FDA applicant

Sensicon Corp.

Vista, CA2 decisions1997–19980 recalls

FDA records 2 decisions for Sensicon Corp. (Vista, CA) from 1997 to 1998: 2 510(k) clearances. All are in product code MOL (Condom, Synthetic). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Sensicon Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Sensicon Corp.

Which product codes does it file in?

What has FDA decided for it lately?