510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K933424Substantially Equivalent

Stetson/s.loren/h.bazaar/g.vanderbilt/p.balmain

Zyloware LLC, Long Island City NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933424 is the FDA 510(k) clearance record for STETSON/S.LOREN/H.BAZAAR/G.VANDERBILT/P.BALMAIN, a class I device, cleared for Zyloware Corp. on under FDA product code HQZ (Frame, Spectacle). FDA records list one 510(k) clearance for Zyloware Corp. As of , FDA records show no recalls naming K933424.

Clearance record

Decision date
Received
(69 days to decision)
Product code
HQZ Frame, Spectacle
Regulation
21 CFR 886.5842
Device class
Class I
Review panel
Ophthalmic
Applicant
Zyloware Corp. 11-36 46th Rd., Long Island City NY
510(k) summary
Statement
Third party review
No

Clearances, product code HQZ

Trailing 12 months

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

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