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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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218 records meeting your search criteria returned- Product Code: JDR Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
SYNTHES TRAUMA : CROSSROADS EXTREMITY SY DYNAFORCE IS A NITINOL SUPERELASTIC BONE 12/27/2022
SMITH & NEPHEW, INC. SPYROMITE 2.0 PK W/1 2-0 ULTRABRAID WH 12/26/2022
SMITH & NEPHEW, INC. MNITAC 2.0 TI W/NDL 22-0 ULTRABRAID 12/06/2022
SMITH & NEPHEW, INC. TWINFIX TI 3.5 ULTRABRAID 11/17/2022
SMITH & NEPHEW, INC. TWINFIX ULTRA HA 4.5 W/2 UB (WH & BLUE 11/16/2022
SMITH & NEPHEW, INC. UNKNOWN METAL SUTURE ANCHOR 11/04/2022
SMITH & NEPHEW, INC. UNKNOWN METAL SUTURE ANCHOR 11/04/2022
SMITH & NEPHEW, INC. UNKNOWN METAL SUTURE ANCHOR 11/03/2022
SMITH & NEPHEW, INC. UNKNOWN METAL SUTURE ANCHOR 11/03/2022
SMITH & NEPHEW, INC. UNKN METAL SUTURE ANCHOR 11/02/2022
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