FDA device listing
FF PRO WRIST
FDA device listing 1394643892 · Zhejiang Steriger Sports Medicine Technology Co.,Ltd
Key facts
| Proprietary names | FF PRO WRIST |
|---|---|
| Owner/operator | Zhejiang Steriger Sports Medicine Technology Co.,Ltd |
| Owner/operator number | 10051882 |
| Product codes | ILH |
| Device names | ILH - Splint, Hand, And Components |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | Zhejiang Steriger Sports Medicine Technology Co.,Ltd |
| Establishment registrations | 3012951155 |
| FEI numbers | 3012951155 |
| Establishment operations | Contract Manufacturer, Foreign Exporter, 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