Everyway Medical Instruments Co.,Ltd is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Everyway Medical Instruments Co.,Ltd - FDA 510(k) Cleared Devices
Recent clearances: Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4, Everyway Analog OTC TENS, Everyway Incontinence Stimulation System
29
Total
29
Cleared
0
Denied
Everyway Medical Instruments Co.,Ltd has 29 FDA 510(k) cleared neurology devices. Based in Taipei Hsien,, TW.
Latest FDA clearance: Nov 2025. Active since 2001.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Everyway Medical Instruments Co.,Ltd
29 devices
Cleared
Nov 21, 2025
Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4
Neurology
157d
Cleared
Nov 15, 2022
Everyway Analog OTC TENS
Neurology
90d
Cleared
Dec 03, 2021
Everyway Incontinence Stimulation System
Gastroenterology & Urology
67d
Cleared
Dec 22, 2020
Everyway Analog OTC TENS, model N103A/N302
Neurology
85d
Cleared
Nov 25, 2020
Li-Battery powered OTC TENS/EMS, model EM-6000, EM-6100, EM-6200 & EM-6300
Neurology
89d
Cleared
Nov 13, 2020
Li-Battery powered OTC TENS/EMS, model EV-804, model EV-805, & model EV-806
Neurology
88d
Cleared
Oct 24, 2020
Li-Battery powered OTC TENS/EMS Combination Stimulator
Neurology
157d
Cleared
Dec 19, 2019
Everyway OTC TENS/EMS Combination
Neurology
90d
Cleared
Oct 26, 2018
A6 OTC Pain Relief TENS
Neurology
28d
Cleared
Oct 26, 2018
V2 OTC Pain Relief TENS
Neurology
28d
Cleared
Sep 26, 2018
Everyway Wireless TENS & EMS Unit
Neurology
90d
Cleared
Apr 19, 2018
EV-804 OTC Pain Relief TENS
Neurology
206d