Pain Management Technologies
Country not established FDA establishment FEI 1000122747
- Devices
- 20
- Registrations
- FDA
- FDA recalls
- 0
What Pain Management Technologies makes
Pain Management Technologies manufactures transcutaneous electrical nerve stimulation (TENS) devices and accessories, including self-adhesive electrodes, soft-touch TENS electrodes, and joint stimulation units like the Joint Stim Model 1000. Their product line also includes rechargeable TENS units such as the Ultima Neo and Ultima Five, designed for pain relief applications.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company’s portfolio is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Search and filter all 20 devicesCompany details
- FDA FEI number
- 1000122747
- Address
- 1760 Wadsworth Rd, AKRON, OH, 44320
Frequently asked questions
How many devices does PAIN MANAGEMENT TECHNOLOGIES have in the registry?
The registry currently lists 20 devices for PAIN MANAGEMENT TECHNOLOGIES. Devices recorded under merged duplicate company entries are counted once.
Which registries list PAIN MANAGEMENT TECHNOLOGIES's devices?
Among its 20 most recently registered devices, PAIN MANAGEMENT TECHNOLOGIES has devices listed in FDA 510(k) (6 devices) and FDA GUDID (14 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PAIN MANAGEMENT TECHNOLOGIES's devices fall under?
Among its 20 most recently registered devices, the classes recorded for PAIN MANAGEMENT TECHNOLOGIES's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PAIN MANAGEMENT TECHNOLOGIES in the registry?
The most recently registered devices listed for PAIN MANAGEMENT TECHNOLOGIES include iTENS Large gel pads, iTENS Small gel pads, iTENS Long gel pads and Pain Management Technologies Ultima 5.