• 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 
 7 
 8 
 9 
 10 
 > 
 
182 records meeting your search criteria returned- Product Code: LZS Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
Unknown Manufacturer LASER 03/15/2022
Unknown Manufacturer FEMTOLASIK 10/26/2021
Unknown Manufacturer EYE LASER 09/07/2021
Unknown Manufacturer LASIK 07/07/2021
Unknown Manufacturer EXCIMER LASER 04/12/2021
WAVELIGHT GMBH ALLEGRETTO WAVE EYE-Q EXCIMER LASER 12/24/2020
WAVELIGHT GMBH WAVELIGHT EX500 EXCIMER LASER 12/21/2020
CARL ZEISS MEDITEC AG (JENA) MEL80 EXCIMER LASER SYSTEM 08/12/2020
UNKNOWN PRK LASIK 07/14/2020
WAVELIGHT GMBH WAVELIGHT EX500 EXCIMER LASER 05/22/2020
-
-