAGW415E In distribution
KSC01265E In distribution
KSP22100E In distribution
KSP20140E In distribution
KSP20100E In distribution
KSC01500E In distribution
KSP12100E In distribution
KSP11140E In distribution
KPONTP38E In distribution
KTAGB115E In distribution
KTAGB315E In distribution
KSP15140E In distribution
KTAGW115E In distribution
KTAGB515E In distribution
KSC10100E In distribution
KSP14140E In distribution
KSP15100E In distribution
KSC01665E In distribution
KPONTP35E In distribution
KTAGB305E In distribution
KTAGB505E In distribution
KTAGW515E In distribution
KSP17100E In distribution
KTAGB110E In distribution
KPONTP32E In distribution
KPONTP29E In distribution
KSP16100E In distribution
KSP14100E In distribution
KTAGB405E In distribution
KSC01865E In distribution
KSC18100E In distribution
KTAGB415E In distribution
KSP18140E In distribution
KSC16100E In distribution
KSC12100E In distribution
KPONTP26E In distribution
KSC01465E In distribution
KSC01530E In distribution
KSP17140E In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy® Microport Orthopedics Inc. 4,423
Exult Knee Replacement System Corentec Co., Ltd. 1,770
Freedom Maxx Orthopedics Inc. 1,693
Legion Smith & Nephew, Inc. 1,534
MyKnee Medacta International SA 1,466
Journey Smith & Nephew, Inc. 1,339
Persona® Zimmer, Inc. 1,254
DJO Surgical Encore Medical, L.P. 1,131
U2 Total Knee System United Orthopedic Corp. 1,078
CKS Plus Shalby Advanced Technologies, Inc. 1,024
Lospa Modular Knee System Corentec Co., Ltd. 1,020
Natural-Knee® Zimmer, Inc. 980

Showing 12 of 1,175. All products under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Eleos™
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Onkos Surgical, Inc. UDI-DI 2025-07-11 Class II Under Investigation by firm Unidentified substance of unknown impact was identified on devices during a retrospective evaluation. 554 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