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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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111 records meeting your search criteria returned- Product Code: HWT Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN RECAP CUP 03/09/2023
DEPUY ORTHOPAEDICS INC US UNKNOWN SHOULDER HUMERAL HEADS 02/14/2023
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE TIBIAL INSERT 02/13/2023
DEPUY IRELAND - 9616671 UNK KNEE TIBIAL INSERT ATTUNE REVISION 11/07/2022
DEPUY IRELAND - 9616671 ATTUNE MES SIZING/ROT GDE 09/19/2022
DEPUY IRELAND - 9616671 ATTUNE FEM NAR POR PS RT SZ 6 08/17/2022
DEPUY IRELAND - 9616671 ATTUNE RP PS ARTIC SURF SZ4 08/11/2022
DEPUY IRELAND - 9616671 ATTUNE DIST FEM AUG SZ 6 4MM 08/10/2022
DEPUY ORTHOPAEDICS INC US UNK ALIGNMENT DEVICE 08/05/2022
DEPUY IRELAND - 9616671 UNK SHOULDER HUMERAL EPIPHYSIS DELTA XTE 08/05/2022
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