Murata Vios, Inc.
Murata Vios, Inc. holds FDA 510(k) medical device clearances, first cleared 2024, most recent 2025, with 4 FDA device recalls on record.
Top product codes for Murata Vios, Inc.
FDA recalls by Murata Vios, Inc.
- Z-1292-2025 — Vios Monitoring System Bedside Monitor Model BSM2050
- Z-1069-2025 — muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
- Z-1169-2025 — Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00
- Z-0956-2025 — muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Murata Vios, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.