FDA device listing
Essilor of America,Nassau Vision Group,Shore Lens Company
FDA device listing 1243317354 · CHEMILENS VIETNAM JOINT STOCK COMPANY
Key facts
| Proprietary names | Essilor of America,Nassau Vision Group,Shore Lens Company |
|---|---|
| Owner/operator | CHEMILENS VIETNAM JOINT STOCK COMPANY |
| Owner/operator number | 10053825 |
| Product codes | HQG |
| Device names | HQG - Lens, Spectacle, Non-Custom (Prescription) |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.5844 |
| Review panels | Ophthalmic |
| Registered establishments | CHEMILENS VIETNAM JOINT STOCK COMPANY |
| Establishment registrations | 3013232890 |
| FEI numbers | 3013232890 |
| Establishment operations | Contract Manufacturer, Foreign Exporter, Manufacturer, Remanufacturer |
| 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