• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
308 records meeting your search criteria returned- Product Code: HQL Patient Problem: Vitrectomy Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
JOHNSON & JOHNSON SURGICAL VISION, INC. TECNIS CL 03/26/2020
JOHNSON & JOHNSON SURGICAL VISION, INC. SENSAR 03/26/2020
ALCON RESEARCH, LLC - HUNTINGTON ACRYSOF IQ NATURAL SINGLEPIECE IOL 03/20/2020
JOHNSON & JOHNSON SURGICAL VISION, INC. TECNIS 03/18/2020
JOHNSON & JOHNSON SURGICAL VISION, INC. TECNIS 03/18/2020
BAUSCH + LOMB ENVISTA INTRAOCULAR LENS 03/13/2020
HOYA SURGICAL OPTICS, INC. HOYA ISERT 250 03/11/2020
JOHNSON & JOHNSON SURGICAL VISION, INC. TECNIS ITEC PRELOADED 1-PIECE IOL 03/10/2020
JOHNSON & JOHNSON SURGICAL VISION, INC. SENSAR 03/09/2020
JOHNSON & JOHNSON SURGICAL VISION, INC. SENSAR 03/09/2020
-
-