Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list RxSight with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 10, 2026: RxSight® Insertion Device.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jun 10, 2026 | RxSight® Insertion DeviceK261174 · MSS | 510(k) clearances |
| Aug 15, 2023 | RxSight® Insertion Device (63002)K231838 · MSS | 510(k) clearances |
| Jun 12, 2023 | RxSight Insertion DeviceK231466 · MSS | 510(k) clearances |
| Sep 10, 2020 | RxSight Contact LensK201909 · HJK | 510(k) clearances |
| Jan 17, 2020 | RxSight Insertion DeviceK192926 · MSS | 510(k) clearances |
| Jul 26, 2018 | RxSight Insertion DeviceK181401 · MSS | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
