Shenzhen Kentro Medical Electronics Co., Ltd. - FDA 510(k) Cleared De...
10
Total
10
Cleared
0
Denied
Shenzhen Kentro Medical Electronics Co., Ltd. has 10 FDA 510(k) cleared neurology devices. Based in Shenzhen, CN.
Latest FDA clearance: Nov 2024. Active since 2017.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Shenzhen Kentro Medical Electronics...
10 devices
Cleared
Nov 05, 2024
Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341,...
Neurology
90d
Cleared
Dec 08, 2023
Transcutaneous Electrical Nerve Stimulator For Pain Relief (Model: KTR-2302,...
Neurology
112d
Cleared
May 10, 2023
Transcutaneous Electrical Nerve Stimulator, Model: KTR-4031, KTR-4032,...
Neurology
230d
Cleared
Aug 24, 2022
Transcutaneous Electrical Nerve Stimulator, Model: KTR-405
Physical Medicine
142d
Cleared
Mar 25, 2021
Low-frequency Multi-function physiotherapy instrument
Neurology
426d
Cleared
Oct 19, 2020
Transcutaneous Electronic Nerve Stimulator
Neurology
269d
Cleared
Sep 25, 2020
Low-Frequency Multi-function Physiotherapy Instrument (Model: KTR-2230,...
Neurology
428d
Cleared
Jul 30, 2019
Transcutaneous Electrical Nerve Stimulator
Neurology
246d
Cleared
Oct 17, 2018
Muscle Trainer
Physical Medicine
110d
Cleared
May 11, 2017
Low-Frequency Therapy Instrument /Model: KTR-201, KTR-202, KTR-203
Neurology
108d