Curonix
United Statesfrom the FDA registration address FDA FEI 3010676138
Curonix is a medical device manufacturer, with 1 device listed in FDA 510(k) (FDA Class II) as of 12 Nov 2026.
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA 510(k) 1
- Device classes
- FDA Class II 1
- Identifiers
- FDA FEI 3010676138
At a glance
Market reach
- United States
- FDA FEI
What Curonix makes
Curonix manufactures implantable neurostimulation systems for chronic pain management, including spinal cord stimulation (SCS) and peripheral nerve stimulation (PNS) devices. Their portfolio includes pulse generators, trial neurostimulators, permanent neurostimulator receiver kits, and associated accessories. These systems are designed for long-term and temporary therapeutic electrical stimulation to alleviate pain in targeted nerve pathways.
The company’s devices are classified as Class II under FDA regulations and are authorised via the 510(k) and UDI pathways. Their products are listed in the FDA’s regulatory databases, and the company operates from the United States.
Catalogue
Freedom Peripheral Nerve Stimulator (PNS) System Ref K233162
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010676138
- Address
- 1310 Park Central Boulevard S, Pompano Beach, FL, 33064
Frequently asked questions
How many devices does Curonix have in the registry?
The registry currently lists 1 device for Curonix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curonix's devices?
Among its 1 most recently registered device, Curonix has devices listed in FDA 510(k) (1 device).
What risk classes do Curonix's devices fall under?
Among its 1 most recently registered device, the classes recorded for Curonix's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curonix in the registry?
The most recently registered devices listed for Curonix include Freedom Peripheral Nerve Stimulator (PNS) System.