# Cilag GmbH International

- Location (FDA's records): Zug, CH
- FDA decisions: 3 (2011–2013): 3 510(k) clearances
- Product codes: NBW (2), LFR (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Lifescan, Inc.: 2 (https://510kreport.com/company/lifescan)

## Firms that cite its devices most
- Lifescan Europe: 2 (https://510kreport.com/company/lifescan-europe)

## Its most-cited devices
- K131363: Onetouch Verio Blood Glucose Monitoring System (2013), cited by 2
- K110637: Onetouch Verio (TM) IQ Blood Glucose Monitoring System (2011), cited by 1

## Recent decisions
- K131363: Onetouch Verio Blood Glucose Monitoring System (Aug 30, 2013)
- K120708: Onetouch Verio Sync Blood Glucose Monitoring System (Feb 7, 2013)
- K110637: Onetouch Verio (TM) IQ Blood Glucose Monitoring System (Sep 7, 2011)

Source page: https://510kreport.com/company/cilag-international