FDA applicant

Core-Vent Corp.

Encino, CA25 decisions1986–20000 recalls

FDA records 25 decisions for Core-Vent Corp. (Encino, CA) from 1986 to 2000: 25 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and EFS (Unit, Oral Irrigation). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Core-Vent Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Core-Vent Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Core-Vent Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Core-Vent”

FDA records each applicant name separately; these may or may not be the same firm.

Core Dynamics, Inc. 23 Core Essence Orthopaedics, LLC 6 Core-M, Inc. 4 Core Medical, Inc. 3 Core-Nexus 2 Core-Vent Bio-Engineering, Inc. 1 Core 3D Protech, S.L. 1 Core Healthcare, Ltd. 1 Core Access Surgical Technologies, Inc. 1 Core Scientific, Ltd. 1 Core Scientific Creation, Ltd. 1

Core-Vent Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Core-Vent”