FDA applicant
Northwest Orthodontics, Inc.
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
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.
Planning a device like Northwest Orthodontics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Northwest”
FDA records each applicant name separately; these may or may not be the same firm.