FDA applicant

Core Medical, Inc.

Concord, NC3 decisions1992–19920 recalls

FDA records 3 decisions for Core Medical, Inc. (Concord, NC) in 1992: 3 510(k) clearances. Most are in product codes FCG (Biopsy Needle) and GDF (Guide, Needle, Surgical). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Core Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Core Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Core Medical, Inc. 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”

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

Core-Vent Corp. 25 Core Dynamics, Inc. 23 Core Essence Orthopaedics, LLC 6 Core-M, Inc. 4 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 Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Core”