FDA device listing
Conical Over Post # Large,Conical Over Post # Medium,Conical Over Post # Small,Cylindrical Over Post # 0,8,Cylindrical…
FDA device listing 1995138631 · OVERFIBERS S.R.L
Key facts
| Proprietary names | Conical Over Post # Large,Conical Over Post # Medium,Conical Over Post # Small,Cylindrical Over Post # 0,8,Cylindrical Over Post # 1,0,Cylindrical Over Post # 1,2,Cylindrical Over Post # 1,4,Cylindrical Over Post # 1,6,Cylindrical Over Post Black # 0,8,Cylindrical Over Post Black # 1,0,Cylindrical Over Post Black # 1,2,Cylindrical Over Post Black # 1,4,Cylindrical Over Post Black # 1,6,Duo Over… |
|---|---|
| Owner/operator | OVERFIBERS S.R.L |
| Owner/operator number | 10092618 |
| Product codes | ELR |
| Device names | ELR - Post, Root Canal |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.3810 |
| Review panels | Dental |
| Registered establishments | OVERFIBERS S.R.L |
| Establishment registrations | 3030648980 |
| FEI numbers | 3030648980 |
| Establishment operations | Complaint File Establishment, 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