FDA device listing
Adapter footrest MBS,Additive Back support MBS,Additive Back support (viscoel.) MBS,ak 5010 MBS
FDA device listing 1623655956 · AKRUS GmbH & Co KG
Key facts
| Proprietary names | Adapter footrest MBS,Additive Back support MBS,Additive Back support (viscoel.) MBS,ak 5010 MBS |
|---|---|
| Owner/operator | AKRUS GmbH & Co KG |
| Owner/operator number | 10046166 |
| Product codes | LGX |
| Device names | LGX - Table, Examination, Medical, Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4960 |
| Review panels | General & Plastic Surgery |
| Registered establishments | AKRUS GmbH & Co. KG |
| Establishment registrations | 3006142326 |
| FEI numbers | 3006142326 |
| 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