FDA device listing
Aladuck2 V100,Aladuck2 V220,Aladuck405 V100,Aladuck405 V220
FDA device listing 1660158120 · ARS Co., Ltd.
Key facts
| Proprietary names | Aladuck2 V100,Aladuck2 V220,Aladuck405 V100,Aladuck405 V220 |
|---|---|
| Owner/operator | ARS Co., Ltd. |
| Owner/operator number | 10087512 |
| Product codes | NTN |
| Device names | NTN - Led Light Source |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | ARS CO., LTD. |
| Establishment registrations | 3019512034 |
| FEI numbers | 3019512034 |
| 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