FDA device listing
CMD 24-1584 ProMade Hip,CMD 24-1603 ProMade Hip,CMD 24-1610 ProMade Hip,CMD 24-1641 ProMade Hip,CMD 25-1053 ProMade…
FDA device listing 1714806538 · Limacorporate S.p.A.
Key facts
| Proprietary names | CMD 24-1584 ProMade Hip,CMD 24-1603 ProMade Hip,CMD 24-1610 ProMade Hip,CMD 24-1641 ProMade Hip,CMD 25-1053 ProMade Hip,CMD 25-1075 ProMade Hip,CMD 25-1081 ProMade Hip,CMD 25-1083 ProMade Hip,CMD 25-1131 ProMade Hip,CMD 25-1137 ProMade Hip,CMD 25-1207 ProMade Hip,CMD 25-1228 ProMade Hip,CMD 25-1238 ProMade Hip,CMD 25-1271 ProMade Hip,CMD 25-1290 ProMade Hip,CMD 25-1313 ProMade Hip,CMD 25-1362… |
|---|---|
| Owner/operator | Limacorporate S.p.A. |
| Owner/operator number | 10032506 |
| Product codes | LPH |
| Device names | LPH - Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3358 |
| Review panels | Orthopedic |
| Registered establishments | Limacorporate S.p.A. |
| Establishment registrations | 3008021110, 3008395353 |
| FEI numbers | 3008021110, 3008395353 |
| 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