FDA device listing
TECNIDENT EQUIPAMENTOS ORTODONTICOS
FDA device listing 1608332629 · TECNIDENT EQUIPAMENTOS ORTODONTICOS LTDA.
Key facts
| Proprietary names | TECNIDENT EQUIPAMENTOS ORTODONTICOS |
|---|---|
| Owner/operator | TECNIDENT EQUIPAMENTOS ORTODONTICOS LTDA. |
| Owner/operator number | 9055367 |
| Product codes | ECP |
| Device names | ECP - Instrument, Ligature Tucking, Orthodontic |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4565 |
| Review panels | Dental |
| Registered establishments | TECNIDENT EQUIPAMENTOS ORTODONTICOS LTDA. |
| Establishment registrations | 3003092374 |
| FEI numbers | 3003092374 |
| Establishment operations | Foreign Exporter, Manufacturer, Repackager/Relabeler |
| 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