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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.
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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US UNK - IMPLANT 02/27/2024
MEDOS INTERNATIONAL SàRL 5.5 HEALIX ADVANCE KNTLS BR 01/31/2024
DEPUY MITEK LLC US 5.5 HEALIX ADVANCE BR W/OC 01/31/2024
MEDOS INTERNATIONAL SàRL 4.5HLX ADV BR ANC-DYNA 3-SUT 12/19/2023
DEPUY MITEK LLC US UNK - IMPLANT 12/19/2023
DEPUY MITEK LLC US UNK - IMPLANT 12/19/2023
DEPUY MITEK LLC US UNK - IMPLANT 12/19/2023
DEPUY MITEK LLC US UNK - IMPLANT 12/19/2023
DEPUY MITEK LLC US 6.5 HEALIX ADVANCE KNTLS BR 12/13/2023
DEPUY MITEK LLC US UNK - IMPLANT 12/12/2023
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