FDA.reportPublic FDA data

LENSAR, Inc

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30090260573009026057LENSAR, Inc1N2026-01-012800 Discovery Drive Suite 100 Orlando FL US 32826

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1424391810852651K220259ALLY Adaptive Cataract Treatment SystemOOE2022-06-09
1424391744869885K182795LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2018-12-21
1424391930104938K181430LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2018-08-09
1424391407090801K173346LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2018-03-02
1424391934647349K171337LENSAR Laser System – fs 3D (LLS-fs 3D)OOE2017-08-10
1424391427786764K170576LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2017-05-05
1424391478616018K152453LENSAR Laser System - fs 3D (LLS-fs 3D)OOE2015-10-15
1424391659595458K143010LENSAR Laser System - fs 3DOOE2015-03-20
1424391793118399K123859TBDOOE2013-03-27
1424391961538724K122829LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONSHQC2012-12-03
1424391984838471K120214TBDOOE2012-06-08
1424391329890354K112098TBDOOE2011-10-19
1424392030202284K102727LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMYOOE2011-03-16
1424391756759548K090633LENSAR LASER SYSTEMOOE2010-05-13

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OOE132022-06-09
HQC12012-12-03