DZSClass I

Capsule, Dental, Amalgam

21 CFR 872.3110 / Dental

DZS is the FDA product code for Capsule, Dental, Amalgam, a class I device type, regulated under 21 CFR 872.3110. As of 2026-09-10, FDA records hold 4 510(k) clearances under this code, the most recent dated 1982-09-14, and no recalls.

Classification record

Product code: DZS
Device name: Capsule, Dental, Amalgam
Regulation: 21 CFR 872.3110
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: 4
Ingested recalls: 0

Clearances, product code DZS

By decision year

4 clearances under product code DZS with a decision year between 1978 and 1982, 1978 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code DZS by decision year
Year	Clearances
1978	2
1980	1
1982	1

Applicants with the most clearances

Product code DZS

Applicants holding the most 510(k) clearances under product code DZS
Applicant	Clearances
Lee Pharmaceuticals	2
Johnson & Johnson Professionals, Inc.	1
Syntex Dental Products, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 19 companies shown, in name order

Recent clearances

Product code DZS

Recent recalls

Product code DZS

FDA records show no recalls under product code DZS.

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)