• 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 
 14 
 > 
 
344 records meeting your search criteria returned- Product Code: NKB Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SEASPINE, INC MARINER DEFORMITY 11/04/2021
ULRICH GMBH & CO. KG UCENTUM 11/03/2021
ULRICH GMBH & CO. KG UCENTUM 11/03/2021
ZIMMER BIOMET SPINE INC. BOTTOM LOADING POLY OPEN ILIAC SCREW ASS 11/03/2021
SEASPINE, INC MARINER MIS 10/29/2021
STRYKER SPINE-US 7.5X80 MEDIAL BIASED ANGLE POLYAXIAL SCR 10/05/2021
STRYKER SPINE-US 7.5X80 MEDIAL BIASED ANGLE POLYAXIAL SCR 10/05/2021
ZIMMER BIOMET SPINE INC. CANNULATED POLYAXIAL SCREW 6.5MM X 45MM 10/04/2021
ZIMMER BIOMET SPINE INC. CANNULATED POLYAXIAL SCREW 6.5MM X 45MM 10/04/2021
ZIMMER BIOMET SPINE INC. CANNULATED POLYAXIAL SCREW 6.5MM X 45MM 09/28/2021
-
-