Transamerica Medical Systems
Country not established
- Devices
- 3
What Transamerica Medical Systems makes
Transamerica Medical Systems manufactures electrotherapy devices, including reusable electrodes for electrical stimulation and digital electrotherapy units. Their portfolio also includes transcutaneous electrical nerve stimulation (TENS) units designed for pain management applications.
These devices are classified as Class II under US regulations and are listed via the FDA’s 510(k) pathway. The company operates from the United States.
Catalogue
Transamerica Electrode Ref K961749
Regimes: 510(k) Registry: 510(k)Transamerica Digital Ems Ref K010665
Regimes: 510(k) Registry: 510(k)Transamerican Tens Ref K010782
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transamerica Medical Systems have in the registry?
The registry currently lists 3 devices for Transamerica Medical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transamerica Medical Systems's devices?
Among its 3 most recently registered devices, Transamerica Medical Systems has devices listed in FDA 510(k) (3 devices).
What risk classes do Transamerica Medical Systems's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Transamerica Medical Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transamerica Medical Systems in the registry?
The most recently registered devices listed for Transamerica Medical Systems include TRANSAMERICA ELECTRODE, TRANSAMERICA DIGITAL EMS and TRANSAMERICAN TENS.