Rxsight, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories3
Latest FDA decision2026-06-26
SEC Filings: 1 filings on record. Latest: 10-Q (2026-08-05). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P160055 | Light adjustable lens (LAL) and light delivery device (LDD) | PZK | 2026-06-26 | View |
| 510(k) | K261174 | RxSight® Insertion Device | MSS | 2026-06-10 | View |
| 510(k) | K231838 | RxSight® Insertion Device (63002) | MSS | 2023-08-15 | View |
| 510(k) | K231466 | RxSight Insertion Device | MSS | 2023-06-12 | View |
| 510(k) | K201909 | RxSight Contact Lens | HJK | 2020-09-10 | View |
| 510(k) | K192926 | RxSight Insertion Device | MSS | 2020-01-17 | View |
| 510(k) | K181401 | RxSight Insertion Device | MSS | 2018-07-26 | View |
No matching devices.