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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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80 records meeting your search criteria returned- Product Code: MDM Product Problem: Entrapment of Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. RING CURRETTE,ANKLE ARTHRSCPY,REVSE ANGL 02/20/2023
BIOMET ORTHOPEDICS, LLC 3.5 MM SWIVEL HEX RATCHET SHAFT 01/30/2023
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 01/03/2023
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 01/03/2023
ARTHREX, INC. SCORPION MULTIFIRE NEEDLE 12/05/2022
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 12/02/2022
ARTHREX, INC. SCORPION NEEDLE, KNEE 11/28/2022
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 11/07/2022
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 11/07/2022
ARTHREX, INC. SCORPION-MULTIFIRE NEEDLE 09/12/2022
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