FDA applicant

Chapel and Assoc.

Denton, TX1 decision1998–19980 recalls

FDA records 1 decision for Chapel and Assoc. (Denton, TX) in 1998: 1 510(k) clearance. All are in product code LYT (Fixation Accessory). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Chapel and Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Chapel and Assoc.

Which product codes does it file in?

What has FDA decided for it lately?