# Mico Biomed Co., Ltd.

- Location (FDA's records): Anseong, KR
- FDA decisions: 2 (2013–2013): 2 510(k) clearances
- Product codes: NBW (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- I-Sens, Inc.: 2 (https://510kreport.com/company/i-sens)

## Recent decisions
- K123007: Veri-Q MGD-1001 Blood Glucose Monitoring System, Veri-Q Plus MGD-1001 Blood Glucose Monitoring System (Jun 19, 2013)
- K123016: Veri-Q Self-Testing and Veri-Q Plus MGD-2001 Blood Glucose Monitoring Systems (Jun 18, 2013)

Source page: https://510kreport.com/company/mico-biomed