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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.
Generic NameLight adjustable lens (LAL) and light delivery device (LDD)
Regulation Number886.3600
ApplicantRxSight, Inc.
100 Columbia
Aliso Viejo, CA 92656
PMA NumberP160055
Date Received12/09/2016
Decision Date11/22/2017
Product Code PZK 
Docket Number 17M-6614
Notice Date 12/05/2017
Advisory Committee Ophthalmic
Clinical TrialsNCT00845520
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Approval for The Light Adjustable Lens and Light Delivery Device system is indicated for the reduction residual astigmatism to improve uncorrected visual acuity after removal of the cataractous natural lens by phacoemulsification and implantation of the intraocular lens in the capsular bag, in adult patients: 1) With pre-existing corneal astigmatism of => 0.75 diopters; and 2) Without pre-existing macular disease. The system also reduces the likelihood of clinically significant residual spherical refractive errors.
Approval OrderApproval Order
SummarySummary of Safety and Effectiveness
Labeling Part 2
Post-Approval StudyShow Report Schedule and Study Progress
Supplements:  S002 S003 S004 S005 S006 S007 S008 S009 S010 S011 S014 
S015 S016 S017 S018 S019 S021 S022 S023 S024 S025 S026 S027 
S028 S029 S031 S032 S033