# Kvikna Ehf

- Location (FDA's records): Crofton, MD
- FDA decisions: 2 (2013–2015): 2 510(k) clearances
- Product codes: OLT (2)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medelec, Ltd.: 2 (https://510kreport.com/company/medelec)
- Natus Medical, Inc.: 1 (https://510kreport.com/company/natus-medical)
- Taugagreining HF: 1 (https://510kreport.com/company/taugagreining)

## Firms that cite its devices most
- Forest Devices, Inc.: 1 (https://510kreport.com/company/forest-devices)

## Its most-cited devices
- K143487: Lifelines iEEG (2015), cited by 1

## Recent decisions
- K143487: Lifelines iEEG (Aug 21, 2015)
- K123665: Lifelines Ieeg (Mar 25, 2013)

Source page: https://510kreport.com/company/kvikna