FDA device listing
1020 Ring Lock Hip Joint,1022 Modified Ring Lock Hip Joint,1023 Trigger Lock Hip Joint,1025 Free Motion Hip Joint,1026…
FDA device listing 2035115275 · BECKER ORTHOPEDIC APPLIANCE CO.
Key facts
| Proprietary names | 1020 Ring Lock Hip Joint,1022 Modified Ring Lock Hip Joint,1023 Trigger Lock Hip Joint,1025 Free Motion Hip Joint,1026 Adjustable Flexion Ring Lock Hip Joint,1030 Abduction Flexion Hip Joint,1040 and 1041 Millenium Hip Joint,1085 Free Motion Aluminum Thrust Bearing Hip Joint,1090 Ring Lock Aluminum Thrust Bearing Hip Joint,1095 Two Position Ring Lock Aluminum Thrust Bearing Hip Joint,1096… |
|---|---|
| Owner/operator | BECKER ORTHOPEDIC APPLIANCE CO. |
| Owner/operator number | 1824252 |
| Product codes | ITS |
| Device names | ITS - Joint, Hip, External Brace |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | BECKER ORTHOPEDIC APPLIANCE CO. |
| Establishment registrations | 1824252 |
| FEI numbers | 1000042994 |
| 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