United Hip System

U-Motion II XPE Cup Liner, 20 Degrees, 36mm ID, 48mm OD

Registry build 21.09.26
15manufacturers in China registered for this device type
31catalogue numbers in this listing
11510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (8), Shanghai (3), Zhejiang (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LZO
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
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
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 15. All 15 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Record

Regulatory record for United Hip System
Listed by United Orthopedic Corp., Taiwan
FDA product code LZO
Device type Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Device class Class 2
Regulation 21 CFR 888.3353
Establishment Contract manufacturer, Manufacturer, Exporter
510(k) K221149
Record published 2023-02-02

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 United Hip System
Catalogue number Size Status
1306-3249 In distribution
1110-1406 In distribution
1406-5055 In distribution
1306-3449 In distribution
1306-3055 In distribution
1110-5001 In distribution
1110-1000 In distribution
1306-3149 In distribution
1406-3649 In distribution
1406-3055 In distribution
1110-1405 In distribution
1306-3355 In distribution
1110-3000 In distribution
1306-3255 In distribution
1306-3555 In distribution
1306-3455 In distribution
1306-3549 In distribution
1110-1407 In distribution
1110-1400 In distribution
1110-1404 In distribution
1110-5004 In distribution
1306-3155 In distribution
1406-5649 In distribution
1306-3049 In distribution
1110-5003 In distribution
1110-5007 In distribution
1110-5000 In distribution
1110-5006 In distribution
1110-5005 In distribution
1306-3349 In distribution
1110-5002 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Libertas Maxx Orthopedics Inc. 1,832
Redapt Smith & Nephew, Inc. 326
Bencox Hip System Corentec Co., Ltd. 295
M-Vizion Femoral Revision System Medacta International SA 289
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Zimmer, Inc. 280
Profemur® Microport Orthopedics Inc. 229
DJO Surgical Encore Medical, L.P. 162
Instrument Howmedica Osteonics Corp 152
Alteon Exactech, Inc. 151
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Exactech, Inc. 136
Resolve Modular Revision Hip Stem United Orthopedic Corp. 136
Wagner SL Revision® Zimmer, Inc. 133

Showing 12 of 691. All products under Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253948 2026-09-02
K243466 2025-01-06
K242249 2024-08-30
K221149 2023-01-05
K183312 2019-08-08
K170089 2017-10-06
K163441 2017-08-25
K152530 2016-03-14
K132455 2013-09-03
K122185 2013-02-22
K112463 2011-09-23

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