Well-Life Healthcare Limited - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Well-Life Healthcare Limited has 22 FDA 510(k) cleared neurology devices. Based in Kowloon, HK.
Latest FDA clearance: Oct 2024. Active since 2006.
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 Well-Life Healthcare Limited
22 devices
Cleared
Oct 18, 2024
Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator
Neurology
389d
Cleared
Dec 29, 2022
Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life...
Gastroenterology & Urology
129d
Cleared
Aug 04, 2022
Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)
Neurology
162d
Cleared
Feb 19, 2022
Well-Life TENS/EMS/Heating Stimulator
Neurology
148d
Cleared
Jun 01, 2021
Well-Life Garment Electrodes (GM Series)
Neurology
419d
Cleared
Oct 18, 2017
OTC Combo TENS/EMS System
Neurology
30d
Cleared
Jan 17, 2017
WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A...
Neurology
113d
Cleared
Dec 05, 2016
WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A
Neurology
193d
Cleared
Nov 14, 2014
OTC COMBO TENS/EMS SYSTEM
Neurology
179d
Cleared
Jan 28, 2014
OTC PATCH
Neurology
53d
Cleared
Jul 11, 2013
BUTTOCK MUSCLE STIMULATOR MODEL WL-2413B
Physical Medicine
283d
Cleared
Sep 07, 2012
MINI PATCH
Neurology
126d