FDA device listing
Anti-Fog Visor, Anti-Fog Glasses
FDA device listing 1988240004 · Zhejiang Wellong Medical Technology Co., Ltd
Key facts
| Proprietary names | Anti-Fog Visor, Anti-Fog Glasses |
|---|---|
| Owner/operator | Zhejiang Wellong Medical Technology Co., Ltd |
| Owner/operator number | 9052133 |
| Product codes | HOY |
| Device names | HOY - Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.4750 |
| Review panels | Ophthalmic |
| Registered establishments | Zhejiang Wellong Medical Technology Co., Ltd |
| Establishment registrations | 3003835287 |
| FEI numbers | 3003835287 |
| 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