• 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 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
126 records meeting your search criteria returned- Product Code: KRO Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG AS ENDURO FEMORAL COMPONENT CEMENTED F1L 04/08/2020
ONKOS SURGICAL ELEOS SEGMENTAL STEM 04/02/2020
ONKOS SURGICAL ELEOS MALE-FEMALE MIDSECTION 04/01/2020
MEDACTA INTERNATIONAL SA GMK-HINGE FIXED TIBIAL INSERT SIZE 4/26M 02/04/2020
MEDACTA INTERNATIONAL SA GMK-HINGE FIXED TIBIAL INSERT SIZE 2/14M 01/08/2020
STANMORE IMPLANTS WORLDWIDE TROCHANTER PLATE SCREW. 29 MM 01/07/2020
MEDACTA INTERNATIONAL SA GMK-HINGE FIXED TIBIAL INSERT SIZE 4/12M 12/04/2019
STANMORE IMPLANTS WORLDWIDE DISTAL FEMUR JTS 11/28/2019
STANMORE IMPLANTS WORLDWIDE JTS DRIVE UNIT 11/21/2019
STANMORE IMPLANTS WORLDWIDE DISTAL FEMUR JTS 11/05/2019
-
-