FDA device listing
ARX Swabs: Nasopharyngeal & Tapered Tip 100 & 80mm breakpoint; Oropharyngeal 100 & 80 & 30mm breakpoint;Anterior Nares
FDA device listing 1022195420 · ARX Sciences
Key facts
| Proprietary names | ARX Swabs: Nasopharyngeal & Tapered Tip 100 & 80mm breakpoint; Oropharyngeal 100 & 80 & 30mm breakpoint ;Anterior Nares |
|---|---|
| Owner/operator | ARX Sciences |
| Owner/operator number | 10063137 |
| Product codes | KXG |
| Device names | KXG - Applicator, Absorbent Tipped, Sterile |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6025 |
| Review panels | General Hospital |
| Registered establishments | ARX SCIENCES |
| Establishment registrations | 3016587486 |
| FEI numbers | 3016587486 |
| Establishment operations | 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