FDA device listing
JC-600 NEO NECK STRONG,JC-612 NEO NECK DELIGHT,JC- 7007 NEO NECK PLEASURE,JC-777 NEO MULTI COLLAR
FDA device listing 1029126925 · Neomed Co., Ltd.
Key facts
| Proprietary names | JC-600 NEO NECK STRONG,JC-612 NEO NECK DELIGHT,JC- 7007 NEO NECK PLEASURE,JC-777 NEO MULTI COLLAR |
|---|---|
| Owner/operator | Neomed Co., Ltd. |
| Owner/operator number | 10053119 |
| Product codes | IQK |
| Device names | IQK - Orthosis, Cervical |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3490 |
| Review panels | Physical Medicine |
| Registered establishments | NEOMED CO., LTD. |
| Establishment registrations | 3012865799 |
| FEI numbers | 3012865799 |
| 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