FDA device listing
Alain Mikli,Armani,Arnette,Brooks Brothers,Bulgari,Burberry,Chanel,Chaps,Coach,Disney,DKNY,Dolce & Gabbana,Donna Karan…
FDA device listing 1519456426 · Oakley
Key facts
| Proprietary names | Alain Mikli,Armani,Arnette,Brooks Brothers,Bulgari,Burberry,Chanel,Chaps,Coach,Disney,DKNY,Dolce & Gabbana,Donna Karan eyewear,Eye Safety Systems (ESS),Fox Eyewear,K&L,Michael Kors,Miu Miu,Oakley,Oliver Peoples,Paul Smith Spectacles,Persol,Polo Ralph Lauren,Prada,Ralph Lauren,Ralph Lauren Purple Label,Ray-Ban,Reed Krakoff,Revo,Sferoflex,Stella McCartney,Tiffany & Co.,Tory… |
|---|---|
| Owner/operator | Oakley |
| Owner/operator number | 10056263 |
| Product codes | HQZ |
| Device names | HQZ - Frame, Spectacle |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.5842 |
| Review panels | Ophthalmic |
| Registered establishments | Luxottica After Sales Canada |
| Establishment registrations | 3012879963 |
| FEI numbers | 3012879963 |
| Establishment operations | Foreign Private Label Distributor, Repackager/Relabeler |
| 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