FX V135 Shoulder Prosthesis

203-0906 FX V135 Humeral CUP 135/145° Stability PE/TA6V Ø36 +6

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 FX V135 Shoulder Prosthesis
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 2024-01-23
Record revised 2025-03-06 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date, serial number
Sizes Circumference 36 mm
Distribution end date 2026-06-30

Catalogue Numbers

Catalogue numbers for FX V135 Shoulder Prosthesis
Catalogue number Size Status
206-3902 In distribution
951-5612 In distribution
206-4332 In distribution
906-0028 In distribution
951-5208 In distribution
206-5034 In distribution
206-5032 In distribution
206-4804 In distribution
206-4134 In distribution
206-4132 In distribution
951-5410 In distribution
951-0436 Circumference 36 mm In distribution
206-4832 In distribution
206-4304 In distribution
206-4604 In distribution
951-0437 In distribution
951-5614 In distribution
206-3934 In distribution
206-4104 In distribution
206-4602 In distribution
206-4802 In distribution
951-5210 In distribution
206-3932 In distribution
951-5412 In distribution
206-4632 In distribution
951-5616 In distribution
206-4834 In distribution
906-0015 In distribution
206-5004 In distribution
206-4102 In distribution
206-4302 In distribution
206-5002 In distribution
951-5414 In distribution
206-3904 In distribution
951-5212 In distribution
206-4634 In distribution
206-4334 In distribution
203-0906 Withdrawn
203-0909 Withdrawn
202-0806 Withdrawn
202-0906 Withdrawn
202-0903 Withdrawn
203-0803 Withdrawn
204-0906 Withdrawn
204-0803 Withdrawn
203-0903 Withdrawn
202-0909 Withdrawn
204-0806 Withdrawn
203-0806 Withdrawn
204-0809 Withdrawn
202-0809 Withdrawn
202-0803 Withdrawn
204-0909 Withdrawn
203-0809 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