FDA device listing
Headband
FDA device listing 1357724581 · Yangzhou Jindu Sporting Goods CO., Ltd.
Key facts
| Proprietary names | Headband |
|---|---|
| Owner/operator | Yangzhou Jindu Sporting Goods CO., Ltd. |
| Owner/operator number | 10056372 |
| Product codes | FQM |
| Device names | FQM - Bandage, Elastic |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.5075 |
| Review panels | General Hospital |
| Registered establishments | YANGZHOU JINDU SPORTING GOODS CO., LTD. |
| Establishment registrations | 3013857401 |
| FEI numbers | 3013857401 |
| 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