FDA device listing
rubber dam forceps,RUBBER DAM KIT
FDA device listing 1420094023 · WUXI LYUSMILE IMP AND EXP CO.,LTD
Key facts
| Proprietary names | rubber dam forceps,RUBBER DAM KIT |
|---|---|
| Owner/operator | WUXI LYUSMILE IMP AND EXP CO.,LTD |
| Owner/operator number | 10082225 |
| Product codes | EJG |
| Device names | EJG - Forceps, Rubber Dam Clamp |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.6300 |
| Review panels | Dental |
| Registered establishments | WUXI LYUSMILE IMP AND EXP CO.,LTD |
| Establishment registrations | 3021023132 |
| FEI numbers | 3021023132 |
| Establishment operations | Foreign Private Label Distributor |
| 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