• 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 
 > 
 
58 records meeting your search criteria returned- Product Code: NKB Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH UNK - RODS: MATRIX 03/25/2024
GLOBUS MEDICAL, INC. CREO 03/04/2024
SYNTHES GMBH UNK - SCREWS: ZERO-P 12/29/2023
SYNTHES GMBH UNK - RODS: TROLLY 07/21/2023
SYNTHES GMBH UNK - TROLLEY SCREWS 07/21/2023
SYNTHES GMBH UNK - SCREWS: SPINE-US 06/01/2023
NUVASIVE, INCORPORATED NUVASIVE® PRECEPT¿ SPINAL SYSTEM 10/26/2022
SYNTHES GMBH UNK - CONSTRUCTS: MATRIX 10/17/2022
SYNTHES GMBH UNK - SCREWS: ZERO-P 07/29/2022
MEDACTA INTERNATIONAL SA PEDICLE SCREW MUST MC SCREW Ø6X40 REDUCT 04/05/2022
-
-