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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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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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11 records meeting your search criteria returned- Product Code: NIQ Product Problem: Failure to Fold Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 06/29/2022
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 03/24/2022
ABBOTT VASCULAR XIENCE PROA EVEROLIMUS ELUTING CORONARY 08/19/2021
ABBOTT VASCULAR XIENCE PROA EVEROLIMUS ELUTING CORONARY 08/19/2021
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 08/21/2020
ABBOTT VASCULAR XIENCE PRIME 03/25/2020
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 08/01/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 08/01/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 07/30/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 07/30/2018
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