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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
DT MEDTECH, A VILEX COMPANY HINTERMANN SERIES H3 TOTAL ANKLE REPLACE 06/26/2023
DT MEDTECH, A VILEX COMPANY HINTERMANN SERIES H3 TOTAL ANKLE REPLACE 06/26/2023
DT MEDTECH, A VILEX COMPANY HINTERMANN SERIES H3 TOTAL ANKLE REPLACE 06/26/2023
TRILLIANT SURGICAL, LLC D/B/A DJO FOOT A REVISION SLIDING CORE STAR ANKLE 11MM 03/16/2023
ENCORE MEDICAL, L.P. UNKNOWN STAR POLY 01/18/2023
ENCORE MEDICAL, L.P. SLIDING CORE, UHMPWE,9MM 12/27/2022
ENCORE MEDICAL, L.P. UNKNOWN STAR POLY 12/26/2022
ENCORE MEDICAL, L.P. UNKNOWN STAR POLY 12/20/2022
ENCORE MEDICAL, L.P. UNKNOWN STAR IMPLANT 12/13/2022
ENCORE MEDICAL, L.P. UNKNOWN STAR POLY 12/05/2022
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