Well-Life Healthcare Limited FDA Approvals

0 new drug approvals and 5 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
Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimulator; Well-Life Pain Relief Stimulator; Menstrual Plus Stimulator510(k)Oct 18, 2024Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Oct 18, 2024
Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe Electrode510(k)Dec 29, 2022Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Dec 29, 2022
Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)510(k)Aug 4, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Aug 4, 2022
Well-Life TENS/EMS/Heating Stimulator510(k)Feb 19, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Feb 19, 2022
Well-Life Garment Electrodes (GM Series)510(k)Jun 1, 2021Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Jun 1, 2021