FDA device listing
Aurix XL
FDA device listing 1082443723 · Nuo Therapeutics, Inc.
Key facts
| Proprietary names | Aurix XL |
|---|---|
| Owner/operator | Nuo Therapeutics, Inc. |
| Owner/operator number | 9058053 |
| Product codes | OFM |
| Device names | OFM - Phlebotomy Blood Collection Kit |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.2750 |
| Review panels | Cardiovascular |
| Registered establishments | NUO THERAPEUTICS, INC. |
| Establishment registrations | 3004140833 |
| FEI numbers | 3004140833 |
| Establishment operations | Specification Developer |
| 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