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

Well-Life Healthcare, Inc. has 6 FDA 510(k) cleared medical devices. Based in Taichung, R.O.C., TW.

Historical record: 6 cleared submissions from 2002 to 2004. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Well-Life Healthcare, Inc. Filter by specialty or product code using the sidebar.

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

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