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
K000233Substantially Equivalent

Menicon Sf-P

Menicon Co. Ltd., Wilmington MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000233 is the FDA 510(k) clearance record for MENICON SF-P, a class II device, cleared for Menicon Co, Ltd. on under FDA product code HQD (Lens, Contact (Other Material) - Daily). FDA records list 18 510(k) clearances for Menicon Co, Ltd., from to . As of , FDA records show no recalls naming K000233.

Clearance record

Decision date
Received
(113 days to decision)
Product code
HQD Lens, Contact (Other Material) - Daily
Regulation
21 CFR 886.5916
Device class
Class II
Review panel
Ophthalmic
Applicant
Menicon Co, Ltd. 269 A Ballardvale St., Wilmington MA
510(k) summary
Summary
Third party review
No

Clearances, product code HQD

Trailing 12 months
1 clearance under product code HQD in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HQD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260