ClearanceBrief
Company ยท CN

Shenzhen Konmed Technology Co., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2026. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KPIStimulator, Electrical, Non-Implantable, For Incontinence4
GXYElectrode, Cutaneous2
IPFStimulator, Muscle, Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 18, 2026K260178Pelvic Muscle Trainer (KM510, KM516B)
Shenzhen Konmed Technology Co., Ltd., CN
KPI
Feb 23, 2024K233576Konmed Incontinence Stimulation Electrode (Vaginal Probe: KM-503, KM-504, KM-505, KM-506, KM-507, KM-5013; Rectal Probe:
Shenzhen Konmed Technology Co., Ltd., CN
KPI
Jul 20, 2022K220161Biofeedback Nerve and Muscle Stimulator
Shenzhen Konmed Technology Co., Ltd., CN
KPI
Dec 8, 2020K202648Biofeedback Nerve and Muscle Stimulator
Shenzhen Konmed Technology Co., Ltd., CN
IPF
Jan 18, 2018K163288Pelvifine Pelvic Muscle Trainer
Shenzhen Konmed Technology Co., Ltd., CN
KPI
Jan 10, 2018K171722Electrodes with snap / Electrodes with pigtail
Shenzhen Konmed Technology Co., Ltd., CN
GXY
Jan 5, 2018K171721Electrodes with silver conductive
Shenzhen Konmed Technology Co., Ltd., CN
GXY

Latest recalls

DateFirm and productCodeLinked 510(k)
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