Lensar, Inc.
Lensar, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2022.
Top product codes for Lensar, Inc.
Recent clearances by Lensar, Inc.
- K220259 — ALLY Adaptive Cataract Treatment System
- K182795 — LENSAR Laser System - fs 3D (LLS-fs 3D)
- K181430 — LENSAR Laser System - fs 3D (LLS-fs 3D)
- K173346 — LENSAR Laser System - fs 3D (LLS-fs 3D)
- K171337 — LENSAR Laser System fs 3D (LLS-fs 3D)
- K170576 — LENSAR Laser System - fs 3D (LLS-fs 3D)
- K152453 — LENSAR Laser System - fs 3D (LLS-fs 3D)
- K143010 — LENSAR Laser System - fs 3D
- K123859 — TBD
- K122829 — LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS
- K120214 — TBD
- K112098 — TBD
- K102727 — LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMY
- K090633 — LENSAR LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.