Umeheal, Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Umeheal, Ltd. makes
Umeheal, Ltd. manufactures the RelieforMe TENS/EMS Device (Model UPK-GE01), a transcutaneous electrical nerve stimulation (TENS) and electrical muscle stimulation (EMS) device designed for pain management and muscle stimulation.
The company’s portfolio is regulated under Class II devices in the U.S. and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
RelieforMe TENS/EMS Device Model UPK-GE01 Ref K192733
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Umeheal, Ltd. have in the registry?
The registry currently lists 1 device for Umeheal, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Umeheal, Ltd.'s devices?
Among its 1 most recently registered device, Umeheal, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Umeheal, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Umeheal, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Umeheal, Ltd. in the registry?
The most recently registered devices listed for Umeheal, Ltd. include RelieforMe TENS/EMS Device Model UPK-GE01.