LRLUnclassified

Cushion, Hemorrhoid

Unknown

LRL is the FDA product code for Cushion, Hemorrhoid. As of 2026-09-10, FDA records hold 3 510(k) clearances under this code, the most recent dated 2007-12-07, and no recalls.

Classification record

Product code: LRL
Device name: Cushion, Hemorrhoid
Device class: Unclassified
Review panel: Unknown
Submission type: FDA code 7
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 3
Ingested recalls: 0

Clearances, product code LRL

By decision year

3 clearances under product code LRL with a decision year between 1987 and 2007, 1987 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code LRL by decision year
Year	Clearances
1987	1
1993	1
2007	1

Applicants with the most clearances

Product code LRL

Applicants holding the most 510(k) clearances under product code LRL
Applicant	Clearances
Chi'Am Intl.	1
Health Aid Products	1
Hemaway, LLC	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code LRL

Recent recalls

Product code LRL

FDA records show no recalls under product code LRL.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)