FDA device listing
Knee Massager: WS500,Neck Massager:G7 Pro-Fold,Neck Massager:GS500-N,SKG THERAPY DEVIC,Waist Massager:W9Ultra
FDA device listing 2023107768 · SKG Health Technologies Co., LTD
Key facts
| Proprietary names | Knee Massager: WS500,Neck Massager:G7 Pro-Fold,Neck Massager:GS500-N,SKG THERAPY DEVIC,Waist Massager:W9Ultra |
|---|---|
| Owner/operator | SKG Health Technologies Co., LTD |
| Owner/operator number | 10083283 |
| Product codes | ILY |
| Device names | ILY - Lamp, Infrared, Therapeutic Heating |
| Device class | Class II |
| Classification regulations (21 CFR) | 890.5500 |
| Review panels | Physical Medicine |
| Registered establishments | SKG Health Technologies Co., LTD |
| Establishment registrations | 3014601569 |
| FEI numbers | 3014601569 |
| Establishment operations | Contract Manufacturer, Foreign Private Label Distributor, 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