FDA applicant

Roger Cestac & Assoc.

Mchenry, IL2 decisions1981–19810 recalls

FDA records 2 decisions for Roger Cestac & Assoc. (Mchenry, IL) in 1981: 2 510(k) clearances. Most are in product codes IQI (Orthosis, Limb Brace) and IPT (Orthosis, Thoracic). 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 Roger Cestac & Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Roger Cestac & Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Roger Cestac & 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 “Roger”

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

Roger L. Goodman, D.D.S., P.C. 1

Roger Cestac & Assoc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Roger”