FDA device listing
FM-A2701D(S),FM-A5502DC,FM-A5503DC,FM-A5504DG,FM-A5504DS,FM-A5505DGC,FM-B2702D,FM-B2702DG,FM-B2702DS,FM-C5501DG,FM-C5501…
FDA device listing 1083352667 · FORESEESON CUSTOM DISPLAYS, INC.
Key facts
| Proprietary names | FM-A2701D(S),FM-A5502DC,FM-A5503DC,FM-A5504DG,FM-A5504DS,FM-A5505DGC,FM-B2702D,FM-B2702DG,FM-B2702DS,FM-C5501DG,FM-C5501DV,FM-D5801DV,FM-D5802DV,FM-E2701D,FM-E2701DG,FM-E2701DGT,FM-E3203D,FM-E3203DC,FM-E3203DG,FM-E3204DC,FM-E3204DGC,FM-E3230D,FM-E3230DG,FM-E3230DGC,FM-E3230DN,FM-E3230DNC,FM-F2701D,FM-F2701DG,FM-F3101D,FM-F3101DG,FS-A1904D(T),FS-A2702DS,FS-A2702DST,FS-A2702DT,FS-A3202DS,FS-E2101D(T… |
|---|---|
| Owner/operator | FORESEESON CUSTOM DISPLAYS, INC. |
| Owner/operator number | 10036004 |
| Product codes | KQM |
| Device names | KQM - Camera, Surgical And Accessories |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4160 |
| Review panels | General & Plastic Surgery |
| Registered establishments | FORESEESON CUSTOM DISPLAYS, INC. |
| Establishment registrations | 3006615210 |
| FEI numbers | 3006615210 |
| Establishment operations | Complaint File Establishment, Manufacturer, Remanufacturer, 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