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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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120 records meeting your search criteria returned- Product Code: LRN Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
SYNTHES GMBH K-WIRE Ø1 W/DOUB TIP L150 SST 04/12/2022
SYNTHES GMBH UNK - CABLE/WIRE: CERCLAGE CABLE 03/15/2022
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - CABLE/WIRE 02/21/2022
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - CABLE/WIRE 01/25/2022
SYNTHES GMBH UNKNOWN - PINS/WIRES 10/25/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - CABLE/WIRE 10/12/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNK - CABLE/WIRE 10/01/2021
SYNTHES GMBH UNK - CABLE/WIRE 08/20/2021
WRIGHTS LANE SYNTHES USA PRODUCTS LLC UNKNOWN - PINS/WIRES 07/05/2021
SYNTHES GMBH UNKNOWN - PINS/WIRES 06/18/2021
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