Shenzhen Yuezhongxing Technology Co., Ltd.

FDA Regulatory Profile

Shenzhen Yuezhongxing Technology Co., Ltd. appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent FDA inspection ended on Jul 31, 2025 (Official Action Indicated (OAI)). Its most recent 510(k) clearance was granted on Mar 15, 2024.

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Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Known Names

Shenzhen Yuezhongxing Technology Co, Shenzhen Yuezhongxing Technology

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 31, 2025Huizhou, ChinaDevicesOfficial Action Indicated (OAI)3017207990

FDA Data Dashboard classifications: NAI (no action indicated), VAI (voluntary action indicated), OAI (official action indicated).

Recent 510(k) Clearances

K-NumberDeviceDate
K233799Wrist Blood Pressure Monitor (222); Wrist Blood Pressure Monitor (222BT); Wrist Blood Pressure…Mar 15, 2024
K222926Arm Blood Pressure Monitor, Model Name:111, Arm Blood Pressure Monitor, Model Name: B1681, Arm Blood…May 5, 2023
K211041Wrist Blood Pressure Monitor, Model Name:W203, Wrist Blood Pressure Monitor, Model Name:W202, Wrist…Aug 30, 2021