• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • 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

New Search Back to Search Results
DeviceCustomFlex Artificial Iris
Classification Nameartificial iris
Generic Nameartificial iris
Clinical Research Consultants, Inc.
3308 jefferson avenue, upper level
cincinnati, OH 45220
PMA NumberP170039
Date Received11/29/2017
Decision Date05/30/2018
Product Code
QBT[ Registered Establishments with QBT ]
Advisory Committee Ophthalmic
Clinical Trials NCT01860612
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the CustomFlex Artificial Iris. The CustomFlex Artificial Iris is indicated for use in children and adults for the treatment of full or partial aniridia resulting from congenital aniridia, acquired defects, or other conditions associated with full or partial aniridia.
Approval Order Approval Order
Summary Summary of Safety and Effectiveness
Labeling Labeling
Labeling Part 2
Post-Approval StudyShow Report Schedule and Study Progress