Kvikna Ehf
Country not established
- Devices
- 2
What Kvikna Ehf makes
Kvikna Ehf manufactures intracranial electroencephalography (iEEG) systems, specifically the Lifelines iEEG devices, designed for continuous monitoring of brain electrical activity in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Lifelines iEEG Ref K143487
510(k) 510(k)Lifelines Ieeg Ref K123665
510(k) 510(k)
Frequently asked questions
How many devices does Kvikna Ehf have in the registry?
The registry currently lists 2 devices for Kvikna Ehf. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kvikna Ehf's devices?
Among its 2 most recently registered devices, Kvikna Ehf has devices listed in FDA 510(k) (2 devices).
What risk classes do Kvikna Ehf's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kvikna Ehf's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kvikna Ehf in the registry?
The most recently registered devices listed for Kvikna Ehf include Lifelines iEEG.