510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K182646Substantially Equivalent

Vitreq disposable laser probes, light fibers and Chandelier

Vitreq BV, Vierpolders, NL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K182646 is the FDA 510(k) clearance record for Vitreq disposable laser probes, light fibers and Chandelier, a class II device, cleared for VitreQ BV on under FDA product code HQB (Photocoagulator And Accessories). FDA records list 2 510(k) clearances for VitreQ BV, from to . As of , FDA records show no recalls naming K182646.

Clearance record

Decision date
Received
(219 days to decision)
Product code
HQB Photocoagulator And Accessories
Regulation
21 CFR 886.4690
Device class
Class II
Review panel
Ophthalmic
Applicant
VitreQ BV Segglant-Noord 2, Vierpolders, NL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HQB

Trailing 12 months

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

FDA records show no clearances under product code HQB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HQB, 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