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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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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. 36 +6 / 33 COMBO HUMERAL INSERT 10/31/2023
ARTHREX, INC. 24MM +2 LAT BASEPLATE, MODULAR 10/30/2023
ARTHREX, INC. 35MM CENTRAL SCREW, MODULAR 10/30/2023
ZIMMER BIOMET, INC. COMP RVRS 25MM BSPLT HA+ADPTR 10/30/2023
ZIMMER BIOMET, INC. UNK GLENOID 10/26/2023
ZIMMER BIOMET, INC. UNK HUMERAL HEAD 10/26/2023
ZIMMER BIOMET, INC. UNK HUMERAL STEM 10/26/2023
ENCORE MEDICAL L.P. GLENOID, HEAD W/RETAINING SCREW, RSP, 36 10/23/2023
ENCORE MEDICAL L.P SCREW, RETAINING GLENOID HEAD RSP 10/20/2023
ZIMMER BIOMET, INC. COMP AUG MINI BSPLT W TPR MD 10/20/2023
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