510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K010986Substantially Equivalent

Lunapads

Lunapads International Products, Ltd., Vancouver Bc, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K010986 is the FDA 510(k) clearance record for LUNAPADS, a class I device, cleared for Lunapads International Products, Ltd. on under FDA product code NUQ (Pad, Menstrual, Reusable). FDA's definition for product code NUQ reads: "A reusable, unscented menstrual pad which is used to absorb menstrual fluid or other vaginal discharge and is made of common cellulosic or synthetic material with an established safety profile". FDA records list one 510(k) clearance for Lunapads International Products, Ltd. As of , FDA records show no recalls naming K010986.

Clearance record

Decision date
Received
(72 days to decision)
Product code
NUQ Pad, Menstrual, Reusable
Regulation
21 CFR 884.5435
Device class
Class I
Review panel
Obstetrics/Gynecology
Applicant
Lunapads International Products, Ltd. 207 W. 6th Ave., Vancouver Bc, CA
510(k) summary
Statement
Third party review
No

Clearances, product code NUQ

Trailing 12 months

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

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