FDA device listing
RESTORATIVE LAB - 3D Printed All on X,RESTORATIVE LAB - 3D Printed Bridges,RESTORATIVE LAB - 3D Printed…
FDA device listing 2057047726 · RESTORATIVE LAB SpA
Key facts
| Proprietary names | RESTORATIVE LAB - 3D Printed All on X,RESTORATIVE LAB - 3D Printed Bridges,RESTORATIVE LAB - 3D Printed Crowns,RESTORATIVE LAB - 3D Printed Guides,RESTORATIVE LAB - 3D Printed Model,RESTORATIVE LAB - 3D Printed Veneer |
|---|---|
| Owner/operator | RESTORATIVE LAB SpA |
| Owner/operator number | 10094116 |
| Product codes | EBH |
| Device names | EBH - Material, Impression Tray, Resin |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.3670 |
| Review panels | Dental |
| Registered establishments | RESTORATIVE LAB SPA |
| Establishment registrations | 3042849555 |
| FEI numbers | 3042849555 |
| Establishment operations | Contract Manufacturer, 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