Empi - FDA 510(k) Cleared Devices

Empi, is a historical medical device manufacturer based in Walker, US. The company specialized in electrotherapy and neurostimulation devices.

Empi received 56 FDA 510(k) clearances from 60 total submissions between 1977 and 2010. The company's primary focus was physical medicine and neurology devices, including transcutaneous nerve stimulators, iontophoresis systems, and electrotherapy equipment. This regulatory record spans over three decades of device development and market clearance.

Empi is now a historical record only, with no FDA 510(k) clearances issued in more than 13 years. The company's last cleared device was submitted in 2010. Interested parties may explore the complete list of device names, product codes, and individual clearance dates in the regulatory database.