# Lifescan Europe

- Location (FDA's records): Zug, CH
- FDA decisions: 3 (2015–2020): 3 510(k) clearances
- Names in FDA's records: Lifescan Europe (2); Lifescan Europe GmbH (1)
- Product codes: NBW (3)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 4 (1 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
- Cilag GmbH International: 2 (https://510kreport.com/company/cilag-international)

## Firms that cite its devices most
- Sejoy Biomedical Co., Ltd.: 1 (https://510kreport.com/company/sejoy-biomedical)
- Applied Biomedical, LLC: 1 (https://510kreport.com/company/applied-biomedical)
- Tianjin Empecs Medical Device Co., Ltd.: 1 (https://510kreport.com/company/tianjin-empecs-medical-device)

## Its most-cited devices
- K150214: OneTouch Verio Flex Blood Glucose Monitoring System (2015), cited by 3
- K193475: OneTouch Verio Reflect Blood Glucose Monitoring System (2020), cited by 1

## Recent decisions
- K193475: OneTouch Verio Reflect Blood Glucose Monitoring System (Feb 14, 2020)
- K151611: OneTouch Ultra Plus Flex Blood Glucose Monitoring System (Dec 14, 2015)
- K150214: OneTouch Verio Flex Blood Glucose Monitoring System (Jul 31, 2015)

Source page: https://510kreport.com/company/lifescan-europe