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Data / Medical devices / United States / Televere Systems

Televere Systems: FDA-registered device maker in Janesville, WI, United States, 2 510(k) clearances

Televere Systems is registered with the FDA (registration 2954358) in Janesville, WI, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated February 25, 2009. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2954358
FEI number
3002906551
Address
2302 Beloit Avenue, Janesville, WI, United States, 53546
Owner or operator
TELEVERE SYSTEMS (9040084)
Roles
Contract manufacturer, Manufacturer
First device listed
December 19, 2006
Registered through
2026
Brand names listed
ExamVue PACS, OpenImage, TIGERVIEW PROFESSIONAL, Visix Imaging, Visix for Polaris

Devices it lists

DeviceProduct codeClassRoleSource
System, Image Processing, RadiologicalLLZ2Contract manufacturer, Manufactureraccessdata.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
February 25, 2009K082623VISIX IMAGINGLLZSubstantially EquivalentTelevere Systemsaccessdata.fda.gov
June 5, 2006K061035TIGERVIEW PROFESSIONALLLZSubstantially EquivalentTelevere Systemsaccessdata.fda.gov

Compare with other makers

Updated February 25, 2009. 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.