FDA device listing
FLNTScan R1;FLNTScan R1 Pro;FLNTScan R1 Cart;FLNTScan R2;FLNTScan R2 Pro;FLNTScan R2 Air;FLNTScan R2 Pod;FLNTScan R2 Car
FDA device listing 2003756634 · Liaoning Upcera Co., Ltd
Key facts
| Proprietary names | FLNTScan R1;FLNTScan R1 Pro;FLNTScan R1 Cart;FLNTScan R2;FLNTScan R2 Pro;FLNTScan R2 Air;FLNTScan R2 Pod;FLNTScan R2 Car |
|---|---|
| Owner/operator | Liaoning Upcera Co., Ltd |
| Owner/operator number | 10031628 |
| Product codes | NOF |
| Device names | NOF - System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.3661 |
| Review panels | Dental |
| Registered establishments | Liaoning Upcera Co.,Ltd |
| Establishment registrations | 3008254125 |
| FEI numbers | 3008254125 |
| Establishment operations | Foreign Private Label Distributor |
| 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