FDA device listing
PureLift Pro Plus
FDA device listing 1555281134 · XTREEM PULSE
Key facts
| Proprietary names | PureLift Pro Plus |
|---|---|
| Owner/operator | XTREEM PULSE |
| Owner/operator number | 10057865 |
| Premarket submissions | K221443 |
| Product codes | NFO |
| Device names | NFO - Stimulator, Transcutaneous Electrical, Aesthetic Purposes |
| Device class | Class II |
| Classification regulations (21 CFR) | 882.5890 |
| Review panels | Neurology |
| Registered establishments | XTREEM PULSE |
| Establishment registrations | 3012470925 |
| FEI numbers | 3012470925 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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