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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
ZIMMER BIOMET, INC. UNKNOWN SCREW 04/01/2024
ZIMMER BIOMET, INC. UNKNOWN SCREW 04/01/2024
ARTHREX, INC. 30MM CENTRAL SCREW, MODULAR 03/29/2024
ARTHREX, INC. 25MM CENTRAL SCREW, MODULAR 03/29/2024
ZIMMER BIOMET, INC. UNKNOWN GLENOID 03/27/2024
ZIMMER BIOMET, INC. UNKNOWN HUMERAL HEAD 03/27/2024
MEDACTA INTERNATIONAL SA REVERSE SHOULDER SYSTEM HUMERAL REVERSE 03/26/2024
ASCENSION ORTHOPEDICS, INC. 38MM REVERSE LINER +0 S 03/26/2024
TORNIER INC UNKNOWN PERFORM HUMERAL POLY 03/22/2024
DEPUY IRELAND - 3015516266 REVERSE HUMERAL SHELL L 40+0 03/21/2024
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