Perform™ Humeral System

74 catalogue numbers from DWR1396, listed by Tornier Inc., United States, under Shoulder Prosthesis, Reverse Configuration. 9 manufacturers in China are registered for this product code.

Registry build 21.09.26
9manufacturers in China registered for this device type
74catalogue 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 Perform™ Humeral System
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 2020-11-10
Record revised 2026-02-16 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries expiry date, manufacturing date, serial number
Sizes Outer diameter 33 to 42 mm
Distribution end date 2022-04-19

Catalogue Numbers

Catalogue numbers for Perform™ Humeral System
Catalogue number Size Status
DWR1396 Outer Diameter 39 mm Withdrawn
DWR1363 Size 1 / 2 Withdrawn
DWP3393 Thickness +3 mm Withdrawn
DWR1333 Size 1 / 2 Withdrawn
DWP1396 Size 1 / 2 Withdrawn
DWR4423 Thickness +3 mm Withdrawn
DWP3366 Thickness +6 mm Withdrawn
DWR2366 Thickness +6 mm Withdrawn
DWP4363 Thickness +3 mm Withdrawn
DWR3390 Size 1 / 2 Withdrawn
DWP2360 Outer Diameter 36 mm Withdrawn
DWR2423 Outer Diameter 42 mm Withdrawn
DWR3336 Size 1 / 2 Withdrawn
DWR3360 Thickness +0 mm Withdrawn
DWP1393 Outer Diameter 39 mm Withdrawn
DWR3363 Outer Diameter 36 mm Withdrawn
DWP3363 Outer Diameter 36 mm Withdrawn
DWP1333 Outer Diameter 33 mm Withdrawn
DWP2426 Outer Diameter 42 mm Withdrawn
DWR3393 Outer Diameter 39 mm Withdrawn
DWR3333 Outer Diameter 33 mm Withdrawn
DWP3396 Size 1 / 2 Withdrawn
DWR2390 Thickness +0 mm Withdrawn
DWR1390 Outer Diameter 39 mm Withdrawn
DWR2363 Thickness +3 mm Withdrawn
DWR4363 Size 3 / 4 Withdrawn
DWR1393 Outer Diameter 39 mm Withdrawn
DWR3396 Outer Diameter 39 mm Withdrawn
DWP1366 Outer Diameter 36 mm Withdrawn
DWX912 Size 1 / 2 Withdrawn
DWP1330 Outer Diameter 33 mm Withdrawn
DWR4390 Outer Diameter 39 mm Withdrawn
DWP4390 Thickness +0 mm Withdrawn
DWP4396 Outer Diameter 39 mm Withdrawn
DWP2366 Size 3 / 4 Withdrawn
DWP3336 Size 1 / 2 Withdrawn
DWP3360 Size 1 / 2 Withdrawn
DWP4366 Size 3 / 4 Withdrawn
DWR2393 Thickness +3 mm Withdrawn
DWX934 Size 3 / 4 Withdrawn
DWP3330 Outer Diameter 33 mm Withdrawn
DWP4423 Thickness +3 mm Withdrawn
DWR1330 Outer Diameter 33 mm Withdrawn
DWR4420 Thickness +0 mm Withdrawn
DWP2396 Outer Diameter 39 mm Withdrawn
DWP1363 Thickness +3 mm Withdrawn
DWP1390 Size 1 / 2 Withdrawn
DWP2390 Thickness +0 mm Withdrawn
DWR1336 Size 1 / 2 Withdrawn
DWR2426 Outer Diameter 42 mm Withdrawn
DWP4426 Size 3 / 4 Withdrawn
DWR4396 Size 3 / 4 Withdrawn
DWR4360 Thickness +0 mm Withdrawn
DWP2423 Outer Diameter 42 mm Withdrawn
DWP4360 Thickness +0 mm Withdrawn
DWP3390 Size 1 / 2 Withdrawn
DWP2363 Thickness +3 mm Withdrawn
DWP3333 Size 1 / 2 Withdrawn
DWP1336 Outer Diameter 33 mm Withdrawn
DWR3366 Outer Diameter 36 mm Withdrawn
DWR3330 Size 1 / 2 Withdrawn
DWP4393 Size 3 / 4 Withdrawn
DWR4426 Outer Diameter 42 mm Withdrawn
DWR2360 Size 3 / 4 Withdrawn
DWP4420 Thickness +0 mm Withdrawn
DWP1360 Outer Diameter 36 mm Withdrawn
DWR1360 Thickness +0 mm Withdrawn
DWP2393 Outer Diameter 39 mm Withdrawn
DWR1366 Thickness +6 mm Withdrawn
DWR4393 Outer Diameter 39 mm Withdrawn
DWR4366 Thickness +6 mm Withdrawn
DWR2396 Size 3 / 4 Withdrawn
DWR2420 Outer Diameter 42 mm Withdrawn
DWP2420 Thickness +0 mm 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
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