• 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 
 > 
 
18 records meeting your search criteria returned- Product Code: HTD Patient Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH RONG CURV 6 BLACK 04/29/2024
SYNTHES GMBH REDUCTION FORCEPS POINTS BROAD-RATCHET 04/25/2024
SYNTHES GMBH SLIDING MECHANISM 04/09/2024
SYNTHES GMBH PERCUTANEOUS ARM 255MM 04/09/2024
SYNTHES GMBH REDUCTION FORCEPS WITH SERRATED JAW-RATC 03/11/2024
SYNTHES GMBH PELVIC ARM 225MM 03/04/2024
SYNTHES GMBH SLIDING MECHANISM 02/16/2024
SYNTHES GMBH REDUCTION FORCEPS WITH SERRATED JAW-RATC 02/05/2024
SYNTHES GMBH RED FORCEPS SERRATED JAW-RATCHET 144 01/30/2024
SYNTHES GMBH SLIDING MECHANISM 01/18/2024
-
-