FDA device listing
TAPERLOC COMPLETE, SIZE 5 AND 6
FDA device listing 1452403811 · ZIMMER, INC.
Key facts
| Proprietary names | TAPERLOC COMPLETE, SIZE 5 AND 6 |
|---|---|
| Owner/operator | ZIMMER, INC. |
| Owner/operator number | 1822565 |
| Premarket submissions | K103755 |
| Product codes | JDI, JDL, KWA, KWL, KWY, KWZ, LPH, LWJ, LZO, MAY, MEH |
| Device names | JDI - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented, JDL - Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component), KWA - Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component), KWL - Prosthesis, Hip, Hemi-, Femoral, Metal, KWY - Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented, KWZ - Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, LPH - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, LWJ - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented, LZO - Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented, MAY - Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish, MEH - Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate |
| Device class | Class II, Class III |
| Classification regulations (21 CFR) | 888.3310, 888.3320, 888.3330, 888.3350, 888.3353, 888.3358, 888.3360, 888.3390 |
| Review panels | Orthopedic |
| Registered establishments | Zimmer Biomet Canada DFE |
| Establishment registrations | 3012392319 |
| FEI numbers | 3012392319 |
| Establishment operations | Foreign Exporter |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 10–99 Device listings citing the same submission
- Yes 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