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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. BONE SCR 6.5X30 SELF-TAP 04/18/2022
ZIMMER BIOMET, INC. SHELL POROUS WITH CLUSTER HOLES 56 MM O. 04/18/2022
ZIMMER BIOMET, INC. SHELL POROUS WITH CLUSTER HOLES 56 MM O. 04/18/2022
ZIMMER BIOMET, INC. BONE SCR 6.5X30 SELF-TAP 04/18/2022
ZIMMER BIOMET, INC. NTINUUM TM SHELL CLUST 56 KK 04/18/2022
SMITH & NEPHEW ORTHOPAEDICS AG BICON-PLUS TITANIUM SHELL 4-52 NON-CEM 04/18/2022
SMITH & NEPHEW ORTHOPAEDICS AG BICON-PLUS TITANIUM SHELL 3-49 NON-CEM 04/15/2022
STRYKER ORTHOPAEDICS-MAHWAH TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL 04/11/2022
STRYKER ORTHOPAEDICS-MAHWAH TRIDENTII TRITANIUM CLUSTER54E 03/04/2022
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_TRITANIUM CUP 03/03/2022
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