FDA applicant

Tucker & Associates

Green Valley, AZ4 decisions1997–20040 recalls

FDA records 4 decisions for Tucker & Associates (Green Valley, AZ) from 1997 to 2004: 4 510(k) clearances. Most are in product codes FXX (Mask, Surgical) and LZB (Finger Cot). Its devices cite 2 predicates, 1 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, general and plastic surgery panel, where it files most

How often FDA has decided Tucker & Associates’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tucker & Associates since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Tucker & Associates’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Tucker”

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

Tucker Designs, Ltd. 1

Tucker & Associates

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Tucker”