FDA device listing
Bare Fiber 400 T Luer Lock,Bare Fiber 600 T Luer Lock,CORONA 360 Fused 600 1.8 US,CORONA Infinite Ring XSCF 600 1.6…
FDA device listing 1934632752 · Osmunds
Key facts
| Proprietary names | Bare Fiber 400 T Luer Lock,Bare Fiber 600 T Luer Lock,CORONA 360 Fused 600 1.8 US,CORONA Infinite Ring XSCF 600 1.6 US,Rigid Infinite Ring HSC Probe 600 1.8 US |
|---|---|
| Owner/operator | Osmunds |
| Owner/operator number | 10056745 |
| Product codes | GEX |
| Device names | GEX - Powered Laser Surgical Instrument |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4810 |
| Review panels | General & Plastic Surgery |
| Registered establishments | OSMUNDS |
| Establishment registrations | 3016445722 |
| FEI numbers | 3016445722 |
| Establishment operations | Contract Sterilizer |
| 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