510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K122829Substantially Equivalent

Lensar Laser System - Fs 3D for Corneal Incisions

LENSAR, Inc, Orlando FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K122829 is the FDA 510(k) clearance record for LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS, a class II device, cleared for Lensar, Inc. on under FDA product code HQC (Unit, Phacofragmentation). FDA records list 14 510(k) clearances for Lensar, Inc., from to . As of , FDA records show no recalls naming K122829.

Clearance record

Decision date
Received
(77 days to decision)
Product code
HQC Unit, Phacofragmentation
Regulation
21 CFR 886.4670
Device class
Class II
Review panel
Ophthalmic
Applicant
Lensar, Inc. 2800 Discovery Dr., Suite 100, Orlando FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HQC

Trailing 12 months
3 clearances under product code HQC in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HQC, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260