FDA device listing
SCANLAN LISTON DOUBL,SCANLAN PLASTER SHEARS,SCANLAN RIB SHEARS
FDA device listing 1588088239 · SCANLAN INTERNATIONAL, INC.
Key facts
| Proprietary names | SCANLAN LISTON DOUBL,SCANLAN PLASTER SHEARS,SCANLAN RIB SHEARS |
|---|---|
| Owner/operator | SCANLAN INTERNATIONAL, INC. |
| Owner/operator number | 2126670 |
| Product codes | FZT |
| Device names | FZT - Cutter, Surgical |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | SCANLAN INTERNATIONAL, INC. |
| Establishment registrations | 2126670 |
| FEI numbers | 2126670 |
| 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