Jkh Health Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253150Cryon-X Cold CompressionOctober 24, 2025
K240788Ultrasound StimulatorJune 4, 2025
K240986Cold CompressionMay 1, 2024
K240011Lymphedema CompressionFebruary 23, 2024
K223541Cold/Hot CompressionOctober 27, 2023
K211050Infrared Thermometer, Model: JKH-300, JKH-301, JKH-302, JKH-303, JKH-304November 28, 2022
K202839Overlapped Compression TherapyJanuary 21, 2021
K200561StimPlus Patch, StimPlus Patch, StimPlus PatchJuly 1, 2020
K162517Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13April 14, 2017
K153520Electronic Pulse StimulatorMay 5, 2016