FDA applicant

Wonder Wire

Wyomissing, PA2 decisions1987–19930 recalls

FDA records 2 decisions for Wonder Wire (Wyomissing, PA) from 1987 to 1993: 2 510(k) clearances. Most are in product codes DZC (Wire, Orthodontic) and EJZ (Knife, Margin Finishing, Operative). 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 Wonder Wire’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wonder Wire since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Wonder”

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

Wonder & Bioenergy Hi-Tech America, Inc. 1

Wonder Wire

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Wonder”