FDA device listing
MCP DISTAL PROGRESSIVE RASP,MCP PROXIMAL PROGRESSIVE RASP,PIP DISTAL PROGRESSIVE RASP,PIP PROXIMAL PROGRESSIVE RASP
FDA device listing 1117934791 · Keri Medical
Key facts
| Proprietary names | MCP DISTAL PROGRESSIVE RASP,MCP PROXIMAL PROGRESSIVE RASP,PIP DISTAL PROGRESSIVE RASP,PIP PROXIMAL PROGRESSIVE RASP |
|---|---|
| Owner/operator | Keri Medical |
| Owner/operator number | 10085771 |
| Product codes | GAC |
| Device names | GAC - Rasp, Surgical, General & Plastic Surgery |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | KERI MEDICAL |
| Establishment registrations | 3024706750 |
| FEI numbers | 3024706750 |
| Establishment operations | Complaint File Establishment, 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