ClearanceBrief
Company · US

Lensar, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2022. Name variants (Inc, Corp, punctuation) are merged.

14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OOEOphthalmic Femtosecond Laser13
HQCUnit, Phacofragmentation1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 9, 2022K220259ALLY Adaptive Cataract Treatment System
Lensar, Inc.
OOE
Dec 21, 2018K182795LENSAR Laser System - fs 3D (LLS-fs 3D)
Lensar, Inc.
OOE
Aug 9, 2018K181430LENSAR Laser System - fs 3D (LLS-fs 3D)
Lensar, Inc.
OOE
Mar 2, 2018K173346LENSAR Laser System - fs 3D (LLS-fs 3D)
Lensar, Inc.
OOE
Aug 10, 2017K171337LENSAR Laser System – fs 3D (LLS-fs 3D)
Lensar, Inc.
OOE
May 5, 2017K170576LENSAR Laser System - fs 3D (LLS-fs 3D)
Lensar, Inc.
OOE
Oct 15, 2015K152453LENSAR Laser System - fs 3D (LLS-fs 3D)
Lensar, Inc.
OOE
Mar 20, 2015K143010LENSAR Laser System - fs 3D
Lensar, Inc.
OOE
Mar 27, 2013K123859TBD
Lensar, Inc.
OOE
Dec 3, 2012K122829LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS
Lensar, Inc.
HQC
Jun 8, 2012K120214TBD
Lensar, Inc.
OOE
Oct 19, 2011K112098TBD
Lensar, Inc.
OOE
Mar 16, 2011K102727LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMY
Lensar, Inc.
OOE
May 13, 2010K090633LENSAR LASER SYSTEM
Lensar, Inc.
OOE

Latest recalls

DateFirm and productCodeLinked 510(k)
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