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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
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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80 records meeting your search criteria returned- Product Code: MAI Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US GRYPHON P BR DS ANCHOR W/OC 02/14/2024
DEPUY MITEK LLC US OMNISPAN MENISCAL REPAIR 12DEG 02/09/2024
DEPUY MITEK LLC US 4.5 HEALIX ADVANCE BR W/OCORD 02/01/2024
DEPUY MITEK LLC US GRYPHON P BR ANCHOR W/OC 01/25/2024
DEPUY MITEK LLC US 4.5 HEALIX BR ANCHOR W/OCORD 01/17/2024
DEPUY MITEK LLC US LUPINELOOPPLUS ANCHOR W/OC DS 11/30/2023
DEPUY MITEK LLC US LUPINE BR DS W/ORTHCRD 10/19/2023
DEPUY MITEK LLC US GRYPHON P BR DS ANCHOR W/OC 10/18/2023
DEPUY MITEK LLC US GRYPHON P BR DS ANCHOR W/OC 10/18/2023
DEPUY MITEK LLC US LUPINELOOPPLUS ANCHOR W/OC DS 09/12/2023
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