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ALLEVA MEDICAL (D.G.) LTD

FDA Regulatory Profile

ALLEVA MEDICAL (D.G.) LTD has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Nov 6, 2025 · NAI
Latest 510(k)
Aug 27, 2019

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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) clearances1Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 6, 2025Dong Guan, ChinaDevicesNo Action Indicated (NAI)3010308146
Jun 22, 2016Dong Guan, ChinaDevicesNo Action Indicated (NAI)3010308146

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
K191107PlexusAug 27, 2019

FDA data resources