510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K860954Substantially Equivalent

Spectacles Frame

Roseburg SA, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860954 is the FDA 510(k) clearance record for SPECTACLES FRAME, a class I device, cleared for Roseburg SA on under FDA product code HQZ (Frame, Spectacle). FDA records list 24 510(k) clearances for Roseburg SA, from to . As of , FDA records show no recalls naming K860954.

Clearance record

Decision date
Received
(18 days to decision)
Product code
HQZ Frame, Spectacle
Regulation
21 CFR 886.5842
Device class
Class I
Review panel
Ophthalmic
Applicant
Roseburg SA Suite 120 Canal Sq., Washington DC
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