FDA device listing
Retainer, Screw Expansion, Orthodontic
FDA device listing 1146164879 · Ortho Solutions LC
Key facts
| Owner/operator | Ortho Solutions LC |
|---|---|
| Owner/operator number | 1937100 |
| Product codes | DYJ |
| Device names | DYJ - Retainer, Screw Expansion, Orthodontic |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.5410 |
| Review panels | Dental |
| Registered establishments | Ortho Solutions LC |
| Establishment registrations | 1937100 |
| FEI numbers | 1937100 |
| Establishment operations | 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