LNYClass III

Catheter, Percutaneous, Long Term, Intraspinal

Unknown

LNY is the FDA product code for Catheter, Percutaneous, Long Term, Intraspinal, a class III device type. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: LNY
Device name: Catheter, Percutaneous, Long Term, Intraspinal
Device class: Class III
Review panel: Unknown
Submission type: PMA
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

Alcyone Therapeutics, Inc.

Recent clearances

Product code LNY

FDA records hold no clearances under product code LNY.

Recent recalls

Product code LNY

Z-0856-04Some of the outer product pouches have voids in the seals and do not assure that the outer surfaces of the inner tray containing...Deltec, Inc / initiated 2004-03-29

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)