# Rxsight, Inc.

- Location (FDA's records): Aliso Viejo, CA
- FDA decisions: 7 (2017–2026): 6 510(k) clearances and 1 original PMA approval
- Product codes: MSS (5), HJK (1), PZK (1)
- Predicates its devices cite: 9 (5 its own); citations of its devices by later devices: 5 (5 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ast Products, Inc.: 2 (https://510kreport.com/company/ast-products)
- Bausch & Lomb, Inc.: 1 (https://510kreport.com/company/bausch-lomb)
- Ocular Instruments, Inc.: 1 (https://510kreport.com/company/ocular-instruments)

## Its most-cited devices
- K231466: RxSight Insertion Device (2023), cited by 2
- K231838: RxSight® Insertion Device (63002) (2023), cited by 1
- K192926: RxSight Insertion Device (2020), cited by 1
- K181401: RxSight Insertion Device (2018), cited by 1

## Recent decisions
- K261174: RxSight® Insertion Device (Jun 10, 2026)
- K231838: RxSight® Insertion Device (63002) (Aug 15, 2023)
- K231466: RxSight Insertion Device (Jun 12, 2023)
- K201909: RxSight Contact Lens (Sep 10, 2020)
- K192926: RxSight Insertion Device (Jan 17, 2020)
- K181401: RxSight Insertion Device (Jul 26, 2018)
- P160055: Light Adjustable Lens (Lal) and Light Delivery Device (LDD) (Nov 22, 2017)

Source page: https://510kreport.com/company/rxsight