Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
17 records meeting your search criteria returned- Product Code: NLQ Product Problem: Fracture Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER-ENDOSCOPY LAKELAND 5300 NA 02/20/2024
STRYKER-ENDOSCOPY LAKELAND 5300 NA 01/19/2024
STRYKER-ENDOSCOPY LAKELAND 5300 NA 08/03/2023
STRYKER-ENDOSCOPY LAKELAND 5300 NA 06/21/2023
STRYKER-ENDOSCOPY LAKELAND 5300 NA 05/23/2023
STRYKER-ENDOSCOPY LAKELAND 5300 NA 05/09/2023
STRYKER-ENDOSCOPY LAKELAND 5300 NA 04/04/2023
STRYKER SUSTAINABILITY SOLUTIONS LAKELAN NA 12/01/2022
STRYKER SUSTAINABILITY SOLUTIONS LAKELAN NA 11/23/2022
STRYKER SUSTAINABILITY SOLUTIONS LAKELAN NA 04/04/2022
-
-