FDA device listing
CMD 24-1132 Promade Shoulder,CMD 24-1224 ProMade Shoulder,CMD 24-1240 ProMade Shoulder,CMD 24-1263 ProMade Shoulder,CMD…
FDA device listing 1363724495 · Limacorporate S.p.A.
Key facts
| Proprietary names | CMD 24-1132 Promade Shoulder,CMD 24-1224 ProMade Shoulder,CMD 24-1240 ProMade Shoulder,CMD 24-1263 ProMade Shoulder,CMD 24-1327 ProMade Shoulder,CMD 24-1347 ProMade Shoulder,CMD 24-1362 ProMade Shoulder,CMD 24-1365 ProMade Shoulder,CMD 24-1375 ProMade Shoulder,CMD 24-1380 ProMade Shoulder,CMD 24-1410 ProMade Shoulder,CMD 24-1422 ProMade Shoulder,CMD 24-1423 ProMade Shoulder,CMD 24-1429 ProMade… |
|---|---|
| Owner/operator | Limacorporate S.p.A. |
| Owner/operator number | 10032506 |
| Product codes | PHX |
| Device names | PHX - Shoulder Prosthesis, Reverse Configuration |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3660 |
| 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