FDA device listing
SHOFU RESIN GLAZE
FDA device listing 1347710973 · SHOFU INC.
Key facts
| Proprietary names | SHOFU RESIN GLAZE |
|---|---|
| Owner/operator | SHOFU INC. |
| Owner/operator number | 9056340 |
| Premarket submissions | K163568 |
| Product codes | EBD |
| Device names | EBD - Coating, Filling Material, Resin |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.3310 |
| Review panels | Dental |
| Registered establishments | SHOFU DENTAL CORP., SHOFU INC. |
| Establishment registrations | 2916735, 3002808149 |
| FEI numbers | 2916735, 3002808149 |
| Establishment operations | Manufacturer, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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