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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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418 records meeting your search criteria returned- Product Code: OIY Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ATTUNE PS FEM RT SZ 8 CEM 08/11/2021
DEPUY IRELAND - 9616671 ATTUNE PS FB INSRT SZ 8 18MM 08/11/2021
DEPUY IRELAND - 9616671 ATTUNE PS FB INSRT SZ 4 10MM 08/06/2021
DEPUY IRELAND - 9616671 ATTUNE PS FEM LT SZ 4 NAR CEM 08/06/2021
DEPUY IRELAND - 9616671 ATTUNE CR FEM RT SZ 6 CEM 08/06/2021
DEPUY IRELAND - 9616671 ATTUNE PS FB INSRT SZ 6 6MM 08/06/2021
DEPUY IRELAND - 9616671 ATTUNE MEDIAL ANAT PAT 38MM 08/06/2021
ZIMMER BIOMET, INC. VNGD CR LIP TIB BRG 16X71/75MM 08/05/2021
ZIMMER BIOMET, INC. BIOMET ILOK PRI TIB TRAY 71MM 08/05/2021
ZIMMER BIOMET, INC. BIOMET FINNED PRI STEM 40MM 08/05/2021
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