# Innokas Yhtyma

- Location (FDA's records): Kempele, Oulu, FI
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: MWI (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ge Medical Systems Information Technologies: 1 (https://510kreport.com/company/ge-medical-systems-information-technologies)
- Welch Allyn, Inc.: 1 (https://510kreport.com/company/welch-allyn)
- Masimo Corporation: 1 (https://510kreport.com/company/masimo)
- Covidien: 1 (https://510kreport.com/company/covidien)

## Firms that cite its devices most
- Ge Medical Systems Information Technologies: 2 (https://510kreport.com/company/ge-medical-systems-information-technologies)

## Its most-cited devices
- K133810: VC150 Vital Signs Monitor (2014), cited by 2

## Recent decisions
- K133810: VC150 Vital Signs Monitor (Oct 30, 2014)

Source page: https://510kreport.com/company/innokas-yhtyma