510(k) Report

FDA applicant

Aseptic Dental Technologies, Inc.

Arlington Heights, IL1 decision1992–19920 recalls

FDA records 1 decision for Aseptic Dental Technologies, Inc. (Arlington Heights, IL) in 1992: 1 510(k) clearance. All are in product code DZM (Needle, Dental). 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 Aseptic Dental Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aseptic Dental Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Aseptic Dental Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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