Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Murata ManufacturingLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Murata Vios with 4 device recalls and 2 510(k) clearances. The most recent is a 510(k) clearance dated Jan 23, 2025: Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server ….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 23, 2025 | Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050K241728 · DXN | 510(k) clearances |
| Aug 9, 2024 | Vios Monitoring System Bedside Monitor Model BSM2050Class II · Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted | Device recalls |
| Apr 22, 2024 | muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rateClass II · During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms | Device recalls |
| Mar 22, 2024 | Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server SoftwareK232354 · DRT | 510(k) clearances |
| Jun 6, 2023 | Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00Class II · A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios | Device recalls |
| Jun 21, 2021 | muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rateClass II · During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
