REXNot classified

Ir Laser Illuminator Only/Night Vision System

Unknown

REX is the FDA product code for Ir Laser Illuminator Only/Night Vision System. FDA's definition for this code reads: "Product, laser, infrared, illuminator only, viewed through night-vision equipment". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: REX
Device name: Ir Laser Illuminator Only/Night Vision System
FDA definition: Product, laser, infrared, illuminator only, viewed through night-vision equipment
Device class: Not classified
Review panel: Unknown
Submission type: FDA code null
GMP exempt: Yes
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

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

Recent clearances

Product code REX

FDA records hold no clearances under product code REX.

Recent recalls

Product code REX

Z-0654-2013Class IIThese camera systems were manufactured by LMGS and found to fail to comply with the FDA laser performance standard during an FDA...Lockheed Martin Gyrocam Systems, Inc. / initiated 2010-01-21 / 33 units

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)