• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
312 records meeting your search criteria returned- Product Code: LPH Patient Problem: Muscle/Tendon Damage Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER ORTHOPAEDICS-MAHWAH TRIDENTII TRITANIUM CLUSTER52E 11/20/2023
STRYKER ORTHOPAEDICS-MAHWAH TRIDENT X3 ELEVATED RIM 36MM ID 11/20/2023
ZIMMER MANUFACTURING B.V. FEMORAL HEAD STERILE PRODUCT DO NOT REST 10/10/2023
ZIMMER BIOMET, INC. UNK SIZE 7 ALLOCLASSIC HIGH OFFSET STEMS 10/06/2023
ZIMMER BIOMET, INC. UNK 38MM CROSS-LINKED DURASUL POLYETHYLE 10/06/2023
ZIMMER BIOMET, INC. UNK HEAD 38MM +4 COBALT-CHROME HEAD 10/06/2023
ZIMMER BIOMET, INC. FEMORAL HEAD STERILE PRODUCT DO NOT REST 08/31/2023
ZIMMER MANUFACTURING B.V. BONE SCREW SELF-TAPPING 6.5 MM DIA. 35 M 08/31/2023
ZIMMER BIOMET, INC. MODULAR NECK B 12/14 NECK TAPER USE WITH 08/31/2023
ZIMMER MANUFACTURING B.V. FEMORAL HEAD STERILE PRODUCT DO NOT REST 08/31/2023
-
-