RCINot classified

Cephalometric Devices

Unknown

RCI is the FDA product code for Cephalometric Devices. FDA's definition for this code reads: "A device intended for the radiographic visualization and measurement of the dimensions of the human head". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: RCI
Device name: Cephalometric Devices
FDA definition: A device intended for the radiographic visualization and measurement of the dimensions of the human head.
Device class: Not classified
Review panel: Unknown
Submission type: FDA code null
GMP exempt: No
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 RCI.

Recent clearances

Product code RCI

FDA records hold no clearances under product code RCI.

Recent recalls

Product code RCI

FDA records show no recalls under product code RCI.

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)