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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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441 records meeting your search criteria returned- Product Code: NIO Product Problem: Difficult to Remove Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR OMNILINK ELITE PERIPHERAL STENT SYSTEM 03/17/2022
ABBOTT VASCULAR OMNILINK ELITE PERIPHERAL STENT SYSTEM 03/14/2022
ABBOTT VASCULAR OMNILINK ELITE PERIPHERAL STENT SYSTEM 03/08/2022
CORDIS CORPORATION SMART CONTROL, ILIAC 8X100 01/24/2022
CORDIS CORPORATION SMART CONTROL, ILIAC 8X40 01/16/2022
BOSTON SCIENTIFIC CORPORATION EXPRESS LD ILIAC / BILIARY 01/07/2022
ATRIUM MEDICAL CORPORATION ADVANTA V12 COVERED STENT 01/06/2022
ATRIUM MEDICAL CORPORATION ADVANTA V12 COVERED STENT 12/29/2021
ATRIUM MEDICAL CORPORATION ADVANTA V12 COVERED STENT 12/28/2021
ABBOTT VASCULAR OMNILINK ELITE PERIPHERAL STENT SYSTEM 11/10/2021
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