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Lensar, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220259ALLY Adaptive Cataract Treatment SystemJune 9, 2022
K182795LENSAR Laser System - fs 3D (LLS-fs 3D)December 21, 2018
K181430LENSAR Laser System - fs 3D (LLS-fs 3D)August 9, 2018
K173346LENSAR Laser System - fs 3D (LLS-fs 3D)March 2, 2018
K171337LENSAR Laser System – fs 3D (LLS-fs 3D)August 10, 2017
K170576LENSAR Laser System - fs 3D (LLS-fs 3D)May 5, 2017
K152453LENSAR Laser System - fs 3D (LLS-fs 3D)October 15, 2015
K143010LENSAR Laser System - fs 3DMarch 20, 2015
K123859TBDMarch 27, 2013
K122829LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONSDecember 3, 2012
K120214TBDJune 8, 2012
K112098TBDOctober 19, 2011
K102727LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMYMarch 16, 2011
K090633LENSAR LASER SYSTEMMay 13, 2010