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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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10 records meeting your search criteria returned- Product Code: HWQ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. UNKNOWN ENDOBUTTON DEVICE 09/14/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - CONSTRUCTS: CSLP 07/12/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC 3.5MM CORTEX SCREW SELF-TAPPING 80MM 02/03/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC 3.5MM CORTEX SCREW SELF-TAPPING 80MM 02/03/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC 3.5MM CORTEX SCREW SELF-TAPPING 40MM 02/03/2021
SYNTHES GMBH 4.0MM TI CANCELLOUS BONE SCREW FULLY 12/03/2020
SYNTHES GMBH 4.0MM TI CANCELLOUS BONE SCREW FULLY 12/03/2020
STRYKER ENDOSCOPY-SAN JOSE SLINGSHOT 70 DEG UP 02/10/2020
STRYKER ENDOSCOPY-SAN JOSE NANOPASS REACH CRESCENT 12/09/2019
ARTHROCARE CORP. DISP FIRSTPASS STR PASSR SELF 02/08/2019
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