FDA 510(k) Applications Submitted by RxSight, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231466 | 05/19/2023 | RxSight Insertion Device | RxSight, Inc. |
| K181401 | 05/29/2018 | RxSight Insertion Device | RxSight, Inc. |
| K201909 | 07/09/2020 | RxSight Contact Lens | RxSight, Inc. |
| K192926 | 10/16/2019 | RxSight Insertion Device | RxSight, Inc. |
| K231838 | 06/22/2023 | RxSight« Insertion Device (63002) | RxSight, Inc. |
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