DZHClass II

Saw, Bone, Ac-Powered

21 CFR 872.4120 / Dental

DZH is the FDA product code for Saw, Bone, Ac-Powered, a class II device type, regulated under 21 CFR 872.4120. As of 2026-09-10, FDA records hold 4 510(k) clearances under this code, the most recent dated 2003-11-13, and no recalls.

Classification record

Product code: DZH
Device name: Saw, Bone, Ac-Powered
Regulation: 21 CFR 872.4120
Device class: Class II
Review panel: Dental
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 4
Ingested recalls: 0

Clearances, product code DZH

By decision year

4 clearances under product code DZH with a decision year between 1976 and 2003, 1976 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code DZH by decision year
Year	Clearances
1976	2
1994	1
2003	1

Applicants with the most clearances

Product code DZH

Applicants holding the most 510(k) clearances under product code DZH
Applicant	Clearances
American Safety Equipment Corp.	2
Dentatus USA Ltd.	1
Osada Electric Co., Ltd.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code DZH

Recent recalls

Product code DZH

FDA records show no recalls under product code DZH.

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)