Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 
8 records meeting your search criteria returned- Product Code: LWJ Product Problem: Loosening of Implant Not Related to Bone-Ingrowth Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG METHA ¿CAP 12/14 130°/0° SIZE 0 07/20/2023
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STEM 09/12/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 02/07/2022
AESCULAP AG ISODUR PROSTHESIS HEAD 8/10 28MM L 12/06/2021
MICROPORT ORTHOPEDICS INC. PROFEMUR MODULAR FEMORAL NECK 03/06/2020
AESCULAP AG BIOLOX PROSTHESIS HEAD 12/14 28MM S 09/20/2019
SMITH & NEPHEW ORTHOPAEDICS AG SL-PLUS STANDARD STEM 7 NON-CEMENTED 11/14/2018
ENCORE MEDICAL L.P. LIMA HIP 10/05/2018
-
-