FDA device listing
3DMaxx Scanner,Custom Orthopedic Braces,GEN3 3DMaxx Scanner,Metascan Pressure Mat
FDA device listing 1830733054 · Footmaxx of Virginia
Key facts
| Proprietary names | 3DMaxx Scanner,Custom Orthopedic Braces,GEN3 3DMaxx Scanner,Metascan Pressure Mat |
|---|---|
| Owner/operator | Footmaxx of Virginia |
| Owner/operator number | 10031149 |
| Product codes | IPM |
| Device names | IPM - Cover, Limb |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3025 |
| Review panels | Physical Medicine |
| Registered establishments | Footmaxx of Virginia |
| Establishment registrations | 3009285151 |
| FEI numbers | 3009285151 |
| 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