FDA applicant

Artech Corp.

Chantilly, VA8 decisions1984–19920 recalls

FDA records 8 decisions for Artech Corp. (Chantilly, VA) from 1984 to 1992: 8 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and DZJ (Driver, Wire, And Bone Drill, Manual). 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 Artech Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Artech Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Artech 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?