Shenzhen Konmed Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Konmed Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Konmed Incontinence Stimulation Electrode (Vaginal Probe: KM-503, KM-504, KM-505, KM-506, KM-507, KM-5013, Biofeedback Nerve and Muscle Stimulator, Biofeedback Nerve and Muscle Stimulator
7
Total
7
Cleared
0
Denied
Shenzhen Konmed Technology Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Jun 2026. Active since 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Konmed Technology Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Guangzhou GLOMED Biological Technology Co., Ltd., Feiying Drug & Medical Consulting Technical Service Group and Guangzhou Glomed Biological Technoloy Co., Ltd..
FDA 510(k) Regulatory Record - Shenzhen Konmed Technology Co., Ltd.
7 devices
Cleared
Jun 18, 2026
Pelvic Muscle Trainer (KM510, KM516B)
Gastroenterology & Urology
148d
Cleared
Feb 23, 2024
Konmed Incontinence Stimulation Electrode (Vaginal Probe: KM-503, KM-504,...
Gastroenterology & Urology
108d
Cleared
Jul 20, 2022
Biofeedback Nerve and Muscle Stimulator
Gastroenterology & Urology
181d
Cleared
Dec 08, 2020
Biofeedback Nerve and Muscle Stimulator
Physical Medicine
88d
Cleared
Jan 18, 2018
Pelvifine Pelvic Muscle Trainer
Gastroenterology & Urology
422d
Cleared
Jan 10, 2018
Electrodes with snap / Electrodes with pigtail
Neurology
212d
Cleared
Jan 05, 2018
Electrodes with silver conductive
Neurology
207d