• 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 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
124 records meeting your search criteria returned- Product Code: NKB Patient Problem: Foreign Body In Patient Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDOS INTERNATIONAL SàRL CH VIPER PRIME CFXFEN XTAB 7X50MM 07/20/2020
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 07/15/2020
ULRICH MEDICAL USA MOMENTUM 07/15/2020
ZIMMER SPINE FINAL SCREWDRIVER SHAFT II 07/07/2020
ZIMMER SPINE FINAL SCREWDRIVER SHAFT II 07/06/2020
ZIMMER BIOMET SPINE INC. 5.5 HA MULTI SCREW 7.5 X 40MM 06/11/2020
MEDOS INTERNATIONAL SàRL CH EXP TI POLY SCREW 11MMX80MM 06/02/2020
MEDOS INTERNATIONAL SàRL CH VIPER PRIME STYLET 05/21/2020
ZIMMER BIOMET SPINE INC. CANNULATED POLYAXIAL EXTENDED TAB SCREW 04/28/2020
ZIMMER BIOMET SPINE INC. K-WIRE TROCAR, THREADED 04/28/2020
-
-