Promos

Promos Reverse Glenosphere Eccen. DIA36/+5

Registry build 21.09.26
9manufacturers in China registered for this device type
42catalogue numbers in this listing
11510(k) clearances naming this product code
6recalls on this code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWS
Manufacturer City Province Registered as Device types
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
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

Record

Regulatory record for Promos
Listed by Smith & Nephew, Inc., United States
FDA product code KWS
Device type Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Device class Class 2
Regulation 21 CFR 888.3660
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K081016
Record published 2015-08-29
Record revised 2026-02-09 (version 8)

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
Label carries lot or batch number, expiry date
Distribution end date 2022-03-17

Catalogue Numbers

Catalogue numbers for Promos
Catalogue number Size Status
75006607 In distribution
75003720 In distribution
75003711 In distribution
75006541 In distribution
75003703 In distribution
75003698 In distribution
75042186 In distribution
75006539 In distribution
75003705 In distribution
75006533 In distribution
XT001039-1 In distribution
75003697 In distribution
75003708 In distribution
75003700 In distribution
75003701 In distribution
75003709 In distribution
75003710 In distribution
75006537 In distribution
75101982 In distribution
75006601 In distribution
XT001039-2 In distribution
75003706 In distribution
75042180 In distribution
75042182 In distribution
75010867 In distribution
75003699 In distribution
75003712 In distribution
75006555 In distribution
75003719 In distribution
75006538 In distribution
75003704 In distribution
75003715 In distribution
75003702 In distribution
75003713 In distribution
75003721 In distribution
75003707 In distribution
75006550 In distribution
75042184 In distribution
75003714 In distribution
75101980 Withdrawn
75101981 Withdrawn
75101983 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Equinoxe Exactech, Inc. 442
Reunion Stryker GmbH 321
DJO Surgical Encore Medical, L.P. 266
SMR Shoulder Limacorporate 209
Tornier Flex Shoulder System Tornier Inc. 187
Anatomical Shoulder™ Zimmer, Inc. 166
Arthrex® Arthrex, Inc. 154
Comprehensive Shoulder System Biomet Orthopedics 111
Flex Shoulder System Tornier Inc. 109
Aequalis™ PerFORM+ Tornier Inc. 108
Aequalis™ Ascend™ Flex Tornier Inc. 102
Anatomic Shoulder Prosthesis Medacta International SA 90

Showing 12 of 326. All products under Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K254084 2026-04-06
K252416 2025-10-29
K230572 2023-06-07
K220847 2023-01-03
K213827 2022-03-11
K113012 2012-01-05
K030344 2003-03-04
K012788 2002-03-15
K012378 2001-12-13
K003566 2001-02-14
K994350 2000-05-23

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Promos
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Smith & Nephew, Inc. 510(k) number 2008-11-21 Not classified Other The product was breaking during use. 159 units 2012-11-27
Smith & Nephew, Inc. 510(k) number 2008-11-21 Not classified Other The product was breaking during use. 51 units 2012-11-27

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
2010-01-14 Not classified Device Design Firm received complaints of Inclination Set Screws fracturing. 1,597 units 2012-04-10
2010-01-14 Not classified Device Design Firm received complaints of Inclination Set Screws fracturing. 366 units 2012-04-10
2010-01-14 Not classified Device Design Firm received complaints of Inclination Set Screws fracturing. 362 units 2012-04-10
2010-01-14 Not classified Device Design Firm received complaints of Inclination Set Screws fracturing. 700 units 2012-04-10

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