• 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 
 > 
 
23 records meeting your search criteria returned- Product Code: MRA Patient Problem: Loss of Range of Motion Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US DELTA CER INSERT 32ID X 48OD 10/12/2022
MICROPORT ORTHOPEDICS INC. UNKNOWN PROFEMUR STEM 04/27/2022
SMITH & NEPHEW ORTHOPAEDICS LTD UNKNOWN BIRMINGHAM HIP RESURFACING (BHR) 09/28/2021
DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT36IDX58OD 08/26/2021
DEPUY ORTHOPAEDICS INC US CERAMAX CERAMIC INSERT 36 X 54 05/17/2021
SMITH & NEPHEW, INC. R3 3 HOLE ACET SHELL 52MM 02/26/2021
MICROPORT ORTHOPEDICS INC. LINEAGE TRANSCEND CERAMIC ACETABULAR LIN 12/02/2020
MICROPORT ORTHOPEDICS INC. CERAMIC FEMORAL HEAD 12/02/2020
SMITH & NEPHEW, INC. UNKN R3 CERAMIC LINER 07/23/2020
MICROPORT ORTHOPEDICS INC. LINEAGE TRANSCEND CERAMIC ACETABULAR LIN 03/10/2020
-
-