U2™ Hip

XPE cup liner trial, ID 36mm, 10°x54mm

Registry build 21.09.26
14manufacturers in China registered for this device type
25catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (7), 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 KWY
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
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
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Record

Regulatory record for U2™ Hip
Listed by United Orthopedic Corp., Taiwan
FDA product code KWY
Device type Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Device class Class 2
Regulation 21 CFR 888.3390
Establishment Contract manufacturer, Manufacturer, Exporter
510(k) K123550
Record published 2017-05-18
Record revised 2020-12-21 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for U2™ Hip
Catalogue number Size Status
1403-2350 ID 32mm, 0°x50mm In distribution
1201-2722-RB Ø22mm, +9mm In distribution
1403-2654 ID 36mm, 10°x54mm In distribution
1403-2144 ID 28mm, 0°x44mm In distribution
1403-2754 ID 36mm, 0°x54mm In distribution
1403-2046 ID 28mm, 10°x46mm In distribution
1403-2670 ID 36mm, 10˚x70mm In distribution
1201-2122-RB Ø22mm, +0mm In distribution
1403-2054 ID 28mm, 10°x54mm In distribution
1403-2766 ID 36mm, 0°x66mm In distribution
1403-2050 ID 28mm, 10°x50mm In distribution
1403-2266 ID 32mm, 10°x66mm In distribution
1201-2522-RB φ22mm, +6mm In distribution
1403-2060 ID 28mm, 10°x60mm In distribution
1403-2762 ID 36mm, 0°x62mm In distribution
1201-2522 φ22mm, +6mm In distribution
1403-2262 ID 32mm, 10°x62mm In distribution
1403-2256 ID 32mm, 10°x56mm In distribution
1403-2666 ID 36mm, 10°x66mm In distribution
1403-2064 ID 28mm, 10°x64mm In distribution
1403-2758 ID 36mm, 0°x58mm In distribution
1403-2770 ID 36mm, 0°x70mm In distribution
1403-2658 ID 36mm, 10°x56mm In distribution
1403-2662 ID 36mm, 10°x62mm In distribution
1403-2148 ID 28mm, 0°x48mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Resolve Modular Revision Hip Stem United Orthopedic Corp. 196
Corin Bipolar Prosthesis Corin Limited 182
Consensus® Hip System Consensus Orthopedics, Inc. 177
Consensus Hip System Shalby Advanced Technologies, Inc. 177
Instrument Howmedica Osteonics Corp 130
Bencox Hip System Corentec Co., Ltd. 126
United Hip System, U2 Bipolar Implant United Orthopedic Corp. 123
MultiPolar® Zimmer, Inc. 100
Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented Zimmer, Inc. 96
Fitmore® Hip Stem Zimmer, Inc. 75
Arcos® Modular Revision System Biomet Orthopedics 67
Acumatch L-Series Exactech, Inc. 67

Showing 12 of 352. All products under Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K152439 2016-04-07
K101670 2010-10-08
K050269 2005-08-29

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of U2™ Hip
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Orthopedic Alliance, LLC 510(k) number 2013-02-20 Class II Labeling design The recall of the Loaner Bin and Sterilization Trays for implants and instruments was initiated by Orthopedic Alliance because the directions for use and surgical techniques were not being provided to every physician
and for every surgery.
50 units 2014-03-26

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