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Shenzhen Kingyield Technology Co., Ltd.

FDA Regulatory Profile

Shenzhen Kingyield Technology Co., Ltd. has 0 FDA recalls, 2 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest inspection
Mar 5, 2015 · NAI
Latest 510(k)
Oct 6, 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) clearances5Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 5, 2015Shenzhen China, ChinaDevicesNo Action Indicated (NAI)3007420856
May 4, 2012Shenzhen China, ChinaDevicesVoluntary Action Indicated (VAI)3007420856

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
K182018Bluetooth blood pressure monitorOct 6, 2018
K161530Bluetooth blood pressure monitorMar 31, 2017
K123801FINGER PULSE OXIMETERMay 28, 2013
K112042KINGYIELD WRIST BLOOD PRESSURE MONITORFeb 10, 2012
K083043KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201Oct 27, 2008

FDA data resources