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

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
 

 
 
7 records meeting your search criteria returned- Product Code: LQE Patient Problem: Pain Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
REVISION OPTICS/RVO 2.0 INC. RAINDROP INLAY 01/22/2020
RVO 2.0, INC. RAINDROP INLAY 03/29/2019
REVISION OPTICS RAINDROP NEAR VISION INLAY 06/22/2017
REVISION OPTICS RAINDROP NEAR VISION INLAY 01/17/2017
ACUFOCUS, INC. KAMRA INLAY 11/10/2016
ACUFOCUS ACUFOCUS 10/26/2016
ACUFOCUS, INC. KAMRA 03/18/2016
-
-