• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 
 
89 records meeting your search criteria returned- Product Code: HTX Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIFE INSTRUMENT CORP. unknown brand name 12/02/2014
AESCULAP AG&CO KG KERRISON BLK COATED 130 UP 180X1MM THIN 11/21/2014
SYNTHES TUTTLINGEN DISC RONGEUR STRAIGHT/4MM WIDTH 09/26/2014
SYMMETRY SURGICAL RAPIDCLEAN CERAMIC COATED CONVERTIBLE KE 07/29/2014
SYMMETRY SURGICAL RAPIDCLEAN MICRO KERRISON RONGEUR 07/29/2014
V MUELLER NEURO/SPINE KERRISON RONJURE 07/17/2014
SYNTHES TUTTLINGEN DISC RONGEUR STRAIGHT WITHOUT DISC RONGE 07/14/2014
AESCULAP, INC. RONGEUR 05/28/2014
SYMMETRY SURGICAL INC SSI MICRO KERRISON RONGEUR 01/07/2014
-
-