FDA applicant

Lancer Assoc.

Mchenry, IL2 decisions1983–19840 recalls

FDA records 2 decisions for Lancer Assoc. (Mchenry, IL) from 1983 to 1984: 2 510(k) clearances. Most are in product codes ION (Exerciser, Non-Measuring) and FRZ (Device, Patient Transfer, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Lancer Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lancer Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lancer Assoc.’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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Other applicant names beginning “Lancer”

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

Lancer Orthodontics, Inc. 14

Lancer Assoc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lancer”