FDA device listing
Retainer, Matrix
FDA device listing 1475227183 · Medical Devices Group Limited
Key facts
| Owner/operator | Medical Devices Group Limited |
|---|---|
| Owner/operator number | 10078224 |
| Product codes | JEP |
| Device names | JEP - Retainer, Matrix |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4565 |
| Review panels | Dental |
| Registered establishments | MEDICAL DEVICES GROUP LIMITED |
| Establishment registrations | 3017759006 |
| FEI numbers | 3017759006 |
| 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