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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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10 records meeting your search criteria returned- Product Code: KWD Patient Problem: Failure of Implant Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ARTHROSURFACE, INC. PROSTHESIS, TOE, HEMI-, PHALANGEAL 09/24/2020
WRIGHT MEDICAL TECHNOLOGY, INC. CARTIVA IMPLANT 08/02/2019
CARTIVA, INC. CARTIVA IMPLANTS 07/31/2019
CARTIVA, INC. CARTIVA IMPLANTS 07/31/2019
CARTIVA, INC. CARTIVA 07/08/2019
TRILLIANT SURGICAL 3S HEMI IMPLANT, MEDIUM, NON-STERILE 07/02/2019
WRIGHT MEDICAL TECHNOLOGY, INC. CARTIVA IMPLANT 06/25/2019
VILEX IN TENNESSEE, INC. VILEX IMPLANT 11/15/2017
ASCENSION ORTHOPEDICS MGT MOVEMENT PROX. PHAL. TOTAL SZ. 40 01/13/2016
VILEX, INC. VILEX CANNULATED MET HEAD IMPLANT 03/03/2015
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