M2A Magnum HIP System

15 catalogue numbers from US157860, listed by Biomet Orthopedics, United States, under Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
15catalogue numbers in this listing

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 M2A Magnum HIP System
Listed by Biomet Orthopedics, United States
FDA product code KWY
Device type Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Device class Class 2
Regulation 21 CFR 888.3390
510(k) K101336
Record published 2015-10-24
Record revised 2025-05-30 (version 7)

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 M2A Magnum HIP System
Catalogue number Size Status
US157860 60MM OUTER Ø 54MM INNER Ø In distribution
US157860 60MM OUTER Ø 54MM INNER Ø In distribution
US257844 44MM OUTER Ø 38MM INNER Ø In distribution
US257860 60MM OUTER Ø 54MM INNER Ø In distribution
US157856 56MM OUTER Ø 50MM INNER Ø In distribution
US157854 54MM OUTER Ø 48MM INNER Ø In distribution
US157848 48MM OUTER Ø 42MM INNER Ø In distribution
US257856 56MM OUTER Ø 50MM INNER Ø In distribution
US157850 50MM OUTER Ø 44MM INNER Ø In distribution
US157866 66MM OUTER Ø 60MM INNER Ø In distribution
US157854 54MM OUTER Ø 48MM INNER Ø In distribution
US257852 52MM OUTER Ø 46MM INNER Ø In distribution
US157864 64MM OUTER Ø 58MM INNER Ø In distribution
US157852 52MM OUTER Ø 46MM INNER Ø In distribution
US257850 50MM OUTER Ø 44MM INNER Ø 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

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 M2A Magnum HIP System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2013-04-26 Class II Labeling mix-ups Biomet is recalling Active Articulation E1 Hip Bearing implants. Biomet has initiated this action following an investigation which identified that outer label indicates two conflicting O.D. sizes while the inner labels indicate an incorrec 8 units 2013-08-29

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