DIA ANATOMIC ABUTMENT— 510(k) K902433

Name: FDA 510(k) clearance K902433
Creator: U.S. Food and Drug Administration
Published: 1992-01-17

Substantially Equivalent

Dental Imaging Assoc., Inc.

FDA 510(k) clearance K902433 for DIA ANATOMIC ABUTMENT, Substantially Equivalent on 1992-01-17. Applicant: Dental Imaging Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Dental Imaging Assoc., Inc.
Product code: Code DZE
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1990-05-31
Decision date: 1992-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Torrance, CA, US

Download summary PDF View on FDA.gov ↗

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K250806 — Dental Implant System2026-06-18
K251232 — MegaGen Zygoma Dental Implant System2026-06-18
K260006 — INOSS System2026-06-17

More clearances from Dental Imaging Assoc., Inc.

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K902434 — DIA HEALING CAP1991-02-27
K902435 — DIA IMPRESSION COPING1991-02-20

Adverse events under product code DZE

product code DZE

Death: 28
Injury: 3,367,041
Malfunction: 19,958
Other: 13
Total: 3,387,040

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.