• 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 
 > 
 
29 records meeting your search criteria returned- Product Code: EMA Patient Problem: Hypersensitivity/Allergic reaction Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GC CORP. FUJI IX GP 01/10/2024
DENTSPLY LLC CALIBRA VEN TRY-IN 1.8GM MD RF 06/23/2023
DENTSPLY LLC CALIBRA VEN TRY-IN 1.8GM LT RF 06/23/2023
DENTSPLY LLC INTEGRITY TEMP GRIP REFILL PK 03/09/2023
DENTSPLY LLC CALIBRA UNIV CEM SYR REF TRAN 02/28/2022
DENTSPLY DETREY GMBH CHEMFIL SUP. EXP. REF. L 10/27/2021
Unknown Manufacturer IRM CAPS ENCAPSULATED ZOE INTERNEDIATE R 02/18/2021
DENTSPLY CAULK IRM ZOE INTERMEDIATE RESTORATIVE MATERIA 01/06/2021
DENTSPLY CAULK CALIBRA 11/21/2020
DENTSPLY DETREY GMBH IRM CEMENT 06/22/2020
-
-