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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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99 records meeting your search criteria returned- Product Code: MDM Product Problem: Difficult to Remove Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. ARTHREX SCORPION-MULTIFIRE NEEDLE 07/11/2023
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 03/02/2023
BIOMET ORTHOPEDICS, LLC 3.5 MM SWIVEL HEX RATCHET SHAFT 01/30/2023
ARTHREX, INC. DISP INSTRS KIT FOR MINI S-TAK 01/03/2023
ARTHREX, INC. DRIVER, T10 HEXALOBE 11/07/2022
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 10/24/2022
ARTHREX, INC. SUREFIRE SCORPION NEEDLE 08/08/2022
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 07/18/2022
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 07/18/2022
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 07/11/2022
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