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Shenzhen Mericonn Technology Co., Ltd.

FDA Regulatory Profile

Shenzhen Mericonn Technology Co., Ltd. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 18, 2026.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K254171Mesh Nebulizer (UN204); Mesh Nebulizer (UN205); Mesh Nebulizer (UN209); Mesh Nebulizer (UN210)September 18, 2026
K212300Pulse OximeterFebruary 25, 2022
K212084Fetal DopplerNovember 3, 2021

FDA data resources