• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENCORE MEDICAL L.P. RSP 05/18/2022
ENCORE MEDICAL L.P. RSP 05/18/2022
ENCORE MEDICAL L.P RSP 05/18/2022
ENCORE MEDICAL L.P RSP 05/18/2022
ENCORE MEDICAL L.P. RSP 05/16/2022
ENCORE MEDICAL L.P RSP 05/16/2022
ENCORE MEDICAL L.P. RSP 05/14/2022
ENCORE MEDICAL L.P RSP 05/14/2022
MEDACTA INTERNATIONAL SA REVERSE SHOULDER SYSTEM HUMERAL REVERSE 05/13/2022
MEDACTA INTERNATIONAL SA HUMERAL REVERSE HC LINER Ø39/+0MM 05/12/2022
-
-