FDA device listing
detox foot patch,Foot pad,foot patch,navel patch,rheumatism patch,slimming patch,warm foot patch
FDA device listing 1103127487 · Tianjin Fuqin Science & Technology CORP., Ltd.
Key facts
| Proprietary names | detox foot patch,Foot pad,foot patch,navel patch,rheumatism patch,slimming patch,warm foot patch |
|---|---|
| Owner/operator | Tianjin Fuqin Science & Technology CORP., Ltd. |
| Owner/operator number | 10048937 |
| Product codes | KGX |
| Device names | KGX - Tape And Bandage, Adhesive |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.5240 |
| Review panels | General Hospital |
| Registered establishments | TIANJIN FUQIN SCIENCE & TECHNOLOGY CORP., LTD. |
| Establishment registrations | 3011526963 |
| FEI numbers | 3011526963 |
| Establishment operations | Contract Manufacturer, 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