FDA device listing
Bone Fenestration Chisel,Bone Fenestration Chisel, Curved Refresh Chisel,Straight Box Chisel 4mm x 18mm
FDA device listing 1973712973 · MedTech-LLC
Key facts
| Proprietary names | Bone Fenestration Chisel,Bone Fenestration Chisel, Curved Refresh Chisel,Straight Box Chisel 4mm x 18mm |
|---|---|
| Owner/operator | MedTech-LLC |
| Owner/operator number | 10043432 |
| Product codes | FZO |
| Device names | FZO - Chisel, Surgical, Manual |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | MEDTECH LLC |
| Establishment registrations | 3010123256 |
| FEI numbers | 3010123256 |
| Establishment operations | Contract 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