REONot classified

Analytical Measuring And Detection Laser Product

Unknown

REO is the FDA product code for Analytical Measuring And Detection Laser Product. FDA's definition for this code reads: "Product, laser, instrument, analyze/detect chemical species". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: REO
Device name: Analytical Measuring And Detection Laser Product
FDA definition: Product, laser, instrument, analyze/detect chemical species
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 REO.

Recent clearances

Product code REO

FDA records hold no clearances under product code REO.

Recent recalls

Product code REO

Z-2600-2011It was discovered The Prism 7642 was not certified at the time of delivery. The product lacks the required labeling and the...American Stress Technologies, Inc. / initiated 2011-04-27 / 1

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)