Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
 1 
 2 
 3 
 > 
 
26 records meeting your search criteria returned- Product Code: JDR Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. TWINFIX TI 3.5 ULTRABRAID 11/15/2022
SMITH & NEPHEW, INC. TWINFIX TI 5.0 ULTRABRAID 07/07/2022
SMITH & NEPHEW, INC. TWINFIX TI 5.0 ULTRABRAID 06/22/2022
SMITH & NEPHEW, INC. OSTEORAPTOR 2.3 W. UB COBRAID BLUE 05/30/2022
SMITH & NEPHEW, INC. TWINFIX TI 5.0 ULTRABRAID 03/04/2022
SMITH & NEPHEW, INC. TWINFIX TI 2.8 ULTRABRAID 02/15/2022
SMITH & NEPHEW, INC. OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE 02/14/2022
SMITH & NEPHEW, INC. TWINFIX TI 5.0 ULTRABRAID 01/13/2022
SMITH & NEPHEW, INC. TWINFIX ULTRA PK 4.5MM W/2 UB -WHT &BL 12/24/2021
SMITH & NEPHEW, INC. TWINFIX TI 5.0 ULTRABRAID 11/30/2021
-
-