Lensar, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories1
Latest FDA decision2022-06-09
SEC Filings: 1 filings on record. Latest: 10-Q (2026-08-13). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K220259 | ALLY Adaptive Cataract Treatment System | OOE | 2022-06-09 | View |
| 510(k) | K182795 | LENSAR Laser System - fs 3D (LLS-fs 3D) | OOE | 2018-12-21 | View |
| 510(k) | K181430 | LENSAR Laser System - fs 3D (LLS-fs 3D) | OOE | 2018-08-09 | View |
| 510(k) | K173346 | LENSAR Laser System - fs 3D (LLS-fs 3D) | OOE | 2018-03-02 | View |
| 510(k) | K171337 | LENSAR Laser System – fs 3D (LLS-fs 3D) | OOE | 2017-08-10 | View |
| 510(k) | K170576 | LENSAR Laser System - fs 3D (LLS-fs 3D) | OOE | 2017-05-05 | View |
No matching devices.