• 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 
 > 
 
20 records meeting your search criteria returned- Product Code: KRO Patient Problem: Unspecified Tissue Injury Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US ATTUNE REV LPS INSRT XXSM 20MM 10/10/2023
DEPUY ORTHOPAEDICS INC US ATTUNE REV LPS INSRT XXSM 18MM 09/26/2023
DEPUY IRELAND - 9616671 ATTUNE REV LPS INSRT XSM 18MM 09/13/2023
DEPUY ORTHOPAEDICS INC US ATTUNE REV LPS INSRT XXSM 18MM 09/01/2023
DEPUY IRELAND - 9616671 ATTUNE REV LPS INSRT XXSM 14MM 07/26/2023
DEPUY ORTHOPAEDICS INC US ATTUNE REV LPS INSRT XXSM 12MM 05/31/2023
DEPUY IRELAND - 9616671 ATTUNE REV LPS INSRT XXSM 12MM 10/12/2022
DEPUY IRELAND - 9616671 ATTUNE REV LPS INSRT XSM 16MM 10/12/2022
DEPUY ORTHOPAEDICS INC US SROM NRHFEM W/PIN SM LFT 66X62 09/10/2022
ONKOS SURGICAL ELEOS 12/15/2021
-
-