Everyway Medical Instruments Co.,Ltd FDA Approvals

0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4510(k)Nov 21, 2025Neurology	Neurology	510(k)Substantially Equivalent (Special)	Nov 21, 2025
Everyway Analog OTC TENS510(k)Nov 15, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Nov 15, 2022
Everyway Incontinence Stimulation System510(k)Dec 3, 2021Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Dec 3, 2021