FDA device listing
DePuy Actis Duofix Hip Prosthesis
FDA device listing 1450062105 · SHANGHAI JPY ION-TECH CO., LTD.
Key facts
| Proprietary names | DePuy Actis Duofix Hip Prosthesis |
|---|---|
| Owner/operator | SHANGHAI JPY ION-TECH CO., LTD. |
| Owner/operator number | 9066119 |
| Product codes | KWL, KWY, LPH, MEH |
| Device names | KWL - Prosthesis, Hip, Hemi-, Femoral, Metal, KWY - Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented, LPH - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, MEH - Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3353, 888.3358, 888.3360, 888.3390 |
| Review panels | Orthopedic |
| Registered establishments | SHANGHAI JPY ION-TECH CO., LTD. |
| Establishment registrations | 3004748528 |
| FEI numbers | 3004748528 |
| Establishment operations | Contract Sterilizer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database