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Well-Life Healthcare, Inc.

Last updated May 23, 2026

What Well-Life Healthcare, Inc. makes

Well-Life Healthcare, Inc. manufactures line-powered transcutaneous electrical nerve stimulation (TENS) systems for physical therapy, including digital and limited-function models. Examples include the DIGI-PRO TENS series (WL-2203B, WL-2204B, WL-2205B), THE IZZZY-TENS, THE SLIM-TENS, and THE MENS-TENS, as well as T-TECH DIGITAL units in the WL-22XXA series. These devices are designed for pain management and muscle stimulation.

The company’s TENS systems are classified as Class II devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. The portfolio is regulated in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
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Catalogue (44)

Device	Model / Reference	Registries	Class	Status
Well-Life	WL-2504	FDA UDI	Class II	Unknown
Well-Life	WL-2407	FDA UDI	Class II	Unknown
Well-Life	WL-2406	FDA UDI	Class II	Unknown
Well-Life	WL-2205	FDA UDI	Class II	Unknown
Well-Life	WL-2301	FDA UDI	Class II	Unknown
Well-Life	WL-2204	FDA UDI	Class II	Unknown
Well-Life	WL-2104	FDA UDI	Class II	Unknown
Well-Life	WR-2605	FDA UDI	Class II	Unknown
Well-Life	WL-2103	FDA UDI	Class II	Unknown
Well-Life	SP-5181	FDA UDI	Class II	Active
Well-Life	WL-2203	FDA UDI	Class II	Unknown
Well-Life	CM-5050	FDA UDI	Class II	Active
Well-Life	WL-2407Rx	FDA UDI	Class II	Unknown
Well-Life	WL-2102	FDA UDI	Class II	Unknown
Well-Life	WL-2405	FDA UDI	Class II	Unknown
Well-Life TENS/EMS/Heating Stimulator	K213091	FDA 510(k)	Class II	Active
Well-Life Otc Ems System	K102786	FDA 510(k)	Class II	Active
Otc Combo Tens/Ems System	K141299	FDA 510(k)	Class II	Active
Digi-Pro Tens/Wl-2203b, 2204b, 2204b-P1, 2204b-P2, 2205b	K030537	FDA 510(k)	Class II	Active
Otc Tens For Low Back Pain Relief, Model Wl-2405 And Wl-2406	K052785	FDA 510(k)	Class II	Active
Digi-Pro Tens Model Wl-2203 And Wl-2205	K021359	FDA 510(k)	Class II	Active
Well Life Self Adhesive Electrode / Models: Cm, Fa, Pu And Sp	K082065	FDA 510(k)	Class II	Active
Otc Patch	K133723	FDA 510(k)	Class II	Active
Otc Abdomen & Thigh System, Model: Wl-2410, Wl-2411 And Wl-2412	K072168	FDA 510(k)	Class II	Active
Mini Patch	K121353	FDA 510(k)	Class II	Active
Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe Electrode	K222528	FDA 510(k)	Class II	Active
Digi-Pro Tens, Model Wl-2204 And Wl-2205	K020314	FDA 510(k)	Class II	Active
OTC Combo TENS/EMS System	K172809	FDA 510(k)	Class II	Active
WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A	K161453	FDA 510(k)	Class II	Active
If True Sine Interferential Stimulator, Wl-2206d	K092763	FDA 510(k)	Class II	Active
If Series True Sine Interferential Stimulator, Model: Wl-2206b And Wl-2106e	K090023	FDA 510(k)	Class II	Active
Otc Tens For Low Back Pain Relief, Model Wl-2407	K063660	FDA 510(k)	Class II	Active
Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimulator; Well-Life Pain Relief Stimulator; Menstrual Plus Stimulator	K233054	FDA 510(k)	Class II	Active
Buttock Muscle Stimulator Model Wl-2413b; Buttock Muscle Stimulator Mode Wl-2413e	K123075	FDA 510(k)	Class II	Active
The Izzzy-Tens (wl-2401), The Slim-Tens (wl-2402), The Mens-Tens (wl2403), The Compact Tens (wl-2302)	K020020	FDA 510(k)	Class II	Active
WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A and WR-2605/2605A	K162663	FDA 510(k)	Class II	Active
Otc Tens For Arm And Leg Pain Relief, Model Wl-2407	K091757	FDA 510(k)	Class II	Active
Pro Tens, Model Wl-240 Rx	K080304	FDA 510(k)	Class II	Active
Limited Function Wl/Otc-Tens Device, Model Wl-2103a, Wl-2203a, Wl-2203b And Wl-2401	K040512	FDA 510(k)	Class II	Active
Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)	K220524	FDA 510(k)	Class II	Active
Well-Life Garment Electrodes (GM Series)	K200942	FDA 510(k)	Class II	Active
4 Channels Multiple Model Digital Electrical Stimulator, Model Nuvostim Iv, Wl-2504a	K100399	FDA 510(k)	Class II	Active
Well-Life Incontinence Stimulation System (WL-2405i(P))	K251760	FDA 510(k)	Class II	Active
T-Tech Digital, Model Wl-22xxa Series	K033857	FDA 510(k)	Class II	Active

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FDA Establishments (1)

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Well-Life Healthcare Limited Jhonghe Taipei · TW FEI 3006850006