FDA device listing
OneTouch Verio Reflect Blood Glucose Monitoring System
FDA device listing 1088836505 · Lifescan Scotland Ltd.
Key facts
| Proprietary names | OneTouch Verio Reflect Blood Glucose Monitoring System |
|---|---|
| Owner/operator | Lifescan Scotland Ltd. |
| Owner/operator number | 9026104 |
| Product codes | NBW |
| Device names | NBW - System, Test, Blood Glucose, Over The Counter |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1345 |
| Review panels | Clinical Chemistry |
| Registered establishments | LIFESCAN SCOTLAND LTD |
| Establishment registrations | 3001058982 |
| FEI numbers | 3001058982 |
| Establishment operations | Contract 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