Shenzhen Witleaf Medical Electronics Co., Ltd.

FDA Regulatory Profile

Shenzhen Witleaf Medical Electronics Co., Ltd. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Feb 26, 2023

Updated: recalls Oct 23, 2026 · inspections Oct 23, 2026 · compliance actions Oct 23, 2026.

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Summary

Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K213431Handheld Pulse OximeterFeb 26, 2023
K213430Fingertip Pulse OximeterDec 30, 2022