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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
ARTHREX, INC. 24MM BASEPLATE, MODULAR 04/09/2024
ZIMMER BIOMET, INC. UNK 36 GLENOSHERE 04/09/2024
ZIMMER BIOMET, INC. UNK 36 BEARING 04/09/2024
ARTHREX, INC. 36 +4 LAT/24 GLENOSPHERE 04/08/2024
ARTHREX, INC. 24MM BASEPLATE, MODULAR 04/08/2024
ARTHREX, INC. UNIVERS REVERS SPACER 36+6MM 04/08/2024
ARTHREX, INC. HUMERAL INSERT S/36 +3 TO FIT IN 36 CUP 04/08/2024
MEDACTA INTERNATIONAL SA REVERSE SHOULDER SYSTEM HUMERAL REVERSE 04/08/2024
TORNIER INC PERFORM REV INSERT SZ 1/2 39MM DIA +6 04/08/2024
DEPUY ORTHOPAEDICS INC US UNKNOWN SHOULDER HUMERAL CUP 04/04/2024
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