Xuzhou Kernel Medical Equipment Co., Ltd.

FDA Regulatory Profile

Xuzhou Kernel Medical Equipment Co., Ltd. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 21, 2026.

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K261775Uv Phototherapy (KN-4001A,KN-4001B,KN-4001AB)July 21, 2026
K242977308nm Excimer Phototherapy Device (CN-308E, KN-4003B3, KN-4003B4, KN-5000C KN-5000D, KN-5000H, KN-50February 6, 2025
K222751LED Light Therapy Device, KN-7000LFebruary 1, 2023
K200971308nm Excimer SystemDecember 15, 2020
K200929Hair Growth SystemJune 3, 2020
K190685Hair Growth SystemJuly 26, 2019
K181805UV PhototherapyJanuary 11, 2019
K160341Colposcope SystemSeptember 14, 2016
K132643UV PHOTOTHERAPYJanuary 30, 2014