FDA device listing
Sunglasses (Non-Prescription Including Photosensitive)
FDA device listing 1519210929 · Goertek Inc
Key facts
| Owner/operator | Goertek Inc |
|---|---|
| Owner/operator number | 10052631 |
| Product codes | HQY |
| Device names | HQY - Sunglasses (Non-Prescription Including Photosensitive) |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.5850 |
| Review panels | Ophthalmic |
| Registered establishments | Goertek Inc, Goertek Smart Technology Vina Co.,Ltd., GOERTEK TECHNOLOGY VINA CO.,LTD, Qingdao Goertek Horizons Technology Co., Ltd., WEIFANG GOERTEK ELECTRONICS CO., LTD. |
| Establishment registrations | 3012981754, 3017122860, 3037611336, 3039431671, 3046005946 |
| FEI numbers | 3012981754, 3017122860, 3037611336, 3039431671, 3046005946 |
| Establishment operations | Contract Manufacturer, 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