FDA device listing
Disposable Traps, Plastic Retainer Denture, Cuspidor Strainer
FDA device listing 1665686810 · Shanghai smedent medical instrument co., ltd.
Key facts
| Proprietary names | Disposable Traps, Plastic Retainer Denture, Cuspidor Strainer |
|---|---|
| Owner/operator | Shanghai smedent medical instrument co., ltd. |
| Owner/operator number | 10051351 |
| Product codes | EKH |
| Device names | EKH - Carver, Dental Amalgam, Operative |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4565 |
| Review panels | Dental |
| Registered establishments | SHANGHAI SMEDENT MEDICAL INSTRUMENT CO., LTD |
| Establishment registrations | 3008370577 |
| FEI numbers | 3008370577 |
| Establishment operations | Foreign Private Label Distributor, 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