Europro, Inc.
Country not established
- Devices
- 1
What Europro, Inc. makes
Europro, Inc. manufactures the DEALIGHT IPL, a device designed for intense pulsed light therapy applications.
The DEALIGHT IPL is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Dealight Ipl Ref K043032
510(k) 510(k)
Frequently asked questions
How many devices does Europro, Inc. have in the registry?
The registry currently lists 1 device for Europro, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Europro, Inc.'s devices?
Among its 1 most recently registered device, Europro, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Europro, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Europro, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Europro, Inc. in the registry?
The most recently registered devices listed for Europro, Inc. include DEALIGHT IPL.