FDA device listing
3 Dose Compact Mixer,Compact Vacuum Cement Mixing System,DISPOSABLE MIXING BOWL,Zimmer Power-Mix Vacuum Cement Mixing…
FDA device listing 2059463868 · ZIMMER, INC.
Key facts
| Proprietary names | 3 Dose Compact Mixer,Compact Vacuum Cement Mixing System,DISPOSABLE MIXING BOWL,Zimmer Power-Mix Vacuum Cement Mixing System |
|---|---|
| Owner/operator | ZIMMER, INC. |
| Owner/operator number | 1822565 |
| Product codes | JDZ |
| Device names | JDZ - Mixer, Cement, For Clinical Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4210 |
| Review panels | Orthopedic |
| Registered establishments | ZIMMER, INC., ZIMMER SURGICAL, INC. |
| Establishment registrations | 1526350, 1822565 |
| FEI numbers | 1526350, 1000220733 |
| Establishment operations | Manufacturer |
| 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