510(k) Report

FDA applicant

Northwest Orthodontics, Inc.

Mchenry, IL6 decisions1977–19800 recalls

FDA records 6 decisions for Northwest Orthodontics, Inc. (Mchenry, IL) from 1977 to 1980: 6 510(k) clearances. Most are in product codes DZB (Headgear, Extraoral, Orthodontic) and DYT (Maintainer, Space Preformed, Orthodontic). 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 Northwest Orthodontics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Northwest Orthodontics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Northwest Orthodontics, 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 “Northwest”

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