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

Manufacturer and User Facility Device Experience (MAUDE)
  • 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 
 4 
 5 
 6 
 7 
 8 
 9 
 > 
 
86 records meeting your search criteria returned- Product Code: HRS Product Problem: Failure to Osseointegrate Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
KARL LEIBINGER MEDIZINTECHNIK GMBH & CO. LEVEL ONE THORACIC 03/02/2018
KARL LEIBINGER MEDIZINTECHNIK GMBH & CO. LEVEL ONE THORACIC 02/15/2018
BIOMET TRAUMA PEG STANDARD 4.0X45.0MM 10/27/2016
BIOMET TRAUMA PEG STANDARD 4.0X55.0MM 10/27/2016
BIOMET TRAUMA PEG STANDARD 4.0X42.5MM 10/27/2016
BIOMET TRAUMA S3 SHOULDER PLATE 4 HOLE LEFT 10/27/2016
BIOMET TRAUMA PEG STANDARD 4.0X55.0MM 10/27/2016
BIOMET TRAUMA SCREW MULTIDIRECTION 3.8X32MM 10/27/2016
BIOMET TRAUMA SCREW MULTIDIRECTION 3.8X34MM 10/27/2016
BIOMET TRAUMA PEG STANDARD 4.0X35.0MM 10/27/2016
-
-