FDA device listing
FORCEPS
FDA device listing 1455713232 · Rumex International Co.
Key facts
| Proprietary names | FORCEPS |
|---|---|
| Owner/operator | Rumex International Co. |
| Owner/operator number | 9011770 |
| Product codes | GEN |
| Device names | GEN - Forceps, General & Plastic Surgery |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Perfect Ophthalmic Instruments FZE, RUMEX Baltics SIA, RUMEX INTERNATIONAL CO. |
| Establishment registrations | 1058726, 3012185136, 3031231776 |
| FEI numbers | 1000307733, 3012185136, 3031231776 |
| Establishment operations | Manufacturer, Repackager/Relabeler |
| 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