FHJClass II

Shield, Circumcision

21 CFR 884.4530 / Obstetrics/Gynecology

FHJ is the FDA product code for Shield, Circumcision, a class II device type, regulated under 21 CFR 884.4530. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1990-11-05, and no recalls.

Classification record

Product code: FHJ
Device name: Shield, Circumcision
Regulation: 21 CFR 884.4530
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: No
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code FHJ

By decision year

2 clearances under product code FHJ with a decision year between 1983 and 1990, 1983 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code FHJ by decision year
Year	Clearances
1983	1
1990	1

Applicants with the most clearances

Product code FHJ

Applicants holding the most 510(k) clearances under product code FHJ
Applicant	Clearances
Kedumin Kits, Ltd.	1
Shofu Dental Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

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

Recent clearances

Product code FHJ

Recent recalls

Product code FHJ

FDA records show no recalls under product code FHJ.

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)