510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
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K900199Substantially Equivalent

Lasag Microrupter 2 Nd:yag Laser Trabeculoplasty

Lasag AG, Claremont CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900199 is the FDA 510(k) clearance record for LASAG MICRORUPTER 2 ND:YAG LASER TRABECULOPLASTY, a class II device, cleared for Lasag AG on under FDA product code HQF (Laser, Ophthalmic). FDA records list one 510(k) clearance for Lasag AG. As of , FDA records show no recalls naming K900199.

Clearance record

Decision date
Received
(70 days to decision)
Product code
HQF Laser, Ophthalmic
Regulation
21 CFR 886.4390
Device class
Class II
Review panel
Ophthalmic
Applicant
Lasag AG 500 Iolab Dr., Claremont CA
Third party review
No

Clearances, product code HQF

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