MRS

Humeral Intercalary Stem

Registry build 21.09.26
8manufacturers in China registered for this device type
30catalogue numbers in this listing
6510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Shanghai (3), Jiangsu (3), Zhejiang (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HSD
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
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
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for MRS
Listed by Howmedica Osteonics Corp, United States
FDA product code HSD
Device type Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
Device class Class 2
Regulation 21 CFR 888.3690
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
510(k) K954559
Record published 2015-09-24
Record revised 2025-03-06 (version 4)

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
Sizes Length 25 to 115 mm

Catalogue Numbers

Catalogue numbers for MRS
Catalogue number Size Status
6487-1-140 In distribution
6487-1-040 In distribution
6487-1-120 In distribution
6487-7-115 Diameter: 11.0 Millimeter In distribution
6487-5-076 Stem Length: 75.0 Millimeter In distribution
6487-5-101 Stem Length: 100.0 Millimeter In distribution
6487-5-044 Diameter: 44.0 Millimeter In distribution
6487-5-010 In distribution
6487-6-115 Diameter: 9.0 Millimeter In distribution
6487-2-075 Diameter: 7.0 Millimeter In distribution
6487-1-060 In distribution
6487-3-075 Length 75.0 mm In distribution
6487-5-075 Diameter: 7.0 Millimeter In distribution
6487-5-115 Diameter: 7.0 Millimeter In distribution
6487-6-076 Stem Length: 75.0 Millimeter In distribution
6487-5-040 Diameter: 40.0 Millimeter In distribution
6487-4-115 Length 115.0 mm In distribution
6487-7-101 Length 75.0 mm In distribution
6487-4-075 Length 75.0 mm In distribution
6487-8-051 Stem Length: 50.0 Millimeter In distribution
6487-6-051 Stem Length: 50.0 Millimeter In distribution
6487-2-115 Length 115.0 mm In distribution
6487-3-115 Diameter: 9.0 Millimeter In distribution
6487-1-080 In distribution
6487-6-101 Stem Length: 100.0 Millimeter In distribution
6487-7-075 Diameter: 11.0 Millimeter In distribution
6487-1-100 In distribution
6487-6-075 Diameter: 9.0 Millimeter In distribution
6487-7-076 Stem Length: 75.0 Millimeter In distribution
6487-9-051 Length 50.0 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Equinoxe Exactech, Inc. 345
SMR Shoulder Limacorporate 182
FX V135 Fx Shoulder Solutions SAS 127
Acumed Acumed LLC 112
Promos Smith & Nephew, Inc. 104
Trabecular Metal® Zimmer, Inc. 90
Bigliani/Flatow® Zimmer, Inc. 86
Comprehensive® Shoulder System Biomet Orthopedics 85
Arthrex® Arthrex, Inc. 75
SMR System Limacorporate 72
DJO Surgical Encore Medical, L.P. 70
Humeris Shoulder Fx Solutions 69

Showing 12 of 241. All products under Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K070963 2007-05-04
K062845 2006-12-13
K061677 2006-07-10
K040128 2004-03-26
K032264 2003-08-08
K001419 2000-07-27

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20

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