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Data / Medical devices / Taiwan / Well-Life Healthcare Limited

Well-Life Healthcare Limited: FDA-registered device maker in Jhonghe Taipei, Taiwan, 20 510(k) clearances

Well-Life Healthcare Limited is registered with the FDA (registration 3006850006) in Jhonghe Taipei, Taiwan. It lists 12 device types. The FDA files 20 510(k) clearances under its listings, the newest dated February 12, 2026. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this oneWatch Well-Life Healthcare Limited
FDA registration number
3006850006
Address
6F., No.168, Lide St., Jhonghe Taipei, Taiwan, 235
Owner or operator
Well-Life Healthcare Limited (10023740)
Roles
Contract manufacturer, Manufacturer, Specification developer
First device listed
December 12, 2007
Registered through
2026
Brand names listed
2103(Re)/4460.S, 4 Channels Multiple Modes Digital Electrical Stimulator /WL-2504A, Alimed, RM8216, Aurawave Mini, BeautyKo, Model BK#0078 X-Trim, Beurer, EM39, Bilt-Rite Orthopedics (Part# 10-65001), Bilt-Rite Part#10-65005 and more

Devices it lists

DeviceProduct codeClassRoleSource
Cable, ElectrodeIKD2Manufactureraccessdata.fda.gov
Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep HeatILX2Contract manufactureraccessdata.fda.gov
Electrode, CutaneousGXY2Manufacturer, Specification developeraccessdata.fda.gov
Interferential Current TherapyLIH2Manufactureraccessdata.fda.gov
Pad, Heating, PoweredIRT2Contract manufacturer, Manufactureraccessdata.fda.gov
PerineometerHIR2Manufactureraccessdata.fda.gov
Stimulator, Electrical, Non-Implantable, For IncontinenceKPI2Manufactureraccessdata.fda.gov
Stimulator, Electrical, Transcutaneous, For ArthritisNYN2Contract manufacturer, Manufactureraccessdata.fda.gov
Stimulator, Muscle, PoweredIPF2Manufactureraccessdata.fda.gov
Stimulator, Muscle, Powered, For Muscle ConditioningNGX2Contract manufacturer, Manufactureraccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain ReliefGZJ2Manufactureraccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-CounterNUH2Contract manufacturer, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
February 12, 2026K251760Well-Life Incontinence Stimulation System (WL-2405i(P))KPISubstantially EquivalentWell-Life Healthcare , Ltd.accessdata.fda.gov
October 18, 2024K233054Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimulator; Well-Life Pain Relief Stimulator; Menstrual Plus StimulatorNUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
December 29, 2022K222528Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe ElectrodeKPISubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
August 4, 2022K220524Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)NUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
February 19, 2022K213091Well-Life TENS/EMS/Heating StimulatorNUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
June 1, 2021K200942Well-Life Garment Electrodes (GM Series)GXYSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
January 17, 2017K162663WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A and WR-2605/2605AGZJSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
December 5, 2016K161453WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605ANUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
November 14, 2014K141299OTC COMBO TENS/EMS SYSTEMNUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
January 28, 2014K133723OTC PATCHNUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
September 7, 2012K121353MINI PATCHNUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
June 25, 2010K1003994 CHANNELS MULTIPLE MODEL DIGITAL ELECTRICAL STIMULATOR, MODEL NUVOSTIM IV, WL-2504AGZJSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
February 5, 2010K091757OTC TENS FOR ARM AND LEG PAIN RELIEF, MODEL WL-2407NUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
April 10, 2009K082065WELL LIFE SELF ADHESIVE ELECTRODE / MODELS: CM, FA, PU AND SPGXYSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
June 20, 2008K080304PRO TENS, MODEL WL-240 RXGZJSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
February 7, 2007K063660OTC TENS FOR LOW BACK PAIN RELIEF, MODEL WL-2407NUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
March 17, 2006K052785OTC TENS FOR LOW BACK PAIN RELIEF, MODEL WL-2405 AND WL-2406NUHSubstantially EquivalentWell-Life Healthcare Limitedaccessdata.fda.gov
May 27, 2004K040512LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401GZJSubstantially EquivalentWell-Life Healthcare, Inc.accessdata.fda.gov
December 19, 2003K033857T-TECH DIGITAL, MODEL WL-22XXA SERIESGZJSubstantially EquivalentWell-Life Healthcare, Inc.accessdata.fda.gov
July 27, 2001K002874WELL-TENSGZJSubstantially EquivalentWell-Life Consultantaccessdata.fda.gov

Compare with other makers

Updated February 12, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.