Equipmed North America, Inc.
Country not established
- Devices
- 1
What Equipmed North America, Inc. makes
Equipmed North America, Inc. manufactures the ELUX 810 LASER, a medical device designed for specific dermatological or cosmetic treatments using laser technology.
The ELUX 810 LASER is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Elux 810 Laser Ref K141986
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Equipmed North America, Inc. have in the registry?
The registry currently lists 1 device for Equipmed North America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Equipmed North America, Inc.'s devices?
Among its 1 most recently registered device, Equipmed North America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Equipmed North America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Equipmed North America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Equipmed North America, Inc. in the registry?
The most recently registered devices listed for Equipmed North America, Inc. include ELUX 810 LASER.