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Bioland Technology, Ltd.

FDA Regulatory Profile

Bioland Technology, Ltd. has 0 FDA recalls, 1 inspection, 8 510(k) clearances and 1 compliance action on record.

Latest inspection
Mar 20, 2014 · OAI
Latest 510(k)
Aug 12, 2022

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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) clearances8Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions1Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 20, 2014Shenzhen, ChinaDevicesOfficial Action Indicated (OAI)3004101980

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
K202739Bioland G-425-2V Blood Glucose Monitoring System, Bioland G-425-2 Blood Glucose Monitoring SystemAug 12, 2022
K213011Infrared Thermometer (model: E201)Apr 5, 2022
K201879Digital Thermometer Model T103, T104Mar 31, 2021
K202934Blood Pressure MonitorJan 26, 2021
K201161Infrared Thermometer Model E127Oct 2, 2020
K201467Blood Pressure Monitor-Model 2005, 2006-2, 2006-2BSep 21, 2020
K191657Bioland Blood Glucose Monitoring SystemMar 20, 2020
K083681BIOLAND BLOOD PRESSURE MONITORJan 16, 2009

FDA data resources