• 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 
 > 
 
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
AESCULAP AG CASPAR RONGEURSTRSERR 2X12MM160MM 10/02/2019
AESCULAP AG LEMPERT BONE RONGEUR CVD 200MM 06/28/2019
AESCULAP AG CASPAR RONGEURUP-BITESERR 3MM160MM 06/11/2019
ZIMMER BIOMET SPINE INC. RONGEUR PITUITARY CER BLACK SERRATED 3MM 05/14/2019
ZIMMER BIOMET SPINE INC. KERRISON RONGEUR BLACK 5MM LATERAL 02/19/2019
INTEGRA YORK, PA INC. RONGEUR,UNKNOWN 02/08/2019
ZIMMER BIOMET SPINE INC. RONGEUR PITUITARY CER BLACK SERRATED 3MM 11/13/2018
ZIMMER BIOMET SPINE INC. PITUITARY RONGEUR BLACK 3MM LATERAL 10/03/2018
ZIMMER BIOMET SPINE INC. PITUITARY RONGEUR BLACK 3MM LATERAL 09/13/2018
ZIMMER BIOMET SPINE INC. PITUITARY RONGEUR BLACK 3MM LATERAL 09/12/2018
-
-