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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