HDIClass II

Hook, Destructive, Obstetrical

21 CFR 884.4500 / Obstetrics/Gynecology

HDI is the FDA product code for Hook, Destructive, Obstetrical, a class II device type, regulated under 21 CFR 884.4500. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: HDI
Device name: Hook, Destructive, Obstetrical
Regulation: 21 CFR 884.4500
Device class: Class II
Review panel: Obstetrics/Gynecology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: 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 HDI.

Recent clearances

Product code HDI

FDA records hold no clearances under product code HDI.

Recent recalls

Product code HDI

FDA records show no recalls under product code HDI.

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)