• 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 
 4 
 > 
 
38 records meeting your search criteria returned- Product Code: KKY Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MATRIX SURGICAL USA OMNIPORE SURGICAL IMPLANT - TWO-PIECE CH 02/07/2019
BIOMET MICROFIXATION HTR * PMI GOBIEN LEFT FRONTAL SPHENOID P 09/06/2018
BIOMET MICROFIXATION HTR * PMI GOBIEN RIGHT FRONTAL SPHENOID 09/06/2018
BIOMET MICROFIXATION HTR * PMI HARSCH LEFT FRONTAL SPHENOID P 09/06/2018
OXFORD PERFORMANCE MATERIALS HTR-PEKK 07/19/2018
OXFORD PERFORMANCE MATERIALS HTR-PEKK 07/19/2018
BIOMET MICROFIXATION HTR * PMI ACEBO SAENZ BI-FRONTAL PARIETA 01/03/2018
BIOMET MICROFIXATION HTR-PMI KOVALIOVAS LEFT FRONTAL SPHENOID 12/12/2017
BIOMET MICROFIXATION HTR-PMI KOVALIOVAS RIGHT FRONTAL SPHENOI 12/12/2017
BIOMET MICROFIXATION HARD TISSUE REPLACEMENT-PATIENT MATCHED 05/25/2017
-
-