LNLUnclassified

Stimulator, Electrical For Sperm Collection

Unknown

LNL is the FDA product code for Stimulator, Electrical For Sperm Collection. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1997-09-18, and no recalls.

Classification record

Product code: LNL
Device name: Stimulator, Electrical For Sperm Collection
Device class: Unclassified
Review panel: Unknown
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code LNL

By decision year

1 clearance under product code LNL with a decision year between 1997 and 1997, 1997 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code LNL by decision year
Year	Clearances
1997	1

Applicants with the most clearances

Product code LNL

Applicants holding the most 510(k) clearances under product code LNL
Applicant	Clearances
National Rehab Hospital	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Dalzell USA Medical Systems

Recent clearances

Product code LNL

K962379UnclassifiedSeager ElectroejaculatorNational Rehab Hospital / cleared 1997-09-18

Recent recalls

Product code LNL

FDA records show no recalls under product code LNL.

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)