# Icare Finland OY

- Location (FDA's records): Vantaa, FI
- FDA decisions: 7 (2016–2024): 7 510(k) clearances
- Product codes: HKY (7)
- Predicates its devices cite: 8 (5 its own); citations of its devices by later devices: 6 (5 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
- Tiolat OY: 2 (https://510kreport.com/company/tiolat)
- Golden Vision, Inc.: 1 (https://510kreport.com/company/golden-vision)

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

## Its most-cited devices
- K153694: Icare ic100 (2016), cited by 2
- K190316: Icare ic200 (2020), cited by 1
- K220852: iCare IC200 (2022), cited by 1
- K163343: Icare HOME tonometer (2017), cited by 1
- K200966: Icare HOME Tonometer (2020), cited by 1

## Recent decisions
- K241447: iCare ST500 (TA04) (Sep 27, 2024)
- K220852: iCare IC200 (Oct 6, 2022)
- K211355: iCare HOME2 (Jan 25, 2022)
- K200966: Icare HOME Tonometer (May 7, 2020)
- K190316: Icare ic200 (Jan 14, 2020)
- K163343: Icare HOME tonometer (Mar 21, 2017)
- K153694: Icare ic100 (Apr 19, 2016)

Source page: https://510kreport.com/company/icare-finland