Nu-Beca & Maxcellent Co.
TaiwanFDA applicant, unverified
- Devices
- 1
What Nu-Beca & Maxcellent Co. makes
Nu-Beca & Maxcellent Co. manufactures transcutaneous electrical nerve stimulation (TENS) devices, designed to provide non-invasive pain relief through electrical stimulation of peripheral nerves.
Their products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nu-Beca & Maxcellent Co. have in the registry?
The registry currently lists 1 device for Nu-Beca & Maxcellent Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nu-Beca & Maxcellent Co.'s devices?
Among its 1 most recently registered device, Nu-Beca & Maxcellent Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Nu-Beca & Maxcellent Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nu-Beca & Maxcellent Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nu-Beca & Maxcellent Co. in the registry?
The most recently registered devices listed for Nu-Beca & Maxcellent Co. include Nu-beca Transcutaneous Electrical Nerve Stimulation.