FDA device listing
PlasmaMax Pro 8D Multi-Functional Cold & Hot, Light Goddess PRO Therapeutic Skin Revitalizer,Rejuva Fresh Adonis,Rejuva…
FDA device listing 1770924104 · Rejuva Fresh LLC
Key facts
| Proprietary names | PlasmaMax Pro 8D Multi-Functional Cold & Hot, Light Goddess PRO Therapeutic Skin Revitalizer,Rejuva Fresh Adonis,Rejuva Fresh CaviTONE LEGACY Complete,Rejuva Fresh CelluSpice,Rejuva Fresh CoolRestore Elegance,Rejuva Fresh Diamond Ice,Rejuva Fresh Diamond Ice 360 Degrees Cryo,Rejuva Fresh Eris Lipo Cavitation 6 on 1,Rejuva Fresh Eris Lipo Cavitation 9 on 1,Rejuva Fresh FlowWave FOCUS,Rejuva Fresh… |
|---|---|
| Owner/operator | Rejuva Fresh LLC |
| Owner/operator number | 10091638 |
| 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 | REJUVA FRESH LLC |
| Establishment registrations | 3033844600 |
| FEI numbers | 3033844600 |
| 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