FDA device listing
DermaSound Ultra Skin Scrubber,EpiWave Skin Scrubber,KUS-028 Portable Skin Scrubber,KUS-048 Portable Magic Scrub,KUS-103…
FDA device listing 1573944810 · KING ULTRASONIC CO., LTD.
Key facts
| Proprietary names | DermaSound Ultra Skin Scrubber,EpiWave Skin Scrubber,KUS-028 Portable Skin Scrubber,KUS-048 Portable Magic Scrub,KUS-103 Skin Scrubber,KUS-2000 Skin Scrubber,LM1401 Skin Perfecter,MEDIWAVE skin scrubber,UD-039 Portable Skin Cleaner,XSENSIA skin scrubber |
|---|---|
| Owner/operator | KING ULTRASONIC CO., LTD. |
| Owner/operator number | 9039108 |
| Product codes | GFE |
| Device names | GFE - Brush, Dermabrasion, Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4820 |
| Review panels | General & Plastic Surgery |
| Registered establishments | KING ULTRASONIC CO., LTD. |
| Establishment registrations | 9615076 |
| FEI numbers | 3002775750 |
| 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