Jane I. Kundin
Country not established
- Devices
- 1
What Jane I. Kundin makes
Jane I. Kundin manufactures the Kundin Wound Gauge, a device designed for measuring wound dimensions to aid in clinical assessment and treatment planning.
The Kundin Wound Gauge is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Kundin Wound Gauge Ref K863409
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jane I. Kundin have in the registry?
The registry currently lists 1 device for Jane I. Kundin. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jane I. Kundin's devices?
Among its 1 most recently registered device, Jane I. Kundin has devices listed in FDA 510(k) (1 device).
What risk classes do Jane I. Kundin's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jane I. Kundin's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jane I. Kundin in the registry?
The most recently registered devices listed for Jane I. Kundin include KUNDIN WOUND GAUGE.