FDA device listing
HEAT VIBRATION MASSAGER,HEAT VIBRATION REVIVING MASSAGER
FDA device listing 1529508836 · Shenzhen Goodwind Technology Development CO., LTD
Key facts
| Proprietary names | HEAT VIBRATION MASSAGER,HEAT VIBRATION REVIVING MASSAGER |
|---|---|
| Owner/operator | Shenzhen Goodwind Technology Development CO., LTD |
| Owner/operator number | 10046014 |
| 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 | Shenzhen Goodwind Technology Development CO., LTD |
| Establishment registrations | 3010677917 |
| FEI numbers | 3010677917 |
| 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