FDA applicant

Cleft Palate Appliances, Inc.

London, CA1 decision1997–19970 recalls

FDA records 1 decision for Cleft Palate Appliances, Inc. (London, CA) in 1997: 1 510(k) clearance. All are in product code DYJ (Retainer, Screw Expansion, Orthodontic). 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 Cleft Palate Appliances, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cleft Palate Appliances, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cleft Palate Appliances, Inc.

Which product codes does it file in?

What has FDA decided for it lately?