Kvikna Medical Ehf

FDA Filings

This page includes the latest FDA filings for Kvikna Medical Ehf. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3011047165
FEI Number3011047165
NameConor Butts
Owner & OperatorKvikna Medical ehf
Contact AddressLynghals 9
Reykjavik IS-0 Reykjavik 110 IS
Official Correspondent
  • Gardar Thorvardsson
  • 354-578-8400-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4545 Fuller Drive
Irving, TX 75038 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Kvikna Medical ehf.
Stratus EEG 2021-02-05
Kvikna Medical ehf.
Stratus EEG 2021-02-05
Kvikna Medical ehf.
Stratus EEG 2021-02-05
Kvikna Medical ehf.
Stratus EEG 2020-09-09
Kvikna Medical ehf.
Lifelines iEEG 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Clinical Desktop System 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Portable Yoga Tablet No Video 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Server Software 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Client Software 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Portable Laptop System No Video 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Portable Laptop System Wireless 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Portable Laptop System Wired 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Portable Yoga Tablet Wireless 2018-07-06
Kvikna Medical ehf.
Lifelines iEEG Portable Yoga Tablet Wired 2018-07-06
Conor Butts [Kvikna Medical ehf]
Lifelines iEEG2016-09-06
Conor Butts [Kvikna Medical ehf]
Lifelines iEEG2016-04-04
Conor Butts [Kvikna Medical ehf]
Lifelines iEEG2016-04-04

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