Aequalis™ PerFORM+

108 catalogue numbers from DWE321, listed by Tornier Inc., United States, under Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented. 9 manufacturers in China are registered for this product code.

Registry build 21.09.26
9manufacturers in China registered for this device type
108catalogue numbers in this listing
24510(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 Aequalis™ PerFORM+
Listed by Tornier 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, Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K111902
Record published 2015-10-16
Record revised 2026-02-11 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries expiry date, serial number
Sizes Angle 15 to 35 °
Distribution end date 2022-04-13

Catalogue Numbers

Catalogue numbers for Aequalis™ PerFORM+
Catalogue number Size Status
DWE321 In distribution
DWE323 In distribution
DWE413 In distribution
DWK506RA25 Size X-LARGE Withdrawn
DWK503LA15 Angle 15 ° Withdrawn
DWK406RA35 Angle 35 ° Withdrawn
DWK404LA15 Size MEDIUM Withdrawn
DWK406RA15 Angle 15 ° Withdrawn
DWK405LA35 Size LARGE Withdrawn
DWE301 Withdrawn
DWK404RA25 Angle 25 ° Withdrawn
DWK504RA35 Angle 35 ° Withdrawn
DWK403RA15 Angle 15 ° Withdrawn
DWK403LA35 Angle 35 ° Withdrawn
DWK504LA25 Angle 25 ° Withdrawn
DWE523 Withdrawn
DWK406LA35S Angle 35 ° Withdrawn
DWE411 Withdrawn
DWE433 Withdrawn
DWK504LA35 Angle 35 ° Withdrawn
DWK404RA15 Size MEDIUM Withdrawn
DWK505RA25 Size LARGE Withdrawn
DWK406RA35S Size X-LARGE Withdrawn
DWK405RA15 Angle 15 ° Withdrawn
DWK505LA35 Size LARGE Withdrawn
DWE431 Withdrawn
DWE423 Withdrawn
DWE511 Withdrawn
DWE403 Withdrawn
DWE432 Withdrawn
DWE302 Withdrawn
DWK503RA15 Size SMALL Withdrawn
DWE521 Withdrawn
DWK403LA25 Size SMALL Withdrawn
DWK506RA15 Size X-LARGE Withdrawn
DWK405RA35 Angle 35 ° Withdrawn
DWE401 Withdrawn
DWK405RA25 Size LARGE Withdrawn
DWK404RA15S Size MEDIUM Withdrawn
DWE333 Withdrawn
DWK504LA15 Size MEDIUM Withdrawn
DWK504RA15 Angle 15 ° Withdrawn
DWE332 Withdrawn
DWK403LA15 Angle 15 ° Withdrawn
DWK405RA35S Angle 35 ° Withdrawn
DWK405LA35S Size LARGE Withdrawn
DWE311 Withdrawn
DWK506LA15 Angle 15 ° Withdrawn
DWK405RA15S Size LARGE Withdrawn
DWK404RA35 Angle 35 ° Withdrawn
DWE331 Withdrawn
DWK503RA25 Size SMALL Withdrawn
DWK403LA35S Angle 35 ° Withdrawn
DWE402 Withdrawn
DWE422 Withdrawn
DWK403LA15S Angle 15 ° Withdrawn
DWE303 Withdrawn
DWE522 Withdrawn
DWK506LA35 Size X-LARGE Withdrawn
DWK405LA25S Size LARGE Withdrawn
DWK405LA15S Size LARGE Withdrawn
DWE421 Withdrawn
DWE501 Withdrawn
DWK404LA35S Angle 35 ° Withdrawn
DWK503RA35 Angle 35 ° Withdrawn
DWK403RA35S Size SMALL Withdrawn
DWK404LA15S Angle 15 ° Withdrawn
DWK504RA25 Size MEDIUM Withdrawn
DWK404LA25S Size MEDIUM Withdrawn
DWK404LA35 Size MEDIUM Withdrawn
DWK405LA15 Angle 15 ° Withdrawn
DWK406RA25S Angle 25 ° Withdrawn
DWK406RA15S Angle 15 ° Withdrawn
DWK505RA35 Angle 35 ° Withdrawn
DWK405LA25 Angle 25 ° Withdrawn
DWK503LA35 Size SMALL Withdrawn
DWK503LA25 Angle 25 ° Withdrawn
DWK403RA25 Size SMALL Withdrawn
DWK506LA25 Size X-LARGE Withdrawn
DWK404LA25 Angle 25 ° Withdrawn
DWE533 Withdrawn
DWE503 Withdrawn
DWE313 Withdrawn
DWK403RA35 Angle 35 ° Withdrawn
DWE412 Withdrawn
DWE513 Withdrawn
DWK505LA15 Angle 15 ° Withdrawn
DWK406LA25 Angle 25 ° Withdrawn
DWK505LA25 Angle 25 ° Withdrawn
DWE531 Withdrawn
DWE532 Withdrawn
DWK405RA25S Angle 25 ° Withdrawn
DWK505RA15 Angle 15 ° Withdrawn
DWK406LA25S Angle 25 ° Withdrawn
DWK406RA25 Angle 25 ° Withdrawn
DWK406LA15 Size X-LARGE Withdrawn
DWE512 Withdrawn
DWK403RA15S Size SMALL Withdrawn
DWK406LA15S Size X-LARGE Withdrawn
DWK404RA25S Size MEDIUM Withdrawn
DWE502 Withdrawn
DWE322 Withdrawn
DWK406LA35 Size X-LARGE Withdrawn
DWK404RA35S Size MEDIUM Withdrawn
DWK403RA25S Size SMALL Withdrawn
DWK506RA35 Angle 35 ° Withdrawn
DWK403LA25S Angle 25 ° Withdrawn
DWE312 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™ Ascend™ Flex Tornier Inc. 102
Anatomic Shoulder Prosthesis Medacta International SA 90
Cofield Smith & Nephew, Inc. 76

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
K260721 2026-07-22
K191318 2019-06-14
K181420 2018-09-20
K160975 2016-06-10
K150583 2015-04-23
K121493 2012-06-20
K120794 2012-04-13
K113413 2012-03-09
K111902 2011-11-03
K110865 2011-04-27
K102924 2011-01-31
K103007 2010-11-09
K082120 2008-10-24
K081707 2008-07-17
K060209 2006-03-02
K043077 2004-12-17
K041339 2004-06-17
K032679 2003-12-15
K012212 2001-08-15
K003728 2000-12-20
K994393 2000-06-22
K994392 2000-03-10
K980244 1999-08-23
K952928 1995-09-27

Recalls

6 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
2026-03-05 Class II Labeling design Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system. 233
2025-12-19 Class II Labeling mix-ups A specific lot of screws is incorrectly labeled. Screws are labeled as 5.0mmx18mm but actual screws are 5.00mmx14mm. If mismatch is detected during surgery, the issue may cause a minor delay in surgery. If not detected and incorrect screw i 427
2023-06-12 Class II Under Investigation by firm A comingle/swap resulted in the labeling and laser marking on the product to state it is a Aequalis Flex Revive Assembly Screw 0mm Standard (ARS655101) but it was a Aequalis Flex Revive Assembly Screw 0mm Short (ARS655118) & vice versa. 55 units
2023-06-12 Class II Under Investigation by firm A comingle/swap resulted in the labeling and laser marking on the product to state it is a Aequalis Flex Revive Assembly Screw 0mm Standard (ARS655101) but it was a Aequalis Flex Revive Assembly Screw 0mm Short (ARS655118) & vice versa. 55 units
2021-05-28 Class II Employee error Two lots have been swapped thus have the incorrect product in the package. The component may be of a different thickness. 20 2023-04-14
2016-09-19 Class II Component design/selection Tornier is conducting a recall on Aequalis Fx2 ( implant parts and instrument trays) due to reports of dislocations of the poly insert and the stem. 30 2018-05-31

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