FDA device listing
NeckCare Exercises,NeckCare Home
FDA device listing 1334576086 · NeckCare Holding
Key facts
| Proprietary names | NeckCare Exercises,NeckCare Home |
|---|---|
| Owner/operator | NeckCare Holding |
| Owner/operator number | 10084645 |
| 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 | NECKCARE, NeckCare Enterprises, Inc |
| Establishment registrations | 3022115591, 3034089185 |
| FEI numbers | 3022115591, 3034089185 |
| Establishment operations | Complaint File Establishment, Contract Manufacturer, 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