FDA device listing
Removable partial, teething
FDA device listing 1196088603 · Shenzhen Robust Dental Laboratory Co., Limited
Key facts
| Proprietary names | Removable partial, teething |
|---|---|
| Owner/operator | Shenzhen Robust Dental Laboratory Co., Limited |
| Owner/operator number | 10086065 |
| Product codes | MEF |
| Device names | MEF - Ring, Teething, Non-Fluid Filled |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.5550 |
| Review panels | Dental |
| Registered establishments | SHENZHEN ROBUST DENTAL LABORATORY CO., LIMITED |
| Establishment registrations | 3025358043 |
| FEI numbers | 3025358043 |
| Establishment operations | Foreign Exporter, Manufacturer |
| 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