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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
348 records meeting your search criteria returned- Product Code: LPH Patient Problem: Ossification Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 01/31/2023
DEPUY ORTHOPAEDICS INC US ALTRX +4 10D 32IDX48OD 01/26/2023
DEPUY ORTHOPAEDICS INC US ALTRX NEUT 32IDX48OD 01/09/2023
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR LINERS 12/09/2022
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR CUP 12/09/2022
DEPUY IRELAND - 9616671 UNK HIP FEMORAL STEM CORAIL 12/09/2022
ZIMMER BIOMET, INC. G7 VIT E NEUTRAL LNR 36MM F 11/14/2022
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ6 HI OFF 10/20/2022
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 50MM 10/13/2022
DEPUY ORTHOPAEDICS INC US ALTRX NEUT 32IDX50OD 10/13/2022
-
-