DZPClass I

Instrument, Diamond, Dental

21 CFR 872.4535 / Dental

DZP is the FDA product code for Instrument, Diamond, Dental, a class I device type, regulated under 21 CFR 872.4535. As of 2026-09-10, FDA records hold 21 510(k) clearances under this code, the most recent dated 2012-04-20, and no recalls.

Classification record

Product code: DZP
Device name: Instrument, Diamond, Dental
Regulation: 21 CFR 872.4535
Device class: Class I
Review panel: Dental
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 21
Ingested recalls: 0

Clearances, product code DZP

By decision year

21 clearances under product code DZP with a decision year between 1976 and 2012, 1983 the highest year at 3.

Show the numbers

510(k) clearances under FDA product code DZP by decision year
Year	Clearances
1976	1
1978	1
1980	2
1983	3
1985	1
1987	1
1988	1
1989	2
1990	3
1992	1
1993	1
1994	3
2012	1

Applicants with the most clearances

Product code DZP

Applicants holding the most 510(k) clearances under product code DZP
Applicant	Clearances
Shofu Dental Corp.	4
Beavers Dental, Div. Sybron Canada, Ltd.	2
Swiss American Metal Craft Corp.	2
Adp Intl., Inc.	1
Alpha Industrializacao de Metais Ltda.	1
Diamond Rotary and Carbide Intl.	1
Dunhall Pharmaceuticals, Inc.	1
E&D Dental Manufacturing Co.	1
Eare Consulting Service	1
Kab Gloves Unltd.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 111 companies shown, in name order