FDA device listing
07-829-11 Rotatable Biopsy Forceps, 2mm Spoon, 12cm WL,07-829-12 Rotatable Biopsy Forceps, 2mm Spoon, 15cm WL,07-829-13…
FDA device listing 1713630383 · MIZUHO AMERICA, INC.
Key facts
| Proprietary names | 07-829-11 Rotatable Biopsy Forceps, 2mm Spoon, 12cm WL,07-829-12 Rotatable Biopsy Forceps, 2mm Spoon, 15cm WL,07-829-13 Rotatable Biopsy Forceps, 45 Degrees Up, 2mm Spoon, 12cm WL,07-829-14 Rotatable Biopsy Forceps, 45 Degrees Up, 2mm Spoon, 15cm WL,07-829-15 Rotatable Biopsy Forceps, 45 Degrees Up, 2x5mm Spoon, 12cm WL,07-829-16 Rotatable Biopsy Forceps, 45 Degrees Up, 2x5mm Spoon, 15cm… |
|---|---|
| Owner/operator | MIZUHO AMERICA, INC. |
| Owner/operator number | 9008103 |
| Product codes | HTD |
| Device names | HTD - Forceps |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | MIZUHO AMERICA, INC. |
| Establishment registrations | 1223656 |
| FEI numbers | 1000159388 |
| Establishment operations | Manufacturer, Repackager/Relabeler, 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