MAUDE Adverse Event Report: RxSight, Inc. Light Adjustable Lens (LAL)

Model Number	60005
Medical Device Problem Code	Patient Device Interaction Problem (4001)
Health Effect - Clinical Code	Unspecified Eye / Vision Problem (4471)
Date of Event	06/04/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
A site reported to rxsight that temporal zonular dehiscence was noted during implantation of a light adjustable lens (lal).The implanting surgeon reported that the zonular dehiscence precluded successful implantation of the lal because the lens could not be rotated.The surgeon completed the surgery, leaving the trailing haptic in the sulcus, and the optic and leading haptic within the capsular bag.Postoperatively, the patient was referred to a retinal surgeon.A secondary surgical procedure was subsequently performed to explant the dislocated lal and implant a non-rxsight intraocular lens (iol) via scleral fixation.A surgical peripheral iridotomy was also performed during the procedure.No additional information is available.
Additional Manufacturer Narrative
Manufacturing records were reviewed and found no deviations, non-conformances, or other manufacturing issues related to the reported event.Manufacturer reference #: (b)(4).

• Brand Name: Light Adjustable Lens (LAL)
• Common Device Name: Light Adjustable Lens (LAL)
• Manufacturer (Section D): RxSight, Inc.; 100 columbia; aliso viejo CA 92656
• Manufacturer (Section G): RxSight, Inc.; 100 columbia; aliso viejo CA 92656
• Manufacturer Contact: jim zhang ; 100 columbia; aliso viejo, CA 92656 ; +1(949)273-6163
• MDR Report Key: 50046886
• Report Number: 3012712027-2026-00341
• Device Sequence Number: 9490833
• Product Code: PZK
• UDI-Device Identifier: 00818806020586
• UDI-Public: (01)00818806020586(11)250223(17)280131
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: P160055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2026
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 07/27/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 60005
• Device Catalogue Number: 60005
• Device Lot Number: L07-008261
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/02/2026
• Initial Report FDA Received Date: 07/27/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 02/23/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 39 YR
• Patient Sex: Female