Kundt + Co. AG
Country not established
- Devices
- 1
What Kundt + Co. AG makes
Kundt + Co. AG manufactures medical support stockings, specifically the VenoFit Lastoflex product.
The device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Med. Support Stocking-Venofit Lastoflex Ref K842708
510(k) 510(k)
Frequently asked questions
How many devices does Kundt + Co. AG have in the registry?
The registry currently lists 1 device for Kundt + Co. AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kundt + Co. AG's devices?
Among its 1 most recently registered device, Kundt + Co. AG has devices listed in FDA 510(k) (1 device).
What risk classes do Kundt + Co. AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kundt + Co. AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kundt + Co. AG in the registry?
The most recently registered devices listed for Kundt + Co. AG include MED. SUPPORT STOCKING-VENOFIT LASTOFLEX.