FDA device listing
Joint, Knee, External Brace
FDA device listing 1041424327 · VARC, Inc.
Key facts
| Owner/operator | VARC, Inc. |
|---|---|
| Owner/operator number | 10046941 |
| 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 | VALLEY PACKAGING INDUSTRIES, INC., Vernon Area Rehabilitation Center, Inc. - Juneau Division, Vernon Area Rehabilitation Center, Inc. - La Crosse Division, Vernon Area Rehabilitation Center, Inc. - Richland Division, Vernon Area Rehabilitation Center, Inc. - Sauk Division, Vernon Area Rehabilitation Center, Inc. - Viroqua Division |
| Establishment registrations | 3006789548, 3010872396, 3010951382, 3010951384, 3010952189, 3015337116 |
| FEI numbers | 3006789548, 3010872396, 3010951382, 3010951384, 3010952189, 3015337116 |
| Establishment operations | 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