FDA device listing
Ice Cooling IPL Hair Removal Device,MI01 LP, MI01 CB, MI01 GR, MI01 PP, MI01 RM, MI01 WG, MI01 WH, MI01 BK,Model(s)…
FDA device listing 1641386803 · ULIKE COMPANY LIMITED
Key facts
| Proprietary names | Ice Cooling IPL Hair Removal Device,MI01 LP, MI01 CB, MI01 GR, MI01 PP, MI01 RM, MI01 WG, MI01 WH, MI01 BK,Model(s): UI20S BS, UI20S DB, UI20S GP, UI20S GR, UI20S MP, UI20S PW, UI20S RE, UI20S WH, UI20 WG,UI04 MK, UI04 BN, UI04 BU, UI04 CB, UI04 GY, UI04 LG, UI04 DG, UI04 PL, UI04 PN, UI04 SD, UI04 SG, UI04 MG; UI04S PP,,UI04S BU, UI04S WH, UI04S PN,UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB,UI06… |
|---|---|
| Owner/operator | ULIKE COMPANY LIMITED |
| Owner/operator number | 10090489 |
| Product codes | OHT |
| Device names | OHT - Light Based Over-The-Counter Hair Removal |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4810 |
| Review panels | General & Plastic Surgery |
| Registered establishments | ULIKE COMPANY LIMITED |
| Establishment registrations | 3029944286 |
| FEI numbers | 3029944286 |
| Establishment operations | Contract 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