• 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 
 > 
 
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
ARJOHUNTLEIGH POLSKA SP. Z O.O. CITADEL PLUS 12/13/2022
HILL-ROM BATESVILLE CENTRELLA MED-SURG 12/12/2022
HILL-ROM BATESVILLE VERSACARE FRAME 12/12/2022
JOERNS HEALTHCARE WECARE 12/12/2022
ARJOHUNTLEIGH POLSKA SP. Z O.O. ENTERPRISE 8000X 12/12/2022
HILL-ROM BATESVILLE PROGRESSA FRAME 12/09/2022
HILL-ROM BATESVILLE VERSACARE FRAME 12/08/2022
ARJOHUNTLEIGH POLSKA SP. Z O.O. CITADEL PLUS 12/07/2022
JOERNS HEALTHCARE WECARE BED 12/06/2022
UMANO MEDICAL INC. OOK SNOW 12/06/2022
-
-