FDA device listing
Lippo Massager, GLO910,Lippo Massager, GLO910+,Lippo Massager, GLO910 PRO
FDA device listing 2020865260 · MIXEN COMPANY LIMITED
Key facts
| Proprietary names | Lippo Massager, GLO910,Lippo Massager, GLO910+,Lippo Massager, GLO910 PRO |
|---|---|
| Owner/operator | MIXEN COMPANY LIMITED |
| Owner/operator number | 10053270 |
| 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 | MIXEN COMPANY LIMITED |
| Establishment registrations | 3013510855 |
| FEI numbers | 3013510855 |
| 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