Medical Device Manufacturer · US , Winter Park , FL

Lensar, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 2010

14

Total

14

Cleared

0

Denied

FDA 510(k) cleared devices by Lensar, Inc. Ophthalmic ✕

14 devices

1-12 of 14

Cleared Jun 09, 2022

ALLY Adaptive Cataract Treatment System

Ophthalmic · 129d

Cleared Dec 21, 2018

LENSAR Laser System - fs 3D (LLS-fs 3D)

Ophthalmic · 81d

Cleared Aug 09, 2018

LENSAR Laser System - fs 3D (LLS-fs 3D)

Ophthalmic · 69d

Cleared Mar 02, 2018

LENSAR Laser System - fs 3D (LLS-fs 3D)

Ophthalmic · 128d

Cleared Aug 10, 2017

LENSAR Laser System – fs 3D (LLS-fs 3D)

Ophthalmic · 94d

Cleared May 05, 2017

LENSAR Laser System - fs 3D (LLS-fs 3D)

Ophthalmic · 67d

Cleared Oct 15, 2015

LENSAR Laser System - fs 3D (LLS-fs 3D)

Ophthalmic · 48d

Cleared Mar 20, 2015

LENSAR Laser System - fs 3D

Ophthalmic · 151d

Cleared Mar 27, 2013

Ophthalmic · 103d

Cleared Dec 03, 2012

LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS

Ophthalmic · 77d

Cleared Jun 08, 2012

Ophthalmic · 136d

Cleared Oct 19, 2011

Ophthalmic · 89d