FDA device listing
Attachment Template
FDA device listing 1990406437 · Wuxi EA Medical Instruments Technologies Limited
Key facts
| Proprietary names | Attachment Template |
|---|---|
| Owner/operator | Wuxi EA Medical Instruments Technologies Limited |
| Owner/operator number | 10060304 |
| Product codes | QJJ |
| Device names | QJJ - Indirect Bonding Tray |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.5410 |
| Review panels | Dental |
| Registered establishments | WUXI EA MEDICAL INSTRUMENTS TECHNOLOGIES LIMITED |
| Establishment registrations | 3013556527 |
| FEI numbers | 3013556527 |
| 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