• 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 
 > 
 
29 records meeting your search criteria returned- Product Code: LMH Patient Problem: Unspecified Vascular Problem Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TEOXANE SA NA 04/28/2022
TEOXANE SA NA 04/25/2022
Q-MED RESTYLANE CONTOUR 02/28/2022
Q-MED RESTYLANE CONTOUR 02/28/2022
TEOXANE SA TEOSYAL RHA 1 02/24/2022
TEOXANE SA TEOSYAL RHA 4 11/22/2021
TEOXANE SA TEOSYAL RHA 4 09/28/2021
MERZ NORTH AMERICA INC RADIESSE INJECTABLE IMPLANT 07/14/2021
TEOXANE SA TEOSYAL RHA 2 07/09/2021
TEOXANE SA TEOSYAL RHA 3 07/05/2021
-
-