FDA device listing
Kegel Ball
FDA device listing 1809242333 · Xi'an Furuize Biotechnology Co., Ltd.
Key facts
| Proprietary names | Kegel Ball |
|---|---|
| Owner/operator | Xi'an Furuize Biotechnology Co., Ltd. |
| Owner/operator number | 10061640 |
| Product codes | KXQ |
| Device names | KXQ - Vibrator For Therapeutic Use, Genital |
| Device class | Class II |
| Classification regulations (21 CFR) | 884.5960 |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | XI'AN FURUIZE BIOTECHNOLOGY CO., LTD. |
| Establishment registrations | 3016171962 |
| FEI numbers | 3016171962 |
| 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