Well-Life Healthcare Limited
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 22
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K233054 | Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimula | October 18, 2024 |
| K222528 | Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/ | December 29, 2022 |
| K220524 | Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series) | August 4, 2022 |
| K213091 | Well-Life TENS/EMS/Heating Stimulator | February 19, 2022 |
| K200942 | Well-Life Garment Electrodes (GM Series) | June 1, 2021 |
| K172809 | OTC Combo TENS/EMS System | October 18, 2017 |
| K162663 | WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A and WR-2605/2605A | January 17, 2017 |
| K161453 | WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A | December 5, 2016 |
| K141299 | OTC COMBO TENS/EMS SYSTEM | November 14, 2014 |
| K133723 | OTC PATCH | January 28, 2014 |
| K123075 | BUTTOCK MUSCLE STIMULATOR MODEL WL-2413B; BUTTOCK MUSCLE STIMULATOR MODE WL-2413E | July 11, 2013 |
| K121353 | MINI PATCH | September 7, 2012 |
| K102786 | WELL-LIFE OTC EMS SYSTEM | July 1, 2011 |
| K100399 | 4 CHANNELS MULTIPLE MODEL DIGITAL ELECTRICAL STIMULATOR, MODEL NUVOSTIM IV, WL-2504A | June 25, 2010 |
| K091757 | OTC TENS FOR ARM AND LEG PAIN RELIEF, MODEL WL-2407 | February 5, 2010 |
| K092763 | IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D | October 8, 2009 |
| K082065 | WELL LIFE SELF ADHESIVE ELECTRODE / MODELS: CM, FA, PU AND SP | April 10, 2009 |
| K090023 | IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR, MODEL: WL-2206B AND WL-2106E | January 30, 2009 |
| K080304 | PRO TENS, MODEL WL-240 RX | June 20, 2008 |
| K072168 | OTC ABDOMEN & THIGH SYSTEM, MODEL: WL-2410, WL-2411 AND WL-2412 | December 19, 2007 |