FDA device listing
Costa Del Mar Sunglasses, Inc.,Native Eyewear, Inc.
FDA device listing 1720754853 · EssilorLuxottica
Key facts
| Proprietary names | Costa Del Mar Sunglasses, Inc.,Native Eyewear, Inc. |
|---|---|
| Owner/operator | EssilorLuxottica |
| Owner/operator number | 1035170 |
| Product codes | HQZ |
| Device names | HQZ - Frame, Spectacle |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.5842 |
| Review panels | Ophthalmic |
| Registered establishments | COSTA DEL MAR SUNGLASSES, INC. |
| Establishment registrations | 1052217 |
| FEI numbers | 1052217 |
| Establishment operations | 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