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 
 10 
 > 
 
312 records meeting your search criteria returned- Product Code: JWH Product Problem: Device Appears to Trigger Rejection Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDACTA INTERNATIONAL SA GMK-PRIMARY TIBIAL INSERT UC FIXED SIZE 04/30/2024
MEDACTA INTERNATIONAL SA GMK-SPHERIKA TIBIAL TRAY FIXED CEMENTED 04/25/2024
MEDACTA INTERNATIONAL SA GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SI 04/25/2024
MEDACTA INTERNATIONAL SA GMK-SPHERE 02.12.E0410FR TIBIAL INSERT F 04/12/2024
MEDACTA INTERNATIONAL SA GMK-SPHERE TIBIAL INSERT FIXED SPHERE FL 04/12/2024
MEDACTA INTERNATIONAL SA GMK-REVISION FIXED TIBIAL INSERT SC SIZE 04/11/2024
MEDACTA INTERNATIONAL SA GMK-REVISION 02.07.0310SCF FIXED TIBIAL 04/10/2024
MEDACTA INTERNATIONAL SA GMK-SPHERIKA TIBIAL INSERT FIXED SPHERE 04/09/2024
MEDACTA INTERNATIONAL SA GMK-SPHERE TIBIAL INSERT FIXED SPHERE FL 04/08/2024
MEDACTA INTERNATIONAL SA GMK-SPHERE TIBIAL INSERT FIXED SPHERE FL 04/05/2024
-
-