Medical Device Manufacturer · TW , Taichung, R.O.C.

Well-Life Healthcare, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2002

Recent clearances: DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B, THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302), DIGI-PRO TENS, MODEL WL-2204 AND WL-2205

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Well-Life Healthcare, Inc. Neurology ✕

5 devices

1-5 of 5

Cleared May 27, 2004

LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND...

Neurology · 90d

Cleared Dec 19, 2003

T-TECH DIGITAL, MODEL WL-22XXA SERIES

Neurology · 8d

Cleared Mar 20, 2003

DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B

Neurology · 28d

Cleared Dec 30, 2002

THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403),...

Neurology · 361d

Cleared Apr 30, 2002

DIGI-PRO TENS MODEL WL-2203 AND WL-2205

Neurology · 90d