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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
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84 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
MEDOS INTERNATIONAL SARL 6.5 HEALIX ADV SP PEEK CE 07/01/2021
DEPUY MITEK LLC US LUPINE BR W/ORTHCRD 06/25/2021
DEPUY MITEK LLC US LUPINE BR DS W/ORTHCRD 06/21/2021
MEDOS INTERNATIONAL SARL 5.5MM HEALX ADV SP BIOC ANCHOR 06/21/2021
DEPUY MITEK LLC US LUPINE BR DS W/ORTHCRD 06/21/2021
DEPUY MITEK LLC US 4.5 HEALIX PEEK ANCH.W/OCORD 05/06/2021
DEPUY MITEK LLC US LUPINE BR W/ORTHCRD 04/12/2021
DEPUY MITEK LLC US OMNISPAN MENISCAL REPAIR 27DEG 03/09/2021
DEPUY MITEK LLC US LUPINE LOOP PLUS ANCHOR W/OC 01/14/2021
DEPUY MITEK LLC US LUPINE BR DS W/ORTHCRD 12/28/2020
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