FDA device listing
Emerald Herbst
FDA device listing 1980208850 · MODERN DENTAL LABORATORY CO.LTD.
Key facts
| Proprietary names | Emerald Herbst |
|---|---|
| Owner/operator | MODERN DENTAL LABORATORY CO.LTD. |
| Owner/operator number | 9059261 |
| Premarket submissions | K223624 |
| Product codes | LQZ, LRK |
| Device names | LQZ - Device, Jaw Repositioning, LRK - Device, Anti-Snoring |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.5570 |
| Review panels | Dental |
| Registered establishments | Modern Dental Global Solutions Limited, Modern Dental International Trading Limited, Modern Dental Laboratory (DG) Co., Ltd. |
| Establishment registrations | 3010022489, 3013950969, 3015674959 |
| FEI numbers | 3010022489, 3013950969, 3015674959 |
| Establishment operations | Contract Manufacturer, Foreign Exporter |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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