FDA applicant

Venture Molded Products, Inc.

Ewing Township, NJ1 decision1988–19880 recalls

FDA records 1 decision for Venture Molded Products, Inc. (Ewing Township, NJ) in 1988: 1 510(k) clearance. All are in product code 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 Venture Molded Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Venture Molded Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Venture”

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

Venture Technology, Inc. 5 Venture Management Corp. 3 Venture Therapeutics, Inc. 1

Venture Molded Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Venture”