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Conod Medical Co., Limited

FDA Regulatory Profile

Conod Medical Co., Limited has 0 FDA recalls, 2 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 30, 2015 · VAI
Latest 510(k)
Jul 2, 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 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 30, 2015Suzhou, ChinaDevicesVoluntary Action Indicated (VAI)3005596530
May 30, 2013Suzhou, ChinaDevicesVoluntary Action Indicated (VAI)3005596530

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
K203591Single-use Medical Face MaskJul 2, 2021
K181276CONOD Enteral Feeding SetsJul 12, 2018

FDA data resources