FDA device listing
Keels,OSCILLATING SAW BLADE,Procedure Pack,Raps,RECIPROCATING SAW BLADE,STABLECUT
FDA device listing 1242232278 · ZIMMER, INC.
Key facts
| Proprietary names | Keels,OSCILLATING SAW BLADE,Procedure Pack,Raps,RECIPROCATING SAW BLADE,STABLECUT |
|---|---|
| Owner/operator | ZIMMER, INC. |
| Owner/operator number | 1822565 |
| Product codes | GFA |
| Device names | GFA - Blade, Saw, General & Plastic Surgery, Surgical |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4820 |
| Review panels | General & Plastic Surgery |
| Registered establishments | ZIMMER, INC., ZIMMER SURGICAL, INC. |
| Establishment registrations | 1526350, 1822565 |
| FEI numbers | 1526350, 1000220733 |
| 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