Relevium Labs, Inc.
Country not established
- Devices
- 2
What Relevium Labs, Inc. makes
Relevium Labs, Inc. manufactures transcutaneous neuromuscular electrical stimulation (TENS) systems designed for physical therapy applications. These devices, including the Yarlap I and Yarlap II, deliver targeted electrical stimulation to promote muscle activation and rehabilitation.
The company’s products are classified as Class II devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 080316407
- [email protected]
- Phone
- 6145687000
Frequently asked questions
How many devices does Relevium Labs, Inc. have in the registry?
The registry currently lists 2 devices for Relevium Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Relevium Labs, Inc.'s devices?
Among its 2 most recently registered devices, Relevium Labs, Inc. has devices listed in FDA GUDID (2 devices).
What risk classes do Relevium Labs, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Relevium Labs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Relevium Labs, Inc. in the registry?
The most recently registered devices listed for Relevium Labs, Inc. include Yarlap I ECS 323 and Yarlap II ECS 323P.