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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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6 records meeting your search criteria returned- Product Code: MEH Patient Problem: Toxicity Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
DEPUY (IRELAND) ACTIS DUOFIX 06/16/2020
STRYKER CORP. REJUVENATE SPT MODULAR STEM 02/26/2020
STRYKER IRELAND OSTEONICS ACCOLADE TMZF PLUS HIPSTEM 11/27/2019
STRYKER ORTHOPAEDICS / HOWMEDICA OSTEONI ACCOLADE TMZF PLUS HIP STEM #3 10/01/2019
HOWMEDICA OSTEONICS CORP. AKA STRYKER OR STRYKER IMP HEAD V40 COCR 32MM + 4 LFIT 10/01/2019
HOWMEDICA OSTEONICS CORP AKA STRYKER ORT STRYKER ACCOLADE HIP STEM TMZF 04/08/2019
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