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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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62 records meeting your search criteria returned- Product Code: MAI Product Problem: Entrapment of Device Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US BIOKNOTLESS PLUS W/OC 02/07/2020
ARTHREX, INC. SUTURE ANCHOR, BIO- COMPOSITE PUSHLOCK 12/02/2019
DEPUY MITEK LLC US 5.5 HEALIX BR ANCHOR W/OCORD 11/20/2019
DEPUY MITEK LLC US LUPINE LOOP RAPIDE ANCHOR W/ORTHOCORD DS 06/28/2019
ARTHREX, INC. INTERNALBRACE LIGAMENT 05/13/2019
DEPUY MITEK LLC US OMNISPAN MENISCAL REPAIR 12DEG 05/09/2019
DEPUY MITEK LLC US MILAGRO INSCR SMALL SIZE 5X30 04/12/2019
DEPUY MITEK LLC US MILAGRO INSCR SMALL SIZE 5X30 04/12/2019
ARTHREX, INC. BIO-COMP INTERFSCRW W/DISP SHTH 02/19/2019
DEPUY MITEK LLC US GRYPHON P BR DSW PERMACORD 12/07/2018
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