FDA device listing
CryoGlow,CryoGlow Plus
FDA device listing 1933055216 · Zhangzhou Easepal Medical Science And Technology Co.,Ltd.
Key facts
| Proprietary names | CryoGlow,CryoGlow Plus |
|---|---|
| Owner/operator | Zhangzhou Easepal Medical Science And Technology Co.,Ltd. |
| Owner/operator number | 10084572 |
| Product codes | OHS, OLP |
| Device names | OHS - Light Based Over The Counter Wrinkle Reduction, OLP - Over-The-Counter Powered Light Based Laser For Acne |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4810 |
| Review panels | General & Plastic Surgery |
| Registered establishments | ZHANGZHOU EASEPAL MEDICAL SCIENCE AND TECHNOLOGY CO.,LTD. |
| Establishment registrations | 3014386328 |
| FEI numbers | 3014386328 |
| 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