EXXClass I

Probe, Rectal, Non-Powered

21 CFR 876.4730 / Gastroenterology, Urology

EXX is the FDA product code for Probe, Rectal, Non-Powered, a class I device type, regulated under 21 CFR 876.4730. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: EXX
Device name: Probe, Rectal, Non-Powered
Regulation: 21 CFR 876.4730
Device class: Class I
Review panel: Gastroenterology, Urology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 40 companies shown, in name order

Recent clearances

Product code EXX

FDA records hold no clearances under product code EXX.

Recent recalls

Product code EXX

Z-1206-2010Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the...Marina Medical Instruments Inc. / initiated 2009-04-09 / 47

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)