FDA device listing
F3 Anterior Carbon Fiber AFO,F3 Anterior FlexTrim Carbon Fiber AFO,F3 Hero Pediatric Anterior Carbon Fiber AFO,F3…
FDA device listing 1398271792 · Thrive Orthopedics
Key facts
| Proprietary names | F3 Anterior Carbon Fiber AFO,F3 Anterior FlexTrim Carbon Fiber AFO,F3 Hero Pediatric Anterior Carbon Fiber AFO,F3 Magnetic Anterior Carbon Fiber AFO,F3 Magnetic Anterior FlexTrim Carbon Fiber AFO,F3 Magnetic Hero Pediatric Anterior Carbon Fiber AFO,F5 Magnetic Medial Spiral Carbon Fiber AFO,F5 Magnetic Medial Spiral FlexTrim Carbon Fiber AFO,F5 Magnetic Spiral Carbon Fiber AFO,F5 Magnetic Spiral… |
|---|---|
| Owner/operator | Thrive Orthopedics |
| Owner/operator number | 10081454 |
| 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 | Thrive Orthopedics |
| Establishment registrations | 3018608552 |
| FEI numbers | 3018608552 |
| Establishment operations | Specification Developer |
| 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