FDA applicant

Neoforce Group, Inc.

Ivyland, PA7 decisions2006–20110 recalls

FDA records 7 decisions for Neoforce Group, Inc. (Ivyland, PA) from 2006 to 2011: 7 510(k) clearances. Most are in product codes BYE (Attachment, Breathing, Positive End Expiratory…) and BTM (Ventilator, Emergency, Manual (Resuscitator)). Its devices cite 17 predicates, 6 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, anesthesiology panel, where it files most

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

FDA decisions per year

3in 2011

2007high 3 (2011) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Neoforce Group, Inc.

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?