FDA device listing
saline nasal spray 15ml,30ml,50ml,60ml,70ml,80ml,100ml,120ml,150ml,200ml
FDA device listing 1515363514 · Chengdu Lanrun Biotechnology Co.,Ltd
Key facts
| Proprietary names | saline nasal spray 15ml,30ml,50ml,60ml,70ml,80ml,100ml,120ml,150ml,200ml |
|---|---|
| Owner/operator | Chengdu Lanrun Biotechnology Co.,Ltd |
| Owner/operator number | 10094854 |
| Product codes | KCO |
| Device names | KCO - Nasal Spray, Ent Delivery |
| Device class | Class I |
| Classification regulations (21 CFR) | 874.5220 |
| Review panels | Ear, Nose, & Throat |
| Registered establishments | CHENGDU LANRUN BIOTECHNOLOGY CO.,LTD |
| Establishment registrations | 3043149283 |
| FEI numbers | 3043149283 |
| Establishment operations | Foreign Exporter, 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