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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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120 records meeting your search criteria returned- Product Code: KWL Product Problem: Break Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ZIMMER SWITZERLAND MANUFACTURING GMBH CLS SPOTORNO, EXPANSION SHELL, UNCEMENTE 10/17/2022
OSTEOREMEDIES, LLC REMEDY SPECTRUM GV HIP SPACER 06/21/2022
OSTEOREMEDIES, LLC REMEDY SPECTRUM GV HIP SPACER 09/10/2021
OSTEOREMEDIES, LLC REMEDY SPECTRUM GV HIP SPACER 07/29/2021
OSTEOREMEDIES, LLC REMEDY HIP 05/10/2021
OSTEOREMEDIES, LLC REMEDY SPECTRUM GV HIP 12/30/2020
DEPUY INTERNATIONAL LTD - 8010379 ACTIS STD NK SZ4/5 10/19/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 4 10/18/2020
DEPUY IRELAND - 9616671 ACTIS RETAINING STEM INSERTER 10/15/2020
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 3 10/15/2020
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