FDA device listing
Centellian24 MADECA PRIME MAX,Centellian24 MADECA PRIME RITUAL WHITE PEARL,DERMAURA CORE,DERMAURA PRO
FDA device listing 1016344943 · WITHNIX CO., LTD.
Key facts
| Proprietary names | Centellian24 MADECA PRIME MAX,Centellian24 MADECA PRIME RITUAL WHITE PEARL,DERMAURA CORE,DERMAURA PRO |
|---|---|
| Owner/operator | WITHNIX CO., LTD. |
| Owner/operator number | 10094285 |
| 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 | WITHNIX CO., LTD. |
| Establishment registrations | 3020750249 |
| FEI numbers | 3020750249 |
| 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