Visiomed AG
Country not established
- Devices
- 1
What Visiomed AG makes
Visiomed AG manufactures Microderm Model/Version 3.5, a Class II medical device designed for dermatological treatments, including skin resurfacing and exfoliation procedures.
The device is regulated under FDA 510(k) clearance as a Class II product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Microderm, Model/Version 3.5 Ref K040171
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Visiomed AG have in the registry?
The registry currently lists 1 device for Visiomed AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visiomed AG's devices?
Among its 1 most recently registered device, Visiomed AG has devices listed in FDA 510(k) (1 device).
What risk classes do Visiomed AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Visiomed AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Visiomed AG in the registry?
The most recently registered devices listed for Visiomed AG include MICRODERM, MODEL/VERSION 3.5.