• 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 
 > 
 
130 records meeting your search criteria returned- Product Code: MOZ Patient Problem: Rash Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GENZYME CORPORATION SYNVISC 11/09/2020
GENZYME CORPORATION SYNVISC HYLAN G-F 20 11/09/2020
GENZYME CORPORATION SYNVISC HYLAN G-F 20 11/06/2020
GENZYME CORPORATION(RIDGEFIELD) SYNVISC 10/29/2020
SEIKAGAKU CORPORATION ARTZ DISPO 08/18/2020
SEIKAGAKU CORPORATION, TAKAHAGI PLANT GELONE SYRINGE 06/17/2020
GENZYME CORPORATION(RIDGEFIELD) SYNVISC 05/26/2020
Q-MED AB DUROLANE 05/08/2020
GALDERMA Q-MED AB DUROLANE 03/30/2020
SEIKAGAKU CORPORATION GEL-ONE 03/12/2020
-
-