FDA applicant

Vivus, Inc.

Mountain View, CA2 decisions1996–20000 recalls

FDA records 2 decisions for Vivus, Inc. (Mountain View, CA) from 1996 to 2000: 2 510(k) clearances. All are in product code LKY (Device, External Penile Rigidity). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Vivus, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vivus, Inc.

Which product codes does it file in?

What has FDA decided for it lately?