FDA applicant

Waggoner Product Development

Plano, TX1 decision1998–19980 recalls

FDA records 1 decision for Waggoner Product Development (Plano, TX) in 1998: 1 510(k) clearance. All are in product code EIA (Unit, Operative Dental). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Waggoner Product Development’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Waggoner Product Development since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Waggoner”

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

Waggoner Dental Mfg. 1

Waggoner Product Development

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Waggoner”