LQSUnclassified

Spermatocele, Alloplastic

Unknown

LQS is the FDA product code for Spermatocele, Alloplastic. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1986-11-19, and no recalls.

Classification record

Product code: LQS
Device name: Spermatocele, Alloplastic
Device class: Unclassified
Review panel: Unknown
Submission type: 510(k)
Implant: Yes
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code LQS

By decision year

1 clearance under product code LQS with a decision year between 1986 and 1986, 1986 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code LQS by decision year
Year	Clearances
1986	1

Applicants with the most clearances

Product code LQS

Applicants holding the most 510(k) clearances under product code LQS
Applicant	Clearances
Mentor	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LQS.

Recent clearances

Product code LQS

K863565UnclassifiedMentor Alloplastic SpermatoceleMentor Corp. / cleared 1986-11-19

Recent recalls

Product code LQS

FDA records show no recalls under product code LQS.

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)