MICRO-VENT— 510(k) K864321

Name: FDA 510(k) clearance K864321
Creator: U.S. Food and Drug Administration
Published: 1987-01-07

Substantially Equivalent

Core-Vent Corp.

FDA 510(k) clearance K864321 for MICRO-VENT, Substantially Equivalent on 1987-01-07. Applicant: Core-Vent Corp.. Device class: 2.

Clearance details

Applicant: Core-Vent Corp.
Product code: Code DZE
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1986-11-03
Decision date: 1987-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Encino, CA, 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 Core-Vent Corp.

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K002614 — ADVENT IMPLANT SYSTEM2000-12-08
K002188 — SWISSPLUS IMPLANT SYSTEM, MODEL SPWB 8,10,12,14/OPH20/SMPR, SPB 8,10,12,14/OP3.5D/OPAR,OPB 8,10,12,14/OP2.3D/OP2.8D,2000-10-30
K950575 — BIO-VENT IMPLANT1995-07-11
K950576 — BIO-VENT X IMPLANT1995-07-11
K950577 — SWEDE-VENT IMPLANT1995-07-11

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.