FDA device listing
Implant, Endosseous, Root-Form
FDA device listing 2051589804 · Rickli Micromecanique SA
Key facts
| Owner/operator | Rickli Micromecanique SA |
|---|---|
| Owner/operator number | 10051272 |
| Product codes | DZE |
| Device names | DZE - Implant, Endosseous, Root-Form |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.3640 |
| Review panels | Dental |
| Registered establishments | RICKLI MICROMECANIQUE SA |
| Establishment registrations | 3002963873 |
| FEI numbers | 3002963873 |
| Establishment operations | Contract 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