FDA device listing
2.0 MM FULL RADIUS MINI BLADES, POWER/EP-1, BLUE, 7 CM LONG, PACKAGED 6 PER BOX, STERILE,2.9 MM ABRADER MINI BURRS…
FDA device listing 1376303751 · Smith & Nephew, Inc.
Key facts
| Proprietary names | 2.0 MM FULL RADIUS MINI BLADES, POWER/EP-1, BLUE, 7 CM LONG, PACKAGED 6 PER BOX, STERILE,2.9 MM ABRADER MINI BURRS, POWER/EP-1, ORANGE, PACKAGED 6 PER BOX, STERILE,2.9 MM BARREL ABRADER MINI BURRS, POWER/EP-1, PURPLE, PACKAGED 6 PER BOX, STERILE,2.9 MM CUTTER MINI BLADES, POWER/EP-1, BEIGE, 7 CM LONG, PACKAGED 6 PER BOX, STERILE,2.9 MM FULL RADIUS MINI BLADES RED, POWER/EP-1, 7 CM LONG, PACKAGED 6… |
|---|---|
| Owner/operator | Smith & Nephew, Inc. |
| Owner/operator number | 1020279 |
| Product codes | HAB |
| Device names | HAB - Saw, Powered, And Accessories |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4820 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Smith & Nephew, Inc., SMITH & NEPHEW INC., SMITH & NEPHEW, INC. |
| Establishment registrations | 1020279, 1219602, 1643264, 3003604053, 3007366790, 3038503932 |
| FEI numbers | 1020279, 1219602, 1643264, 3003604053, 3007282753, 3038503932 |
| Establishment operations | Manufacturer, Repackager/Relabeler, Specification Developer |
| 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