United Hip System, U-Motion II HA Cup,No-Hole

U-Motion II HA Cup, no-hole, Ø50mm

Registry build 21.09.26
15manufacturers in China registered for this device type
19catalogue 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, U-Motion II HA Cup,No-Hole
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) K172833
Record published 2015-10-24
Record revised 2018-08-06 (version 5)

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
Sizes Outer diameter 44 to 80 mm

Catalogue Numbers

Catalogue numbers for United Hip System, U-Motion II HA Cup,No-Hole
Catalogue number Size Status
1306-1250 Outer Diameter 50 mm In distribution
1306-1276 Outer Diameter 76 mm In distribution
1306-1246 Outer Diameter 46 mm In distribution
1306-1280 Outer Diameter 80 mm In distribution
1306-1248 Outer Diameter 48 mm In distribution
1306-1254 Outer Diameter 54 mm In distribution
1306-1268 Outer Diameter 68 mm In distribution
1306-1264 Outer Diameter 64 mm In distribution
1306-1270 Outer Diameter 70 mm In distribution
1306-1274 Outer Diameter 74 mm In distribution
1306-1262 Outer Diameter 62 mm In distribution
1306-1256 Outer Diameter 56 mm In distribution
1306-1272 Outer Diameter 72 mm In distribution
1306-1258 Outer Diameter 58 mm In distribution
1306-1266 Outer Diameter 66 mm In distribution
1306-1252 Outer Diameter 52 mm In distribution
1306-1244 Outer Diameter 44 mm In distribution
1306-1278 Outer Diameter 78 mm In distribution
1306-1260 Outer Diameter 60 mm 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