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Eezcare Medical Corp

FDA Regulatory Profile

Eezcare Medical Corp has 0 FDA recalls, 2 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 22, 2018 · NAI
Latest 510(k)
Feb 11, 2021

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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) clearances2Oct 4, 2026Not statedCurrent
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 22, 2018New Taipei City, TaiwanDevicesNo Action Indicated (NAI)3003801933
Dec 6, 2012New Taipei City, TaiwanDevicesNo Action Indicated (NAI)3003801933

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
K193662Ezlymph, Ezlymph MFeb 11, 2021
K191937Ezvena IPC, Ezvena SQSJan 29, 2020

FDA data resources