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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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126 records meeting your search criteria returned- Product Code: KNH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
FEMCARE LTD. FILSHIE CLIPS 11/22/2022
HOLOGIC, INC. ADIANA PERMANENT CONTRACEPTION SYSTEM 02/17/2022
FEMCARE LTD. FILSHIE CLIP 12/16/2021
FEMCARE LTD. FILSHIE CLIPS 12/15/2021
Unknown Manufacturer TUBAL LIGATION 06/11/2021
COOPERSURGICAL, INC. FILSHIE CLIPS 05/10/2021
Unknown Manufacturer TUBAL LIGATION 03/16/2021
FEMCARE-NIKOMED LTD. FILSHIE CLIPS 02/17/2021
FEMCARE-NIKOMED LTD FILSHIE CLIPS 09/15/2020
FEMCARE LTD. FILSHIE CLIPS 09/09/2020
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