FDA device listing
JBA-BELT Red and Infrared Light Pain Relief Belt,JBA-FACE LLLT LED Mask Device for Face,JBA-HEAD LLLT Red and Infrared…
FDA device listing 2051824069 · AQP ONE, INC.
Key facts
| Proprietary names | JBA-BELT Red and Infrared Light Pain Relief Belt,JBA-FACE LLLT LED Mask Device for Face,JBA-HEAD LLLT Red and Infrared Light Cap,JBA-NECK LLLT LED Mask Device for Neck,JBA-PBH LLLT Pain Relief Handheld Device,JBA-PBP LLLT Pain Relief Device with 4 Pads – Therapeutic Vibrator,JBA-PSP LLLT Pain Relief Device with 2 Pads – Therapeutic Vibrator,JBA-SBH LLLT LED Skin Handheld Device,JBA-SBM LED Skin… |
|---|---|
| Owner/operator | AQP ONE, INC. |
| Owner/operator number | 10090383 |
| Product codes | ILY |
| Device names | ILY - Lamp, Infrared, Therapeutic Heating |
| Device class | Class II |
| Classification regulations (21 CFR) | 890.5500 |
| Review panels | Physical Medicine |
| Registered establishments | AQP ONE, INC. |
| Establishment registrations | 3017415521 |
| FEI numbers | 3017415521 |
| Establishment operations | Specification Developer |
| 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