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Data / Medical devices / India / Murata Vios, Private Limited

Murata Vios, Private Limited: FDA-registered device maker in Kodihalli, Bangalore Karnataka, India, 4 510(k) clearances

Murata Vios, Private Limited is registered with the FDA (registration 3015181391) in Kodihalli, Bangalore Karnataka, India. It lists 9 device types. The FDA files 4 510(k) clearances under its listings, the newest dated January 23, 2025. Registered through 2027. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3015181391
Address
Prestige Sterling Square No.204, 3rd Floor, Wing-A, 3, Madras Bank Road, Off Lavelle Road, Kodihalli, Bangalore Karnataka, India, 560001
Owner or operator
Murata Vios, Inc. (10059850)
Roles
Manufacturer, Remanufacturer, Repackager or relabeler
First device listed
February 28, 2019
Registered through
2027
Brand names listed
Vios Central Station Monitor/Vios Central Server Software 2050, Vios Monitoring System, Vios Monitoring System™ Model 2050

Devices it lists

DeviceProduct codeClassRoleSource
Detector And Alarm, ArrhythmiaDSI2Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Display, Cathode-Ray Tube, MedicalDXJ2Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Medical Device Data SystemOUG1Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)DRT2Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)MHX2Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
OximeterDQA2Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Oximeter, EarDPZ2Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
System, Measurement, Blood-Pressure, Non-InvasiveDXN2Manufacturer, Repackager or relabeleraccessdata.fda.gov
Transmitters And Receivers, Physiological Signal, RadiofrequencyDRG2Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 23, 2025K241728Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050DXNSubstantially EquivalentMurata Vios, Inc.accessdata.fda.gov
March 22, 2024K232354Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server SoftwareDRTSubstantially EquivalentMurata Vios, Inc.accessdata.fda.gov
July 26, 2018K173107Vios Central Station Monitor Software, Vios Central Server SoftwareDXJSubstantially EquivalentVios Medical, Inc.accessdata.fda.gov
June 22, 2018K172586Vios Monitoring System™ Model 2050DRTSubstantially EquivalentVios Medical, Inc.accessdata.fda.gov

Compare with other makers

Updated January 23, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.