• 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 
 8 
 9 
 10 
 > 
 
112 records meeting your search criteria returned- Product Code: NPJ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAKO SURGICAL CORP. MAKO UKR X3 ONLAY INSERT SIZE 4 - 8 MM 03/29/2024
MAKO SURGICAL CORP. UNKNOWN_MAKO ROBOTIC ARM ASSISTED UKA 03/28/2024
DEPUY ORTHOPAEDICS INC US SIGMA HP UNI A/P SZ2 8MM RMLL 03/20/2024
DEPUY ORTHOPAEDICS INC US SIGMA HP UNI FEMORAL SZ2 RM/LL 03/18/2024
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 4-8MM 01/23/2024
MAKO SURGICAL CORP. MAKO UKR X3 ONLAY INSERT SIZE 3 - 8 MM 11/14/2023
MAKO SURGICAL CORP. MAKO UKR X3 ONLAY INSERT SIZE 3 - 8 MM 11/04/2023
MAKO SURGICAL CORP. UNKNOWN_SZ 5 LEFT MCK PATELLOFEMORAL 11/02/2023
CONFORMIS, INC IDUO PKRS 11/01/2023
MAKO SURGICAL CORP. MCK TIBIAL BASEPLATE-RM/LL-SZ 3 10/24/2023
-
-