• 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
 

 
 
5 records meeting your search criteria returned- Product Code: OOK Patient Problem: Emotional Changes Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZELTIQ AESTHETICS INC. COOLSCULPTING 04/25/2023
ZELTIQ AESTHETICS, INC. COOLSCULPTING 08/18/2022
ZELITIQ AESTHETICS, INC COOLSCULPTING 07/19/2022
ALLERGAN/ABBVIE IRELAND NL B.V. BALLYTIV COOLSCULPTING 07/19/2022
ALLERGAN (PLEASANTON) COOLSCULPTING SYSTEM 06/08/2021
-
-