FDA applicant

Nova-Ventrx

Wheeling, IL12 decisions1981–19970 recalls

FDA records 12 decisions for Nova-Ventrx (Wheeling, IL) from 1981 to 1997: 12 510(k) clearances. Most are in product codes BZO (Set, Tubing And Support, Ventilator (W Harness)) and BTT (Humidifier, Respiratory Gas, (Direct Patient…). 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, anesthesiology panel, where it files most

How often FDA has decided Nova-Ventrx’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nova-Ventrx since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Nova-Ventrx’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Nova-Ventrx”

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

Nova Biomedical Corp. 129 Nova Medical Specialties 11 Nova Technology Corp. 3 Nova Health Systems, Inc. 3 Nova Medical, Inc. 1 Nova Corp. 1 Nova Technologies, Inc. 1 Nova/Da Vinci Systems, Inc. 1 Nova Design Technologies, Ltd. 1 Nova Therapeutic System 1 Nova Ranger, Inc. 1 Nova Rubber Glove Industries Sdn. Bhd. 1

Nova-Ventrx

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nova-Ventrx”