• 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 
 > 
 
61 records meeting your search criteria returned- Product Code: OJH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER KNEE CREATIONS, INC. KNEE CREATIONS SUBCHONDROPLASTY KNEE KIT 12/29/2020
ZIMMER KNEE CREATIONS, INC. CPLT F&A KIT 3CC 15G END 10/14/2020
ZIMMER KNEE CREATIONS, INC. KNEE CREATIONS SUBCHONDROPLASTY FOOT & A 09/22/2020
ZIMMER KNEE CREATIONS, INC. SUBCHONDROPLASTY ACCUFILL KNEE KIT 5CC 1 09/09/2020
ZIMMER KNEE CREATIONS, INC. SUBCHONDROPLASTY 04/28/2020
ZIMMER KNEE CREATIONS, INC. SUBCHONDROPLASTY 03/26/2020
ZIMMER KNEE CREATIONS, INC. CPLT F&A KIT 3CC 11G END 03/26/2020
ZIMMER KNEE CREATIONS, INC. CPLT F&A KIT 3CC 11G END 02/19/2020
ZIMMER KNEE CREATIONS, INC. SUBCHONDROPLASTY 01/14/2020
ZIMMER KNEE CREATIONS, INC. SUBCHONDROPLASTY 01/10/2020
-
-