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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
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80 records meeting your search criteria returned- Product Code: MBI Product Problem: Unintended Movement Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
ARTHREX, INC. DOUBLE LOADED KNOTLESS FIBERTAK, KNEE 02/22/2024
ARTHREX, INC. IMPLANT SYSTEM, SUTURELOC 01/02/2024
ARTHREX, INC. SELF BUNCHING KL 1.8 FIBERTAK, HIP 12/14/2023
MEDOS INTERNATIONAL SàRL TRUESPAN 24 DEGREE PEEK 12/13/2023
ARTHREX, INC. KL 1.8 FIBERTAK, SHOULDER 12/08/2023
ARTHREX, INC. SP FBRTAK RC FBRTPE BLK/BLU & STTPE BLU 12/06/2023
MEDOS INTERNATIONAL SARL TRUESPAN 24 DEGREE PEEK 12/06/2023
MEDOS INTERNATIONAL SARL TRUESPAN 24 DEGREE PEEK 12/06/2023
MEDOS INTERNATIONAL SARL TRUESPAN 12 DEGREE PEEK 12/06/2023
MEDOS INTERNATIONAL SARL TRUESPAN 24 DEGREE PEEK 12/04/2023
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