FDA device listing
Bone Dust Trap
FDA device listing 1249171181 · RIM Medical Technologies Incorporated
Key facts
| Proprietary names | Bone Dust Trap |
|---|---|
| Owner/operator | RIM Medical Technologies Incorporated |
| Owner/operator number | 10080310 |
| Product codes | BYZ |
| Device names | BYZ - Trap, Sterile Specimen |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.6740 |
| Review panels | General Hospital |
| Registered establishments | RIM Medical Technologies Incorporated |
| Establishment registrations | 3017970304 |
| FEI numbers | 3017970304 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, 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