FDA device listing
Skincare rejuvenation, SM9003, SM9005,SonicLift,VITERA WAVE+ RED LIGHT THERAPY NIR • ULTRASOUND
FDA device listing 1727434046 · Hong Qiangxing (Shen Zhen) Electronics Limited
Key facts
| Proprietary names | Skincare rejuvenation, SM9003, SM9005,SonicLift,VITERA WAVE+ RED LIGHT THERAPY NIR • ULTRASOUND |
|---|---|
| Owner/operator | Hong Qiangxing (Shen Zhen) Electronics Limited |
| Owner/operator number | 10044280 |
| Product codes | KDQ |
| Device names | KDQ - Bottle, Collection, Vacuum |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.6740 |
| Review panels | General Hospital |
| Registered establishments | HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED |
| Establishment registrations | 3010402752 |
| FEI numbers | 3010402752 |
| 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