510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K920170Substantially Equivalent

Spectacle Frame

Sciara Intl., Inc., Springfield Gardens NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920170 is the FDA 510(k) clearance record for SPECTACLE FRAME, a class I device, cleared for Sciara Intl., Inc. on under FDA product code HQZ (Frame, Spectacle). FDA records list one 510(k) clearance for Sciara Intl., Inc. As of , FDA records show no recalls naming K920170.

Clearance record

Decision date
Received
(58 days to decision)
Product code
HQZ Frame, Spectacle
Regulation
21 CFR 886.5842
Device class
Class I
Review panel
Ophthalmic
Applicant
Sciara Intl., Inc. 182-08 149th Ave., Springfield Gardens NY
510(k) summary
Summary
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