FDA device listing
Cheek retractor,Periotomes GRM 1/GRM 2,Retractors curved,Retractors straight
FDA device listing 2037634110 · SHANGHAI KANGQIAO DENTAL INSTRUMENTS FACTORY
Key facts
| Proprietary names | Cheek retractor,Periotomes GRM 1/GRM 2,Retractors curved,Retractors straight |
|---|---|
| Owner/operator | SHANGHAI KANGQIAO DENTAL INSTRUMENTS FACTORY |
| Owner/operator number | 9070000 |
| Product codes | EIG |
| Device names | EIG - Retractor, All Types |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4565 |
| Review panels | Dental |
| Registered establishments | SHANGHAI KANGQIAO DENTAL INSTRUMENTS FACTORY |
| Establishment registrations | 3004992978 |
| FEI numbers | 3004992978 |
| 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