FDA applicant

Vlv Associates, Inc.

East Hanover, NJ12 decisions1986–19970 recalls

FDA records 12 decisions for Vlv Associates, Inc. (East Hanover, NJ) from 1986 to 1997: 12 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and KMK (Device, Intravascular Catheter Securement). 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 Vlv Associates, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vlv Associates, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vlv Associates, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?