FDA device listing
Injection Site
FDA device listing 1179926188 · Zhejiang Anji Huabu Industrial Co., Ltd.
Key facts
| Proprietary names | Injection Site |
|---|---|
| Owner/operator | Zhejiang Anji Huabu Industrial Co., Ltd. |
| Owner/operator number | 9045080 |
| Product codes | FGY |
| Device names | FGY - Cannula, Injection |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4200 |
| Review panels | General & Plastic Surgery |
| Registered establishments | ZHEJIANG ANJI HUABU INDUSTRIAL CO., LTD. |
| Establishment registrations | 9710020 |
| FEI numbers | 3003340795 |
| Establishment operations | 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