FDA device listing
Light Based Over The Counter Wrinkle Reduction
FDA device listing 1027487589 · GYMMAX TECHNOLOGY SHENZHEN CO., LTD.
Key facts
| Owner/operator | GYMMAX TECHNOLOGY SHENZHEN CO., LTD. |
|---|---|
| Owner/operator number | 10027514 |
| Product codes | OHS |
| Device names | OHS - Light Based Over The Counter Wrinkle Reduction |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4810 |
| Review panels | General & Plastic Surgery |
| Registered establishments | GYMMAX TECHNOLOGY SHENZHEN CO., LTD |
| Establishment registrations | 3007689716 |
| FEI numbers | 3007689716 |
| 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