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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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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 10/16/2023
DEPUY MITEK LLC US UNK - IMPLANT 10/13/2023
MEDOS INTERNATIONAL SARL 5.5 HEALIX ADVANCE KNTLS BR 10/13/2023
MEDOS INTERNATIONAL SARL 4.5HLX ADV BR ANC-DYNA 3-SUT 10/13/2023
MEDOS INTERNATIONAL SARL 4.75 HEALIX ADVANCE KNTLS BR 10/13/2023
DEPUY MITEK LLC US 5.5 HEALIX ADVANCE BR3SUT W/OC 10/04/2023
MEDOS INTERNATIONAL SàRL 6.5 HEALIX ADVANCE KNTLS BR 10/04/2023
MEDOS INTERNATIONAL SàRL HEALIX AV BR 5.5 TAPE WHT/BLUE 10/04/2023
MEDOS INTERNATIONAL SàRL 5.5MM HEALX ADV SP BIOC ANCHOR 10/04/2023
MEDOS INTERNATIONAL SàRL 5.5 HEALIXADV BR3SUTANC PCORD 10/04/2023
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