Aequalis™ Ascend™ Flex

102 catalogue numbers from DWF708A, 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
102catalogue 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™ Ascend™ Flex
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
Record published 2015-10-16
Record revised 2026-02-13 (version 4)

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 Length 66 to 130 mm; angle 127.5 to 137.5 °
Distribution end date 2022-03-25

Catalogue Numbers

Catalogue numbers for Aequalis™ Ascend™ Flex
Catalogue number Size Status
DWF708A Length 90 mm Withdrawn
DWF618C Size 8C Withdrawn
DWF718C Length 120 mm Withdrawn
DWF609A Length 98 mm Withdrawn
DWF602B Size 2B Withdrawn
DWF713A Length 93 mm Withdrawn
DWF614A Angle 127.5 ° Withdrawn
DWF618B Angle 132.5 ° Withdrawn
DWF618A Length 125 mm Withdrawn
DWF608B Size 8B Withdrawn
DWF611C Size 1C Withdrawn
DWF702C Size 2C Withdrawn
DWF708C Size 8C Withdrawn
DWF712B Angle 132.5 ° Withdrawn
DWF714C Angle 137.5 ° Withdrawn
DWF703C Angle 137.5 ° Withdrawn
DWF604C Angle 137.5 ° Withdrawn
DWF602C Angle 137.5 ° Withdrawn
DWF716B Size 6B Withdrawn
DWF713B Angle 132.5 ° Withdrawn
DWF619B Length 130 mm Withdrawn
DWF704C Size 4C Withdrawn
DWF706B Length 82 mm Withdrawn
DWF603B Angle 132.5 ° Withdrawn
DWF603A Angle 127.5 ° Withdrawn
DWF705A Size 5A Withdrawn
DWF607C Length 90 mm Withdrawn
DWF706A Length 82 mm Withdrawn
DWF609B Size 9B Withdrawn
DWF606A Size 6A Withdrawn
DWF702B Angle 132.5 ° Withdrawn
DWF619C Length 130 mm Withdrawn
DWF601B Angle 132.5 ° Withdrawn
DWF615C Size 5C Withdrawn
DWF613B Size 3B Withdrawn
DWF709C Size 9C Withdrawn
DWF615B Length 109 mm Withdrawn
DWF603C Angle 137.5 ° Withdrawn
DWF612A Length 93 mm Withdrawn
DWF605C Angle 137.5 ° Withdrawn
DWF718B Size 8B Withdrawn
DWF604A Length 78 mm Withdrawn
DWF605B Angle 132.5 ° Withdrawn
DWF705B Angle 132.5 ° Withdrawn
DWF605A Length 82 mm Withdrawn
DWF717C Length 115 mm Withdrawn
DWF614C Length 104 mm Withdrawn
DWF706C Length 82 mm Withdrawn
DWF617A Length 120 mm Withdrawn
DWF616C Size 6C Withdrawn
DWF613C Length 98 mm Withdrawn
DWF612C Angle 137.5 ° Withdrawn
DWF619A Angle 127.5 ° Withdrawn
DWF713C Angle 137.5 ° Withdrawn
DWF703B Length 70 mm Withdrawn
DWF609C Angle 137.5 ° Withdrawn
DWF617C Length 120 mm Withdrawn
DWF616B Angle 132.5 ° Withdrawn
DWF715A Length 104 mm Withdrawn
DWF714A Length 98 mm Withdrawn
DWF601C Length 66 mm Withdrawn
DWF614B Angle 132.5 ° Withdrawn
DWF608C Length 94 mm Withdrawn
DWF606C Length 86 mm Withdrawn
DWF715B Length 104 mm Withdrawn
DWF602A Length 70 mm Withdrawn
DWF707A Size 7A Withdrawn
DWF616A Angle 127.5 ° Withdrawn
DWF617B Angle 132.5 ° Withdrawn
DWF705C Length 78 mm Withdrawn
DWF717B Angle 132.5 ° Withdrawn
DWF716A Length 109 mm Withdrawn
DWF717A Length 115 mm Withdrawn
DWF719C Size 9C Withdrawn
DWF712A Length 88 mm Withdrawn
DWF615A Length 109 mm Withdrawn
DWF601A Angle 127.5 ° Withdrawn
DWF716C Angle 137.5 ° Withdrawn
DWF606B Size 6B Withdrawn
DWF719B Size 9B Withdrawn
DWF707B Angle 132.5 ° Withdrawn
DWF704A Angle 127.5 ° Withdrawn
DWF712C Size 2C Withdrawn
DWF704B Size 4B Withdrawn
DWF709B Length 94 mm Withdrawn
DWF611A Length 88 mm Withdrawn
DWF714B Size 4B Withdrawn
DWF708B Angle 132.5 ° Withdrawn
DWF607B Length 90 mm Withdrawn
DWF612B Angle 132.5 ° Withdrawn
DWF707C Size 7C Withdrawn
DWF709A Length 94 mm Withdrawn
DWF718A Angle 127.5 ° Withdrawn
DWF702A Length 66 mm Withdrawn
DWF719A Size 9A Withdrawn
DWF608A Size 8A Withdrawn
DWF604B Angle 132.5 ° Withdrawn
DWF607A Angle 127.5 ° Withdrawn
DWF715C Length 104 mm Withdrawn
DWF611B Length 88 mm Withdrawn
DWF613A Length 98 mm Withdrawn
DWF703A Angle 127.5 ° 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
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