Trekk Intl.
Country not established
- Devices
- 1
What Trekk Intl. makes
Trekk Intl. manufactures the BIOTENS, which is a transcutaneous electrical nerve stimulation device. This product is designed to provide pain relief through electrical impulses.
The device is classified as a Class II medical device and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Biotens Ref K884814
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Trekk Intl. have in the registry?
The registry currently lists 1 device for Trekk Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trekk Intl.'s devices?
Among its 1 most recently registered device, Trekk Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Trekk Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Trekk Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trekk Intl. in the registry?
The most recently registered devices listed for Trekk Intl. include BIOTENS.