FDA device listing
Toothbrush, Manual
FDA device listing 1103010430 · Procter & Gamble
Key facts
| Owner/operator | Procter & Gamble |
|---|---|
| Owner/operator number | 9915005 |
| Product codes | EFW |
| Device names | EFW - Toothbrush, Manual |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.6855 |
| Review panels | Dental |
| Registered establishments | Beijing Technology Co - Innovation Center, BRAUN GMBH, BRAUN (SHANGHAI) CO., LTD., Gillette Diversified Operations (P) Ltd, ORAL-B LABORATORIES, PROCTER & GAMBLE DISTRIBUTING LLC, THE, Procter & Gamble Manufacturing Mexico S. de R.L. de C.V., The Procter & Gamble Distributing LLC |
| Establishment registrations | 1910469, 9617642, 9710651, 3002485596, 3007817025, 3011964664, 3021636076, 3030192581 |
| FEI numbers | 1910469, 1000227535, 3001605950, 3002485596, 3007817025, 3011964664, 3021636076, 3030192581 |
| Establishment operations | Foreign Exporter, 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