FDA device listing
Anchor Drill,Bone Flat Drill,Core Drill,Cortical Drill,Final Drill,Guide Final Drill,Guide Initial Drill,Guide Path…
FDA device listing 2056465795 · DIMPLO Ltd.
Key facts
| Proprietary names | Anchor Drill,Bone Flat Drill,Core Drill,Cortical Drill,Final Drill,Guide Final Drill,Guide Initial Drill,Guide Path Drill,Guide Sinus Final Drill,Guide Sinus Round Drill,Guide Socket Drill,Guide Step Drill,Initial Drill,Lance Drill,Round Drill,Sidecut Drill,Taper Drill,Twist Drill |
|---|---|
| Owner/operator | DIMPLO Ltd. |
| Owner/operator number | 10094913 |
| Product codes | DZA |
| Device names | DZA - Drill, Dental, Intraoral |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4130 |
| Review panels | Dental |
| Registered establishments | DIMPLO Ltd. |
| Establishment registrations | 3042971970 |
| FEI numbers | 3042971970 |
| Establishment operations | 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