FDA applicant

Viggo Products

Madison, WI7 decisions1985–19850 recalls

FDA records 7 decisions for Viggo Products (Madison, WI) in 1985: 7 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and FPA (Set, Administration, Intravascular). 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 hospital panel, where it files most

How often FDA has decided Viggo Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Viggo Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Viggo”

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

Viggo-Spectramed 1

Viggo Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Viggo”