FDA device listing
ZK-Motion KNEE 2XL,ZK-Motion KNEE 3XL,ZK-Motion KNEE L,ZK-Motion KNEE M,ZK-Motion KNEE S,ZK-Motion KNEE XL
FDA device listing 1730354629 · D-M CHAIN COOPERATIVE
Key facts
| Proprietary names | ZK-Motion KNEE 2XL,ZK-Motion KNEE 3XL,ZK-Motion KNEE L,ZK-Motion KNEE M,ZK-Motion KNEE S,ZK-Motion KNEE XL |
|---|---|
| Owner/operator | D-M CHAIN COOPERATIVE |
| Owner/operator number | 10046809 |
| Product codes | ITQ |
| Device names | ITQ - Joint, Knee, External Brace |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | D-M CHAIN COOPERATIVE |
| Establishment registrations | 3010880695 |
| FEI numbers | 3010880695 |
| Establishment operations | Contract 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