FDA device listing
Lords Activeguard Back rest,Lords Activeguard Back Rest Seat Cushion,Lords Activeguard Back Support Belt,Lords…
FDA device listing 1845381199 · Lords Mark Global LLC
Key facts
| Proprietary names | Lords Activeguard Back rest,Lords Activeguard Back Rest Seat Cushion,Lords Activeguard Back Support Belt,Lords Activeguard Flexi Pore,Lords Activeguard Lumbo Back Rest,Lords Activeguard Lumbo Bcak Rest Urbane,Lords Activeguard Ortho Cushion Seat,Lords Activeguard Posture Corrector,Lords Activeguard Posture Corrector Brace,Lords Activeguard Posture Corrector Sleek |
|---|---|
| Owner/operator | Lords Mark Global LLC |
| Owner/operator number | 10093751 |
| Product codes | IQE |
| Device names | IQE - Orthosis, Lumbar |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3490 |
| Review panels | Physical Medicine |
| Registered establishments | Lords Mark Industries Ltd. |
| Establishment registrations | 3039396083 |
| FEI numbers | 3039396083 |
| 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