Atlas FDA

Light Adjustable Lens, Light Delivery System

FDA premarket approval P160055/S046 · decided 2025-06-11

Approval details

PMA number
P160055
Supplement
S046
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Light Adjustable Lens, Light Delivery System
Generic name
Light adjustable lens (LAL) and light delivery device (LDD)
Applicant
Rxsight, Inc.
Date received
2025-03-17
Decision date
2025-06-11
Days to decision
86 days
Decision code
APPR
Product code
PZK
Advisory committee
Ophthalmic
Expedited review
No
Location
Aliso Viejo, CA
Statement
approval for minor design modifications of an optical assembly inside the Light Delivery Device Model 61002-007

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510(k) clearances by this applicant

RecordFirmDate
RxSight® Insertion Device (K261174)Rxsight, Inc.2026-06-10
RxSight® Insertion Device (63002) (K231838)Rxsight, Inc.2023-08-15
RxSight Insertion Device (K231466)Rxsight, Inc.2023-06-12
RxSight Contact Lens (K201909)Rxsight, Inc.2020-09-10
RxSight Insertion Device (K192926)Rxsight, Inc.2020-01-17
RxSight Insertion Device (K181401)Rxsight, Inc.2018-07-26