510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K882531Substantially Equivalent

Modified L.j.'s Sex Helper

L.J. Fant & Co., Glencoe AL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K882531 is the FDA 510(k) clearance record for MODIFIED L.J.'S SEX HELPER, a class II device, cleared for L.J. Fant & Co. on under FDA product code LKY (Device, External Penile Rigidity). FDA's definition for product code LKY reads: "Intended to create or maintain sufficient penile rigidity for sexual intercourse. These include vacuum pumps, constriction rings, and penile splints, which are mechanical, powered or pneumatic devices". FDA records list one 510(k) clearance for L.J. Fant & Co. As of , FDA records show no recalls naming K882531.

Clearance record

Decision date
Received
(169 days to decision)
Product code
LKY Device, External Penile Rigidity
Regulation
21 CFR 876.5020
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
L.J. Fant & Co. 314 Valley St., Glencoe AL
Third party review
No

Clearances, product code LKY

Trailing 12 months

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

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