Tornier Perform® Reversed Glenoid

Peripheral Screw

Registry build 21.09.26
9manufacturers in China registered for this device type
27catalogue numbers in this listing
18510(k) clearances naming this product code
3recalls on this 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 Tornier Perform® Reversed Glenoid
Listed by Tornier Inc., United States
FDA product code PHX
Device type Shoulder Prosthesis, Reverse Configuration
Device class Class 2
Regulation 21 CFR 888.3660
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2022-04-25
Record revised 2025-04-10 (version 7)

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, manufacturing date, serial number
Sizes Outer diameter 5 to 42 mm; length 15 to 54 mm

Catalogue Numbers

Catalogue numbers for Tornier Perform® Reversed Glenoid
Catalogue number Size Status
DWJ650 Length 50 mm In distribution
DWJ530 Length 30 mm In distribution
DWJ125 Length 25 mm In distribution
DWJ318 Outer Diameter 5.0 mm In distribution
DWJ645 Length 45 mm In distribution
DWJ738 Outer Diameter 5.0 mm In distribution
DWJ230 Outer Diameter 9.5 mm In distribution
DWJ411 Outer Diameter 29 mm In distribution
DWJ630 Length 30 mm In distribution
DWJ635 Outer Diameter 9.5 mm In distribution
DWJ718 Outer Diameter 5.0 mm In distribution
DWJ540 Length 40 mm In distribution
DWJ550 Outer Diameter 6.5 mm In distribution
DWJ225 Length 25 mm In distribution
DWJ023 Outer Diameter 39 mm In distribution
DWJ034 Outer Diameter 42 mm In distribution
DWJ726 Outer Diameter 5.0 mm In distribution
DWJ346 Outer Diameter 5.0 mm In distribution
DWJ354 Outer Diameter 5.0 mm In distribution
DWJ014 Outer Diameter 42 mm In distribution
DWJ734 Outer Diameter 5.0 mm In distribution
DWJ545 Outer Diameter 6.5 mm In distribution
DWJ722 Length 22 mm In distribution
DWJ002 Length 15 mm In distribution
DWJ032 Outer Diameter 36 mm In distribution
DWJ334 Outer Diameter 5.0 mm In distribution
DWJ326 Length 26 mm In distribution

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
K252788 2026-01-08
K220914 2022-10-14
K211359 2021-11-12
K213124 2021-10-26
K183696 2019-01-30
K161742 2016-11-15
K141029 2014-06-18
K120739 2012-07-05
K112144 2012-03-13
K112615 2011-10-11
K110599 2011-06-14
K100142 2010-05-06
K081059 2008-07-17
K071948 2007-10-18
K061439 2006-07-20
K050316 2005-03-16
K041873 2004-08-25
K030941 2004-05-14

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. 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
2024-01-03 Class II Packaging process control The incorrect device is contained in the labeled package. 50
2023-09-15 Class II Process change control One lot of Tournier Perform Reversed Lateralized Baseplates were found to have been manufactured with 6mm spacers instead of 3mm spacers. This nonconformance prevents the central screw from being able to thread into the baseplate. 30 units
2019-10-18 Class II Package design/selection During shipping, it is possible for the Aequalis Ascend Flex humeral stem to become unseated or otherwise move within its internal packaging restraints. Movement within the packaging may cause the product to rub against the PETG blister sh 87869 units 2021-04-09

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