FDA 510(k) Applications Submitted by LENSAR, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K220259 01/31/2022 ALLY Adaptive Cataract Treatment System Lensar, Inc.
K170576 02/27/2017 LENSAR Laser System - fs 3D (LLS-fs 3D) LENSAR, Inc.
K171337 05/08/2017 LENSAR Laser System û fs 3D (LLS-fs 3D) LENSAR, Inc.
K181430 06/01/2018 LENSAR Laser System - fs 3D (LLS-fs 3D) LENSAR, Inc.
K182795 10/01/2018 LENSAR Laser System - fs 3D (LLS-fs 3D) Lensar, Inc.
K173346 10/25/2017 LENSAR Laser System - fs 3D (LLS-fs 3D) Lensar, Inc.
K152453 08/28/2015 LENSAR Laser System - fs 3D (LLS-fs 3D) LENSAR, Inc.
K143010 10/20/2014 LENSAR Laser System - fs 3D LENSAR, INC.
K120214 01/24/2012 TBD LENSAR, INC.
K090633 03/09/2009 LENSAR LASER SYSTEM LENSAR, INC.
K112098 07/22/2011 TBD LENSAR, INC.
K102727 09/22/2010 LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMY LENSAR, INC.
K122829 09/17/2012 LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS LENSAR, INC.
K123859 12/14/2012 TBD LENSAR, INC.


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