• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
163 records meeting your search criteria returned- Product Code: KRO Patient Problem: Joint Laxity Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER ORTHOPAEDICS-MAHWAH MRHK TIB INS 10MM XS/S S1/S2 05/17/2023
WALDEMAR LINK GMBH & CO. KG ENDO-MODEL SL KNEE PROTHESIS SYSTEM 05/09/2023
ONKOS SURGICAL ELEOS 05/01/2023
ONKOS SURGICAL ELEOS 05/01/2023
ONKOS SURGICAL ELEOS 05/01/2023
STANMORE IMPLANTS WORLDWIDE DISTAL FEMUR - AXLE 04/24/2023
DEPUY ORTHOPAEDICS INC US LPS UNIV TIB HIN INS XSM 16MM 04/11/2023
WALDEMAR LINK GMBH & CO. KG ENDO-MODEL SL NON-ROTATIONG HINGE KNEE P 03/23/2023
DEPUY ORTHOPAEDICS INC US LPS UNIV TIB HIN INS XSM 18MM 03/07/2023
MEDACTA INTERNATIONAL SA GMK-HINGE FIXED TIBIAL INSERT SIZE 4/17M 03/01/2023
-
-