510(k) Report

FDA applicant

Univ. Dental Assoc. Department of Orthodontics

Buffalo, NY1 decision1996–19960 recalls

FDA records 1 decision for Univ. Dental Assoc. Department of Orthodontics (Buffalo, NY) in 1996: 1 510(k) clearance. All are in product code LRK (Device, Anti-Snoring). 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 Univ. Dental Assoc. Department of Orthodontics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Univ. Dental Assoc. Department of Orthodontics since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Univ. Dental Assoc. Department of Orthodontics by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Univ. Dental Assoc. Department of…’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) Report

Other applicant names beginning “Univ.”

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