510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920861Substantially Equivalent

Woodlyn Classic Lensmeter

Woodlyn, Inc., Arlington Heights IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920861 is the FDA 510(k) clearance record for WOODLYN CLASSIC LENSMETER, a class I device, cleared for Woodlyn, Inc. on under FDA product code HLM (Instrument, Measuring, Lens, Ac-Powered). FDA records list 19 510(k) clearances for Woodlyn, Inc., from to . As of , FDA records show no recalls naming K920861.

Clearance record

Decision date
Received
(156 days to decision)
Product code
HLM Instrument, Measuring, Lens, Ac-Powered
Regulation
21 CFR 886.1425
Device class
Class I
Review panel
Ophthalmic
Applicant
Woodlyn, Inc. 2920 Malmo Dr., Arlington Heights IL
510(k) summary
Summary
Third party review
No

Clearances, product code HLM

Trailing 12 months

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

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