Loric Technology
Country not established
- Devices
- 1
What Loric Technology makes
Loric Technology manufactures transcutaneous electrical nerve stimulation (TENS) devices, specifically the TAD Model #9655, designed for pain management and muscle stimulation therapy.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The TENS device is listed in the FDA’s 510(k) database. Loric Technology operates from the United States.
Catalogue
Tad Model #9655 Ref K921898
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Loric Technology have in the registry?
The registry currently lists 1 device for Loric Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Loric Technology's devices?
Among its 1 most recently registered device, Loric Technology has devices listed in FDA 510(k) (1 device).
What risk classes do Loric Technology's devices fall under?
Among its 1 most recently registered device, the classes recorded for Loric Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Loric Technology in the registry?
The most recently registered devices listed for Loric Technology include TAD MODEL #9655.