FDA applicant

Novus Monitoring, Ltd.

United Kingdom, GB2 decisions2002–20040 recalls

FDA records 2 decisions for Novus Monitoring, Ltd. (United Kingdom, GB) from 2002 to 2004: 2 510(k) clearances. All are in product code GWM (Device, Monitoring, Intracranial Pressure). Its devices cite 7 predicates, 1 of them its own earlier devices. 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, neurology panel, where it files most

How often FDA has decided Novus Monitoring, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Novus Monitoring, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Novus Monitoring, Ltd.’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 “Novus”

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

Novus Scientific AB 3 Novus Technologies, Inc. 1

Novus Monitoring, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Novus”