510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K910179Substantially Equivalent

Optical Frame

Australian Optical Co., Inc., Kansas City MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910179 is the FDA 510(k) clearance record for OPTICAL FRAME, a class I device, cleared for Australian Optical Co., Inc. on under FDA product code HQZ (Frame, Spectacle). FDA records list 8 510(k) clearances for Australian Optical Co., Inc., from to . As of , FDA records show no recalls naming K910179.

Clearance record

Decision date
Received
(85 days to decision)
Product code
HQZ Frame, Spectacle
Regulation
21 CFR 886.5842
Device class
Class I
Review panel
Ophthalmic
Applicant
Australian Optical Co., Inc. 1775 Universal Ave., Kansas City MO
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