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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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87 records meeting your search criteria returned- Product Code: GZJ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. TENS 7000 DIGITAL 07/06/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. LG 06/30/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. INTENSITY 10 DIGITAL TENS 06/09/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. INTENSITY 10 DIGITAL TENS 06/09/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. INTENSITY 10 DIGITAL TENS 05/26/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. INTENSITY 10 DIGITAL TENS 05/18/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. INTENSITY 10 DIGITAL TENS 05/12/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. QUATTRO 2.5 05/12/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. QUATTRO 2.5 05/12/2017
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. QUATTRO 2.5 05/11/2017
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