Well-Life Healthcare, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251760 | Well-Life Incontinence Stimulation System (WL-2405i(P)) | February 12, 2026 |
| K040512 | LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401 | May 27, 2004 |
| K033857 | T-TECH DIGITAL, MODEL WL-22XXA SERIES | December 19, 2003 |
| K030537 | DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B | March 20, 2003 |
| K020020 | THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302 | December 30, 2002 |
| K020314 | DIGI-PRO TENS, MODEL WL-2204 AND WL-2205 | April 30, 2002 |
| K021359 | DIGI-PRO TENS MODEL WL-2203 AND WL-2205 | April 30, 2002 |