FDA applicant

Wilde-USA, Inc.

Chicago, IL16 decisions1991–19930 recalls

FDA records 16 decisions for Wilde-USA, Inc. (Chicago, IL) from 1991 to 1993: 16 510(k) clearances. Most are in product codes EBI (Resin, Denture, Relining, Repairing, Rebasing) and EBF (Material, Tooth Shade, Resin). 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 Wilde-USA, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wilde-USA, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Wilde-USA”

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

Wilde Dental (Usa) 1

Wilde-USA, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Wilde-USA”