Joseph M. Piocentile
Country not established
- Devices
- 1
What Joseph M. Piocentile makes
Joseph M. Piocentile manufactures transcutaneous electronic nerve stimulation (TENS) devices, which deliver low-voltage electrical currents through the skin to manage pain symptoms.
The company’s portfolio is regulated under FDA Class II devices and is listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Transcutaneous Electronic Nerve Stimu Ref K831938
510(k) 510(k)
Frequently asked questions
How many devices does Joseph M. Piocentile have in the registry?
The registry currently lists 1 device for Joseph M. Piocentile. Devices recorded under merged duplicate company entries are counted once.
Which registries list Joseph M. Piocentile's devices?
Among its 1 most recently registered device, Joseph M. Piocentile has devices listed in FDA 510(k) (1 device).
What risk classes do Joseph M. Piocentile's devices fall under?
Among its 1 most recently registered device, the classes recorded for Joseph M. Piocentile's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Joseph M. Piocentile in the registry?
The most recently registered devices listed for Joseph M. Piocentile include TRANSCUTANEOUS ELECTRONIC NERVE STIMU.