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
 

 
 
8 records meeting your search criteria returned- Product Code: JDR Product Problem: Unintended Movement Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PARAGON28, INC JAWS NITINOL STAPLE SYSTEM 01/24/2024
PARAGON28, INC JAWS NITINOL STAPLE SYSTEM 01/24/2024
DEPUY MITEK LLC US MINI QA+ #2/O OCORD V-5 01/26/2022
CROSSROADS EXTREMITY SYSTEMS DYNAFORCE MPJ SYSTEM 08/12/2019
SMITH & NEPHEW, INC. MNITAC,2.0 TI W/NDL,2#2-0 ULTRABRAID 06/17/2019
WRIGHTS LANE SYNTHES USA PRODUCTS LLC SPEED COMPRESSION IMPLANT KIT 09X07X07MM 10/10/2018
WRIGHTS LANE : SYNTHES USA PRODUCTS LLC STAPLE, FIXATION, BONE 12/14/2017
BIOMET ORTHOPEDICS MAXFIRE MARXMEN CURVED 11/19/2014
-
-