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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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187 records meeting your search criteria returned- Product Code: DTB Product Problem: Use of Device Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
GREATBATCH MEDICAL MYOPORE 08/09/2023
ABBOTT MEDICAL TENDRIL DX 08/09/2023
CARDIAC PACEMAKERS, INC BIPOLAR ENDOCARDIAL LEAD 08/09/2023
BOSTON SCIENTIFIC CORPORATION FINELINE II STEROX LEADS 07/14/2023
BOSTON SCIENTIFIC CORPORATION FINELINE II EZ STEROX 06/21/2023
BOSTON SCIENTIFIC CORPORATION FINELINE II EZ STEROX 06/12/2023
MEDTRONIC SINGAPORE OPERATIONS CAPSUREFIX NOVUS LEAD MRI SURESCAN 03/23/2023
BOSTON SCIENTIFIC CORPORATION FINELINE II EZ STEROX 11/07/2022
BOSTON SCIENTIFIC CORPORATION FINELINE II EZ STEROX 10/03/2022
MPRI CAPSUREFIX NOVUS LEAD MRI SURESCAN 09/07/2022
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