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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 ORTHOPAEDICS INC US ENDURON NEUT 48OD X 28ID 02/29/2024
DEPUY ORTHOPAEDICS INC US ENDURON 10D 56 OR 68ODX28ID 01/02/2024
DEPUY ORTHOPAEDICS INC US ENDURON 10D 56 OR 68ODX28ID 12/07/2023
DEPUY ORTHOPAEDICS INC US ENDURON 10D 54OD X 28ID 12/07/2023
DEPUY ORTHOPAEDICS INC US ENDURON 10D 60 OR 72ODX28ID 12/01/2023
DEPUY ORTHOPAEDICS INC US ENDURON NEUT 50OD X 28ID 10/18/2023
DEPUY ORTHOPAEDICS INC US ENDURON NEUT 52OD X 28ID 09/13/2023
SMITH AND NEPHEW RICHARDS REFLECTION 08/12/2023
SMITH & NEPHEW ORTHOPAEDICS AG POLARCUP PE INSERT 51/28 NON-CEM 07/22/2022
SMITH & NEPHEW ORTHOPAEDICS AG POLARCUP PE INSERT 49/28 NON-CEM 07/21/2022
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