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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
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7 records meeting your search criteria returned- Product Code: HNQ Patient Problem: Foreign Body In Patient Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 09/11/2019
CARL ZEISS MEDITEC CATARACT TECHNOLOGY, MILOOP LENS FRAGMENTATION DEVICE 05/17/2019
WECK / TELEFLEX MEDICAL INC. WECK OPHTHALMIC MUSCLE HOOK 05/17/2019
IANTECH, INC. MILOOP LENS FRAGMENTATION DEVICE 10/02/2018
IANTECH, INC. MILOOP LENS FRAGMENTATION DEVICE 09/13/2018
IANTECH, INC. MILOOP LENS FRAGMENTATION DEVICE 09/05/2018
KATENA PRODUCTS INC. ROSEN CHOPPER 09/14/2016
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