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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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11 records meeting your search criteria returned- Product Code: KNH Product Problem: Positioning Failure Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
OLYMPUS / GYRUS ACMI BAND FALOPE RING 04/25/2018
GYRUS ACMI, INC FBK DUAL INC. W/O TROCAR 8/PK 09/01/2017
COOPERSURGICAL, INC. FILSHIE 04/03/2017
OSTA FBK DUAL INC. W/TROCAR 8/PK 01/26/2017
OSTA FBK DUAL INC. W/TROCAR 8/PK 08/17/2016
BAYER HEALTHCARE LLC DEVICE, OCCLUSION, TUBAL 04/14/2016
BAYER HEALTHCARE LLC DEVICE, OCCLUSION, TUBAL, CONTRACEPTIVE 04/14/2016
BAYER HEALTHCARE LLC ESSURE 03/21/2016
BAYER HEALTHCARE LLC ESSURE 12/04/2014
BAYER HEALTHCARE LLC ESSURE 10/07/2014
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