LXQUnclassified

Cup, Eye

Unknown

LXQ is the FDA product code for Cup, Eye. As of 2026-09-10, FDA records hold 5 510(k) clearances under this code, the most recent dated 2015-09-01, and no recalls.

Classification record

Product code: LXQ
Device name: Cup, Eye
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: 5
Ingested recalls: 0

Clearances, product code LXQ

By decision year

5 clearances under product code LXQ with a decision year between 1988 and 2015, 1988 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code LXQ by decision year
Year	Clearances
1988	1
1997	1
2005	1
2014	1
2015	1

Applicants with the most clearances

Product code LXQ

Applicants holding the most 510(k) clearances under product code LXQ
Applicant	Clearances
Advantage Diagnostics Corp.	1
Apothecary Products, LLC	1
Dynarex Corp.	1
John Branch	1
Tollot Pty.Ltd.(Aaxis Pacific)	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code LXQ

Recent recalls

Product code LXQ

FDA records show no recalls under product code LXQ.

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)