510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923500Substantially Equivalent

Beausoleil Frame

Oliver Peoples, Inc., Los Angeles CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923500 is the FDA 510(k) clearance record for BEAUSOLEIL FRAME, a class I device, cleared for Oliver Peoples, Inc. on under FDA product code HQZ (Frame, Spectacle). FDA records list 2 510(k) clearances for Oliver Peoples, Inc., from to . As of , FDA records show no recalls naming K923500.

Clearance record

Decision date
Received
(216 days to decision)
Product code
HQZ Frame, Spectacle
Regulation
21 CFR 886.5842
Device class
Class I
Review panel
Ophthalmic
Applicant
Oliver Peoples, Inc. 8600 Sunset Blvd., Los Angeles CA
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