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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
EXACTECH, INC. GLENOSPHERE, 36MM 11/07/2023
EXACTECH, INC. SPECIFIC DEVICE NOT REPORTED 11/07/2023
EXACTECH, INC. EQUINOXE REVERSE 38MM HUMERAL LINER +2.5 11/03/2023
EXACTECH, INC. SPECIFIC DEVICE NOT REPORTED 11/03/2023
DEPUY ORTHOPAEDICS INC US UNK SHOULDER GLENOID GLOBAL APG+ 11/01/2023
EXACTECH, INC. EQUINOXE REVERSE 42MM GLENOSPHERE 10/27/2023
ZIMMER BIOMET, INC. UNK HEAD 10/25/2023
EXACTECH, INC. SPECIFIC DEVICE NOT REPORTED 10/23/2023
ZIMMER BIOMET, INC. ZIMMER TRABECULAR METAL REVERSE SHOULDER 10/23/2023
EXACTECH, INC. EQUINOXE REVERSE 42MM HUMERAL LINER +2.5 10/23/2023
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