MAUDE manufacturer profile
CURONIX LLC · GZF
MAUDE profile for Stimulator, Peripheral Nerve, Implanted (Pain Relief)
Key facts
| Manufacturer | CURONIX LLC |
|---|---|
| Manufacturer group | CURONIX LLC |
| Product code | GZF |
| Product code name | Stimulator, Peripheral Nerve, Implanted (Pain Relief) |
At a glance
- 100–999 MAUDE reports
- 1–9 Death reports
- 100–999 Injury reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Use of Device Problem, Pain, Skin Infection, Impaired Healing, Erosion, Post Operative Wound Infection, Electric Shock Most reported problems
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE manufacturer and product code profiles
Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.
Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1