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

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) Regulatory Record - Lensar, Inc.
14 devices
1-14 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
K143010 · OOE
Ophthalmic · 151d
Cleared Mar 27, 2013
TBD
K123859 · OOE
Ophthalmic · 103d
Cleared Dec 03, 2012
LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS
K122829 · HQC
Ophthalmic · 77d
Cleared Jun 08, 2012
TBD
K120214 · OOE
Ophthalmic · 136d
Cleared Oct 19, 2011
TBD
K112098 · OOE
Ophthalmic · 89d
Cleared Mar 16, 2011
LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMY
K102727 · OOE
Ophthalmic · 175d
Cleared May 13, 2010
LENSAR LASER SYSTEM
K090633 · OOE
Ophthalmic · 430d
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