• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
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
WALDEMAR LINK GMBH & CO. KG ENDO-MODEL SL KNEE PROSTHESIS SYSTEM 07/25/2023
STRYKER ORTHOPAEDICS-MAHWAH GMRS DIST FEM COMP STD R 65MM 07/20/2023
ZIMMER BIOMET, INC. 12MM HEIGHT SIZE D ARTICULAR SURFACE WIT 07/19/2023
ONKOS SURGICAL INC. ELEOS LIMB SALVAGE SYSTEM 07/12/2023
WALDEMAR LINK GMBH & CO. KG ENDO-MODEL MODULAR KNEE PROSTHESIS SYSTE 06/27/2023
AESCULAP AG ENDURO MENISCAL COMPONENT F3 10MM 06/13/2023
WALDEMAR LINK GMBH & CO. KG ROTATIONAL KNEE PROSTHESIS ENDO-MODEL-M 06/06/2023
STANMORE IMPLANTS WORLDWIDE DISTAL FEMUR JTS 06/02/2023
DEPUY ORTHOPAEDICS INC US LPS UNIV TIB HIN INS XXSM 12MM 06/01/2023
DEPUY ORTHOPAEDICS INC US ATTUNE REV LPS INSRT XXSM 12MM 05/31/2023
-
-