Trident
38 catalogue numbers from 500-11-68I, listed by Howmedica Osteonics Corp, United States, under Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer. 10 manufacturers in China are registered for this product code.
10manufacturers in China registered for this device type
38catalogue numbers in this listing
4510(k) clearances naming this product code
1recall
Who Else Makes It
Concentrated in Jiangsu (5), Shanghai (2), Zhejiang (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Canwell Medical Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 42 |
| Suzhou Elite Precision Machinery Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 35 |
| Stryker (Suzhou) Medical Technology Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 19 |
| APS Materials Suzhou | Suzhou | Jiangsu | Contract manufacturer | 18 |
| Xian Airfoil Technology Co., Ltd. | Xian | Shaanxi | Contract manufacturer | 8 |
| Lincotek (Wuxi) Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 7 |
| 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 |
Record
| Listed by | Howmedica Osteonics Corp, United States |
|---|---|
| FDA product code | KWZ |
| Device type | Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3310 |
| Establishment | Contract manufacturer, Contract steriliser, Specification developer, Manufacturer |
| 510(k) | P960047 |
| Record published | 2015-09-24 |
| Record revised | 2025-09-08 (version 5) |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number |
| Sizes | Outer diameter 40 to 80 mm; lumen/inner diameter 22 to 28 mm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 500-11-68I | Alpha Code: I | In distribution |
| 69-2248 | Outer Diameter 48.0 mm | In distribution |
| 69-3256 | Outer Diameter 56.0 mm | In distribution |
| 690-00-32I | Alpha Code: I | In distribution |
| 502-01-56F | Outer Diameter 56.0 mm | In distribution |
| 69-2852 | Outer Diameter 52.0 mm | In distribution |
| 509-02-70I | Outer Diameter 70.0 mm | In distribution |
| 542-11-66I | Outer Diameter 66.0 mm | In distribution |
| 690-10-28H | Alpha Code: H | In distribution |
| 69-2244 | Outer Diameter 44.0 mm | In distribution |
| 500-11-58F | Alpha Code: F | In distribution |
| 690-00-22D | Alpha Code: D | In distribution |
| 502-11-66H | Alpha Code: H | In distribution |
| 500-11-80L | Outer Diameter 80.0 mm | In distribution |
| 69-3258 | Outer Diameter 58.0 mm | In distribution |
| 690-10-28J | Lumen/Inner Diameter 28.0 mm | In distribution |
| 69-3260 | Outer Diameter 60.0 mm | In distribution |
| 540-11-80L | Alpha Code: L | In distribution |
| 690-10-28I | Lumen/Inner Diameter 28.0 mm | In distribution |
| 690-00-28G | Alpha Code: G | In distribution |
| 690-00-28F | Alpha Code: F | In distribution |
| 69-2850 | Outer Diameter 50.0 mm | In distribution |
| 690-00-22E | Alpha Code: E | In distribution |
| 690-10-22E | Lumen/Inner Diameter 22.0 mm | In distribution |
| 509-02-54E | Outer Diameter 54.0 mm | In distribution |
| 690-00-32H | Alpha Code: H | In distribution |
| 540-11-40A | Outer Diameter 40.0 mm | In distribution |
| 69-2854 | Outer Diameter 54.0 mm | In distribution |
| 540-11-52E | Outer Diameter 52.0 mm | In distribution |
| 690-10-28K | Alpha Code: K | In distribution |
| 690-10-22F | Lumen/Inner Diameter 22.0 mm | In distribution |
| 690-00-32J | Alpha Code: J | In distribution |
| 69-2246 | Outer Diameter 46.0 mm | In distribution |
| 502-11-44B | Outer Diameter 44.0 mm | In distribution |
| 540-11-58G | Outer Diameter 58.0 mm | In distribution |
| 690-10-28G | Lumen/Inner Diameter 28.0 mm | In distribution |
| 542-11-54F | Alpha Code: F | In distribution |
| 502-11-78K | Outer Diameter 78.0 mm | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| DJO Surgical | Encore Medical, L.P. | 159 |
| Instrument | Howmedica Osteonics Corp | 139 |
| ZMR® | Zimmer, Inc. | 103 |
| Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer | Zimmer, Inc. | 69 |
| Arcos Modular Revision System | Biomet Orthopedics | 66 |
| Pinnacle | Depuy Orthopaedics, Inc. | 52 |
| System 12 | Howmedica Osteonics Corp | 47 |
| Restoration | Howmedica Osteonics Corp | 46 |
| Redapt | Smith & Nephew, Inc. | 43 |
| R3 | Smith & Nephew, Inc. | 41 |
| Arcos Modular Revision Hip System | Biomet Orthopedics | 37 |
| G7® | Biomet Orthopedics | 37 |
Showing 12 of 165. All products under Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K063445 | 2007-03-08 |
| K063550 | 2007-03-08 |
| K063552 | 2007-03-08 |
| K061654 | 2006-07-07 |
Recalls Naming This Product
2 recalls name this product by its own identifiers, the UDI on its label.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Howmedica Osteonics Corp | UDI-DI | 2026-07-30 | Not classified | Process change control | Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to | 12,156 US |
| Howmedica Osteonics Corp | UDI-DI | 2026-07-30 | Not classified | Process change control | Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to | 12,156 US |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
| PMA number | Decision | Trade name | Approved to |
|---|---|---|---|
| P960054 | 1997-06-19 | S-ROM POLY-DIAL CONSTRAINED LINER | Depuy, A Johnson & Johnson Co. |
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.