ZEST PLANT— 510(k) K801524

Name: FDA 510(k) clearance K801524
Creator: U.S. Food and Drug Administration
Published: 1980-07-21

Substantially Equivalent

Zest Anchors, Inc.

FDA 510(k) clearance K801524 for ZEST PLANT, Substantially Equivalent on 1980-07-21. Applicant: Zest Anchors, Inc.. Device class: 2.

Clearance details

Applicant: Zest Anchors, Inc.
Product code: Code DZE
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1980-07-01
Decision date: 1980-07-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZE

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K260463 — ZEROS Dental Implant System2026-08-19
K251188 — UNIQA® Dental Implants System2026-06-25
K250806 — Dental Implant System2026-06-18
K251232 — MegaGen Zygoma Dental Implant System2026-06-18
K260006 — INOSS System2026-06-17

More clearances from Zest Anchors, Inc.

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K150295 — LOCATOR RTx2015-07-24
K083324 — LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM2009-02-25
K072878 — MODIFICATION TO: LOCATOR IMPLANT ANCHOR2007-12-03
K042466 — X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE2004-11-24
K033699 — LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 085862004-04-22

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.