FDA device listing
VX130,VX130+
FDA device listing 1747772817 · LUNEAU TECHNOLOGY OPERATIONS
Key facts
| Proprietary names | VX130,VX130+ |
|---|---|
| Owner/operator | LUNEAU TECHNOLOGY OPERATIONS |
| Owner/operator number | 8020811 |
| Premarket submissions | K162067 |
| Product codes | HKX, MXK |
| Device names | HKX - Tonometer, Ac-Powered, MXK - Device, Analysis, Anterior Segment |
| Device class | Class II |
| Classification regulations (21 CFR) | 886.1850, 886.1930 |
| Review panels | Ophthalmic |
| Registered establishments | LUNEAU TECHNOLOGY OPERATIONS, VISIONIX LTD. |
| Establishment registrations | 3003771740, 3009173773 |
| FEI numbers | 3003771740, 3009173773 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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