FDA applicant

Dale Miller, Inc. - the Chin-Up Company

Dracula, GA1 decision2004–20040 recalls

FDA records 1 decision for Dale Miller, Inc. - the Chin-Up Company (Dracula, GA) in 2004: 1 510(k) clearance. All are in product code LWF (Dilator, Nasal). 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, ear, nose and throat panel, where it files most

How often FDA has decided Dale Miller, Inc. - the Chin-Up Company’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dale Miller, Inc. - the Chin-Up Company since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dale Miller, Inc. - the Chin-Up Company by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Dale Miller, Inc. - the Chin-Up Company’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 “Dale”

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

Dale Medical Products, Inc. 13 Dale T. Dupuis 3

Dale Miller, Inc. - the Chin-Up Company

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dale”