Transamerica Biomedical, Inc.
Country not established
- Devices
- 1
What Transamerica Biomedical, Inc. makes
Transamerica Biomedical, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the Transamerican Classic TENS unit, designed for pain management through low-voltage electrical currents.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance in the United States. The manufacturer operates from the US.
Catalogue
Transamerican Classic Tens Ref K944280
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transamerica Biomedical, Inc. have in the registry?
The registry currently lists 1 device for Transamerica Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transamerica Biomedical, Inc.'s devices?
Among its 1 most recently registered device, Transamerica Biomedical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Transamerica Biomedical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Transamerica Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transamerica Biomedical, Inc. in the registry?
The most recently registered devices listed for Transamerica Biomedical, Inc. include TRANSAMERICAN CLASSIC TENS.