Easymed Instruments Co., Ltd. FDA Approvals

0 new drug approvals and 2 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
Pelvic Floor Stimulator (Intrelief PFE)510(k)Nov 27, 2024Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Nov 27, 2024
Intrelief510(k)Dec 30, 2021Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Dec 30, 2021