Medical Device Manufacturer · US , Winter Park , FL

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

14 submissions · 14 cleared · Since 2010

Total

Cleared

Denied

Lensar, Inc. has 14 FDA 510(k) cleared ophthalmic devices. Based in Winter Park, US.

Last cleared in 2022. Active since 2010.

Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.

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

14 devices

1-12 of 14

Cleared Jun 09, 2022

ALLY Adaptive Cataract Treatment System

K220259 · OOE

Ophthalmic · 129d

Cleared Dec 21, 2018

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

K182795 · OOE

Ophthalmic · 81d

Cleared Aug 09, 2018

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

K181430 · OOE

Ophthalmic · 69d

Cleared Mar 02, 2018

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

K173346 · OOE

Ophthalmic · 128d

Cleared Aug 10, 2017

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

K171337 · OOE

Ophthalmic · 94d

Cleared May 05, 2017

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

K170576 · OOE

Ophthalmic · 67d

Cleared Oct 15, 2015

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

K152453 · OOE

Ophthalmic · 48d

Cleared Mar 20, 2015

LENSAR Laser System - fs 3D

LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS

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

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

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