510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771933Substantially Equivalent

Cilco Anterior Chamber Lens

California Intraocular Lens, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771933 is the FDA 510(k) clearance record for CILCO ANTERIOR CHAMBER LENS, a class III device, cleared for California Intraocular Lens on under FDA product code HQL (Intraocular Lens). FDA records list one 510(k) clearance for California Intraocular Lens. As of , FDA records show no recalls naming K771933.

Clearance record

Decision date
Received
(104 days to decision)
Product code
HQL Intraocular Lens
Regulation
21 CFR 886.3600
Device class
Class III
Review panel
Ophthalmic
Applicant
California Intraocular Lens 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HQL

Trailing 12 months

FDA records hold no clearances under product code HQL in the trailing twelve months.

FDA records show no clearances under product code HQL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HQL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260