FDA device listing
ProactiveStrides,Proactive You,VSTBalance,VSTBalance Go,VSTBalance Kiosk,VSTBalance Traveller,VSTBalance Trek
FDA device listing 1745358350 · VirtuSense
Key facts
| Proprietary names | ProactiveStrides,Proactive You,VSTBalance,VSTBalance Go,VSTBalance Kiosk,VSTBalance Traveller,VSTBalance Trek |
|---|---|
| Owner/operator | VirtuSense |
| Owner/operator number | 10090399 |
| Product codes | QKC |
| Device names | QKC - Interactive Rehabilitation Exercise Device, Prescription Use |
| Device class | Class II |
| Classification regulations (21 CFR) | 890.5360 |
| Review panels | Physical Medicine |
| Registered establishments | VIRTUSENSE |
| Establishment registrations | 3023132085 |
| FEI numbers | 3023132085 |
| 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