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Televere Systems

FDA Regulatory Profile

Televere Systems has 0 FDA recalls, 2 inspections, 6 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 22, 2026 · VAI
Latest 510(k)
Jun 20, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances6Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 22, 2026Janesville, WIDevicesVoluntary Action Indicated (VAI)3002906551
Nov 29, 2018Janesville, WIDevicesNo Action Indicated (NAI)3002906551

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K181358Televere Digital Dental Imaging SystemJun 20, 2018
K180765Televere Podiatry X-Ray System HFApr 20, 2018
K172124Televere Podiatry Digital Imaging SystemNov 9, 2017
K170975Televere Digital Imaging SystemMay 1, 2017
K082623VISIX IMAGINGFeb 25, 2009
K061035TIGERVIEW PROFESSIONALJun 5, 2006

FDA data resources