FDA device listing
Limb Orthosis
FDA device listing 1087508390 · PROFESSIONAL PRODUCTS, INC.
Key facts
| Proprietary names | Limb Orthosis |
|---|---|
| Owner/operator | PROFESSIONAL PRODUCTS, INC. |
| Owner/operator number | 1026765 |
| Product codes | IQI |
| Device names | IQI - Orthosis, Limb Brace |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | PROFESSIONAL PRODUCTS, INC. |
| Establishment registrations | 1026765 |
| FEI numbers | 1026765 |
| Establishment operations | 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