FDA device listing
Keratoscope, Ac-Powered
FDA device listing 1784030362 · NIDEK CO., LTD.
Key facts
| Owner/operator | NIDEK CO., LTD. |
|---|---|
| Owner/operator number | 8030392 |
| Product codes | HLQ |
| Device names | HLQ - Keratoscope, Ac-Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.1350 |
| Review panels | Ophthalmic |
| Registered establishments | NIDEK CO., LTD., NIDEK CO., LTD. HAMACHO PLANT, NIDEK INCORPORATED |
| Establishment registrations | 2936921, 8030392, 3002807715 |
| FEI numbers | 2936921, 3002807715 |
| Establishment operations | Manufacturer, Specification Developer |
| 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