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Lensar, Inc.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K220259 ALLY Adaptive Cataract Treatment SystemOOE2022-06-09 View
510(k) K182795 LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2018-12-21 View
510(k) K181430 LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2018-08-09 View
510(k) K173346 LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2018-03-02 View
510(k) K171337 LENSAR Laser System – fs 3D (LLS-fs 3D)OOE2017-08-10 View
510(k) K170576 LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2017-05-05 View
510(k) K123859 TBDOOE2013-03-27 View
510(k) K122829 LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONSHQC2012-12-03 View
510(k) K120214 TBDOOE2012-06-08 View
510(k) K112098 TBDOOE2011-10-19 View
510(k) K102727 LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMYOOE2011-03-16 View
510(k) K090633 LENSAR LASER SYSTEMOOE2010-05-13 View
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