Perform™ Humeral System
33 catalogue numbers from DWN3713, listed by Tornier Inc., United States, under Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented. 9 manufacturers in China are registered for this product code.
9manufacturers in China registered for this device type
33catalogue 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.
| 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
| 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 | 2020-11-10 |
| Record revised | 2026-02-11 (version 3) |
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 | Height 13 to 27 mm; outer diameter 37 to 56 mm |
| Distribution end date | 2022-04-07 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| DWN3713 | Height 13.5 mm | Withdrawn |
| DWN4113 | Height 13.5 mm | Withdrawn |
| DWX3SS | Size 3 | Withdrawn |
| DWT4820 | Height 20 mm | Withdrawn |
| DWN4617 | Outer Diameter 46 mm | Withdrawn |
| DWX2SS | Size 2 | Withdrawn |
| DWN5427 | Outer Diameter 54 mm | Withdrawn |
| DWN5424 | Outer Diameter 54 mm | Withdrawn |
| DWT5219 | Outer Diameter 52 mm | Withdrawn |
| DWN4314 | Height 14 mm | Withdrawn |
| DWN4115 | Height 15 mm | Withdrawn |
| DWT5625 | Outer Diameter 56 mm | Withdrawn |
| DWN5420 | Height 20 mm | Withdrawn |
| DWN5016 | Height 16 mm | Withdrawn |
| DWX1PL | Size 1+ | Withdrawn |
| DWT3713 | Height 13.5 mm | Withdrawn |
| DWT5420 | Height 20 mm | Withdrawn |
| DWN5219 | Outer Diameter 52 mm | Withdrawn |
| DWT5223 | Height 23 mm | Withdrawn |
| DWX3PL | Size 3+ | Withdrawn |
| DWN3913 | Height 13 mm | Withdrawn |
| DWN3915 | Outer Diameter 39 mm | Withdrawn |
| DWT5622 | Height 22 mm | Withdrawn |
| DWT4113 | Height 13.5 mm | Withdrawn |
| DWN4820 | Outer Diameter 48 mm | Withdrawn |
| DWN4316 | Outer Diameter 43 mm | Withdrawn |
| DWT5019 | Outer Diameter 50 mm | Withdrawn |
| DWN5019 | Outer Diameter 50 mm | Withdrawn |
| DWT3915 | Height 15 mm | Withdrawn |
| DWT5022 | Outer Diameter 50 mm | Withdrawn |
| DWT4318 | Height 18 mm | Withdrawn |
| DWN4619 | Height 19 mm | Withdrawn |
| DWN5223 | Outer Diameter 52 mm | Withdrawn |
Same 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
| 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.
| 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.