DB PRECISION IMPLANT SYSTEM, 2000 SERIES— 510(k) K860982

Name: FDA 510(k) clearance K860982
Creator: U.S. Food and Drug Administration
Published: 1986-04-25

Substantially Equivalent

Driskell Bioengineering

FDA 510(k) clearance K860982 for DB PRECISION IMPLANT SYSTEM, 2000 SERIES, Substantially Equivalent on 1986-04-25. Applicant: Driskell Bioengineering. Device class: 2.

Clearance details

Applicant: Driskell Bioengineering
Product code: Code DZE
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1986-03-17
Decision date: 1986-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Galena, OH, 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 Driskell Bioengineering

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K875242 — DB PRECISION IMPLANT SYSTEM, 1000 SERIES W/HAC1988-02-26
K875243 — DB PRECISION IMPLANT SYSTEM, 2000 SERIES W/HAC1988-02-26
K853788 — DB PRECISION IMPLANT SYSTEM1985-10-31

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.