Pain Relief Technologies
Country not established FDA establishment FEI 3018387315
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Pain Relief Technologies makes
Pain Relief Technologies manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the Electropulse series for low back pain relief and cosmetic applications. These devices deliver low-voltage electrical pulses to target pain or stimulate skin rejuvenation.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Electropulse - Low Back Pain Ref K062532
510(k) 510(k)Electropulse Ref K051128
510(k) 510(k)Electropulse-Cosmetic Ref K113724
510(k) 510(k)
Company details
- FDA FEI number
- 3018387315
- Address
- 8188 S Highland Dr., Sandy, UT, 84093
Frequently asked questions
How many devices does PAIN RELIEF TECHNOLOGIES have in the registry?
The registry currently lists 3 devices for PAIN RELIEF TECHNOLOGIES. Devices recorded under merged duplicate company entries are counted once.
Which registries list PAIN RELIEF TECHNOLOGIES's devices?
Among its 3 most recently registered devices, PAIN RELIEF TECHNOLOGIES has devices listed in FDA 510(k) (3 devices).
What risk classes do PAIN RELIEF TECHNOLOGIES's devices fall under?
Among its 3 most recently registered devices, the classes recorded for PAIN RELIEF TECHNOLOGIES's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PAIN RELIEF TECHNOLOGIES in the registry?
The most recently registered devices listed for PAIN RELIEF TECHNOLOGIES include ELECTROPULSE - LOW BACK PAIN, ELECTROPULSE and ELECTROPULSE-COSMETIC.