FDA device listing
40YKTD325,40YKTD326,40YKTD328,VP-01,BDS 075PH,BDS 3365M,PV25,KB-VP-Black…
FDA device listing 1294333638 · YONGKANG TUDING HARDWARE MANUFACTURE CO., LTD
Key facts
| Proprietary names | 40YKTD325,40YKTD326,40YKTD328,VP-01,BDS 075PH,BDS 3365M,PV25,KB-VP-Black ,CUV30,CUV40,CUV50,UC-2481,UT-2482,Vibration01,BT-VIBE,CUV20,CUV20-01AL,CUV20-02AL,SZJ02,SZJ03,SZJ04 ,VB-001,VB-002,KB-VP-Black,MR-2480B1,MR-2480P1,Foot massager, Foot&calf massager, Foot vibration massager… |
|---|---|
| Owner/operator | YONGKANG TUDING HARDWARE MANUFACTURE CO., LTD |
| Owner/operator number | 10081441 |
| Product codes | ISA |
| Device names | ISA - Massager, Therapeutic, Electric |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5660 |
| Review panels | Physical Medicine |
| Registered establishments | YONGKANG TUDING HARDWARE MANUFACTURE CO., LTD |
| Establishment registrations | 3018995133 |
| FEI numbers | 3018995133 |
| 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