FDA device listing
Stern Podia Exam Chair
FDA device listing 1893839394 · ATLAS INTL.
Key facts
| Proprietary names | Stern Podia Exam Chair |
|---|---|
| Owner/operator | ATLAS INTL. |
| Owner/operator number | 9007577 |
| Product codes | FRK |
| Device names | FRK - Chair, Examination And Treatment |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6140 |
| Review panels | General Hospital |
| Registered establishments | ATLAS INTL. |
| Establishment registrations | 2951225 |
| FEI numbers | 1000221494 |
| Establishment operations | Repackager/Relabeler |
| 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