Lightray-Plus Ltd
Country not established
- Devices
- 2
What Lightray-Plus Ltd makes
LightRay-Plus Ltd manufactures transcutaneous neuromuscular electrical stimulation (TENS) systems designed for physical therapy applications. These devices are intended to deliver targeted electrical stimulation to promote muscle activation and nerve modulation for therapeutic purposes.
The company’s portfolio is classified under Class II devices and is 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
- 521166280
Frequently asked questions
How many devices does LIGHTRAY-PLUS LTD have in the registry?
The registry currently lists 2 devices for LIGHTRAY-PLUS LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list LIGHTRAY-PLUS LTD's devices?
Among its 2 most recently registered devices, LIGHTRAY-PLUS LTD has devices listed in FDA GUDID (2 devices).
What risk classes do LIGHTRAY-PLUS LTD's devices fall under?
Among its 2 most recently registered devices, the classes recorded for LIGHTRAY-PLUS LTD's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LIGHTRAY-PLUS LTD in the registry?
The most recently registered devices listed for LIGHTRAY-PLUS LTD include NeMa-st - soleve 3.3 and NeMa-st - soleve 3.2.