Orthopedic Manual Surgical Instrument

Stability Trial CUP 135-145° FOR Implant Ø32 +18 Standard Trial Humeral CUP 135/145° Ø32 +15

Registry build 21.09.26
9manufacturers in China registered for this device type
54catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (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 PHX
Manufacturer City Province Registered as Device types
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
Stryker Trauson (Changzhou) Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 3
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
Changzhou Atomic HI-Tech Radiation Co., Ltd. Changzhou Jiangsu Contract manufacturer 8

Record

Regulatory record for Orthopedic Manual Surgical Instrument
Listed by Fx Solutions, France
FDA product code PHX
Device type Shoulder Prosthesis, Reverse Configuration
Device class Class 2
Regulation 21 CFR 888.3660
510(k) K213117
Record published 2026-06-25
Record revised 2026-06-29 (version 4)

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
Storage Special storage condition: Store away from light and sunlight Store away from moisture
Distribution end date 2026-06-29

Catalogue Numbers

Catalogue numbers for Orthopedic Manual Surgical Instrument
Catalogue number Size Status
951-0120 In distribution
912-0906 In distribution
903-0055 In distribution
951-0047 In distribution
906-4016-CM1 In distribution
906-0063 In distribution
901-1009 In distribution
951-0116 In distribution
951-0114 In distribution
951-0112 In distribution
901-1006 In distribution
961-0017 In distribution
951-0118 In distribution
951-0110 In distribution
901-1003 In distribution
912-0903 In distribution
906-0023 In distribution
903-0077 In distribution
912-0909 In distribution
951-8909 Withdrawn
951-9815 Withdrawn
951-7812 Withdrawn
951-7815 Withdrawn
951-8815 Withdrawn
951-8915 Withdrawn
951-9915 Withdrawn
951-9818 Withdrawn
951-8806 Withdrawn
951-9812 Withdrawn
951-8818 Withdrawn
951-7803 Withdrawn
951-7918 Withdrawn
951-9803 Withdrawn
951-8918 Withdrawn
951-9906 Withdrawn
951-8809 Withdrawn
951-7906 Withdrawn
951-9909 Withdrawn
951-8912 Withdrawn
951-8803 Withdrawn
951-8812 Withdrawn
951-9912 Withdrawn
951-7912 Withdrawn
951-8906 Withdrawn
951-7809 Withdrawn
951-9918 Withdrawn
951-7818 Withdrawn
951-7903 Withdrawn
951-7909 Withdrawn
951-7806 Withdrawn
951-9806 Withdrawn
951-9903 Withdrawn
951-7915 Withdrawn
951-9809 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arthrex® Arthrex, Inc. 297
FX V135 Fx Shoulder Solutions SAS 131
Prima TT Glenoid Limacorporate 129
Shoulder Innovations Inset Reverse Total Shoulder Shoulder Innovations, Inc 124
Equinoxe Exactech, Inc. 123
Veritas rTSA restor3d, inc. 112
DJO Surgical Encore Medical, L.P. 109
R1 Reverse Shoulder System Catalyst Orthoscience Inc 100
Tornier Perform™ Humeral System Tornier Inc. 96
MSS – Monobloc stem Medacta International SA 92
SMR Shoulder Limacorporate 90
Humelock II Cemented Reversible Shoulder Fx Solutions 83

Showing 12 of 232. All products under Shoulder Prosthesis, Reverse Configuration

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K163669 2017-05-17
K162455 2017-01-17
K150488 2015-11-13

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