RIONot classified

Led Toys And Entertainment Products

Unknown

RIO is the FDA product code for Led Toys And Entertainment Products. FDA's definition for this code reads: "Products that incorporate light emitting diodes (LEDs) to be used in toys or entertaiment products to control, illuminate, or interact with the user. These products include LED "lasertag" toys, and blacklights for home use". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: RIO
Device name: Led Toys And Entertainment Products
FDA definition: Products that incorporate light emitting diodes (LEDs) to be used in toys or entertaiment products to control, illuminate, or interact with the user. These products include LED "lasertag" toys, and blacklights for home use.
Device class: Not classified
Review panel: Unknown
Submission type: FDA code null
GMP exempt: Yes
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

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

Recent clearances

Product code RIO

FDA records hold no clearances under product code RIO.

Recent recalls

Product code RIO

FDA records show no recalls under product code RIO.

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)