Koya, Inc.
Country not established
- Devices
- 1
What Koya, Inc. makes
Koya, Inc. manufactures the Koya Ripple, a medical device designed for use in cardiac electrophysiology procedures, specifically for mapping and ablation of cardiac arrhythmias.
The Koya Ripple is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Koya Ripple Ref K193288
510(k) 510(k)
Frequently asked questions
How many devices does Koya, Inc. have in the registry?
The registry currently lists 1 device for Koya, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Koya, Inc.'s devices?
Among its 1 most recently registered device, Koya, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Koya, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Koya, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Koya, Inc. in the registry?
The most recently registered devices listed for Koya, Inc. include Koya Ripple.