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Dongguan Mars Medical Products Co., Ltd.

FDA Regulatory Profile

Dongguan Mars Medical Products Co., Ltd. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Jun 16, 2016 · NAI
Latest 510(k)
Jun 18, 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 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 16, 2016Shatian, ChinaDevicesNo Action Indicated (NAI)3003171455
May 30, 2013Shatian, ChinaDevicesNo Action Indicated (NAI)3003171455

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
K191209Aneroid Type Blood Pressure KitJun 18, 2019

FDA data resources