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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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156 records meeting your search criteria returned- Product Code: KWQ Product Problem: Device Slipped Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
GLOBUS MEDICAL, INC. RESONATE 05/07/2022
MEDOS INTERNATIONAL SàRL CH UNKNOWN SCREWS 04/06/2022
GLOBUS MEDICAL, INC. RESONATE 03/03/2022
GLOBUS MEDICAL, INC. RESONATE 02/08/2022
GLOBUS MEDICAL, INC. RESONATE 02/08/2022
GLOBUS MEDICAL, INC. RESONATE 01/05/2022
GLOBUS MEDICAL, INC. RESONATE EXTREME ANGLE ANTERIOR CERVICAL 11/22/2021
GLOBUS MEDICAL, INC. RESONATE 11/22/2021
GLOBUS MEDICAL, INC. RESONATE EXTREME ANGLE ANTERIOR CERVICAL 11/11/2021
GLOBUS MEDICAL, INC. RESONATE 09/22/2021
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