• 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 
 4 
 5 
 6 
 > 
 
57 records meeting your search criteria returned- Product Code: HSB Patient Problem: Irritation Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER TRAUMA KIEL RECONSTRUCTION NAIL R2.0, TI, LEFT T2 RE 07/23/2018
STRYKER TRAUMA KIEL UNK T2 RECON DISTAL LOCKING SCREW 07/23/2018
STRYKER TRAUMA KIEL UNK DISTAL SCREW 07/12/2018
STRYKER TRAUMA KIEL UNK DISTAL INTERLOCKING SCREW 07/10/2018
STRYKER TRAUMA KIEL UNK T2 TIBIA NAIL 07/10/2018
STRYKER TRAUMA KIEL UNK DISTAL INTERLOCKING SCREW 07/10/2018
STRYKER TRAUMA KIEL UNK T2 TIBIA NAIL 07/10/2018
STRYKER TRAUMA KIEL UNK T2 DTM DISTAL INTERLOCKING SCREW 07/02/2018
ACUMED LLC ROD, FIXATION, INTRAMEDULLARY AND ACCESS 05/18/2018
ACUMED LLC ROD, FIXATION, INTRAMEDULLARY AND ACCESS 05/18/2018
-
-