Comtek Intl., Corp.
Country not established
- Devices
- 1
What Comtek Intl., Corp. makes
Comtek Intl. Corp. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the EXTRA TENS (RI-2500) and NEO TENS (RI-2000E), designed for pain management through electrical stimulation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Extra Tens (Ri-2500) Neo Tens (Ri-2000E) Ref K963507
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Comtek Intl., Corp. have in the registry?
The registry currently lists 1 device for Comtek Intl., Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Comtek Intl., Corp.'s devices?
Among its 1 most recently registered device, Comtek Intl., Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Comtek Intl., Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Comtek Intl., Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Comtek Intl., Corp. in the registry?
The most recently registered devices listed for Comtek Intl., Corp. include EXTRA TENS (RI-2500) NEO TENS (RI-2000E).