FDA device listing
UF(II) Cylinder Screw,UF(II) Eastab Cylinder,UF(II) Eastab Cylinder Semi Final,UF(II) Eco Angled Post,UF(II) Eco Base…
FDA device listing 1657196528 · DIO Corporation
Key facts
| Proprietary names | UF(II) Cylinder Screw,UF(II) Eastab Cylinder,UF(II) Eastab Cylinder Semi Final,UF(II) Eco Angled Post,UF(II) Eco Base Abutment,UF(II) Eco Base Screw,UF(II) Eco Cemented Post,UF(II) Eco Healing Cap,UF(II) Eco Post Screw,UF(II) Eco Temporary Post,UF(II) Healing Cap,UF(II) Multi Angled Abutment,UF(II) Multi Straight Abutment,UF(II) Temporary Cylinder,UF(II) Temporary Cylinder Semi Final |
|---|---|
| Owner/operator | DIO Corporation |
| Owner/operator number | 9089142 |
| Premarket submissions | K220253 |
| Product codes | NHA |
| Device names | NHA - Abutment, Implant, Dental, Endosseous |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.3630 |
| Review panels | Dental |
| Registered establishments | DIO Corporation |
| Establishment registrations | 3007126709 |
| FEI numbers | 3007126709 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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