FDA device listing
MemoMind One, Smart Glasses, MM001
FDA device listing 1703129318 · Shenzhen Qinglai Innovation Technology Co., Ltd.
Key facts
| Proprietary names | MemoMind One, Smart Glasses, MM001 |
|---|---|
| Owner/operator | Shenzhen Qinglai Innovation Technology Co., Ltd. |
| Owner/operator number | 10096255 |
| 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 | Shenzhen Qinglai Innovative Intelligent Technology Co., Ltd. |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- None 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