FDA device listing
Dentures, Partial
FDA device listing 2004901960 · Tin Lok (Dongguan) Dental Laboratory Company Limited
Key facts
| Owner/operator | Tin Lok (Dongguan) Dental Laboratory Company Limited |
|---|---|
| Owner/operator number | 10022986 |
| Product codes | NSK |
| Device names | NSK - Dentures, Partial |
| Device class | Not classified |
| Classification regulations (21 CFR) | ORCA1.NSK |
| Review panels | Dental |
| Registered establishments | Tin Lok (Dongguan) Dental Laboratory Company Limited |
| Establishment registrations | 3006789403 |
| FEI numbers | 3006789403 |
| Establishment operations | Manufacturer |
| 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