FDA applicant

Vipont Laboratories, Inc.

Mchenry, IL3 decisions1983–19840 recalls

FDA records 3 decisions for Vipont Laboratories, Inc. (Mchenry, IL) from 1983 to 1984: 3 510(k) clearances. All are in product code EFS (Unit, Oral Irrigation). 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 Vipont Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vipont Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vipont Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?