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

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
 

 
 
6 records meeting your search criteria returned- Product Code: HRY Patient Problem: Implant Pain Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIMACORPORATE S.P.A. PHYSICA FIXED TIBIAL PLATE #3 02/13/2023
AESCULAP AG AS UNIVATION XF TIBIA CEMENTED T1 LM 07/08/2021
SMITH & NEPHEW, INC. UNKN JOURNEY BCS / JOURNEY II BCS KNEE F 06/24/2021
AESCULAP AG UNIVATION XF TIBIA ZEMENTIERT T4 LM 02/25/2021
AESCULAP AG COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN 07/10/2020
AESCULAP AG COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN 07/10/2020
-
-