FDA applicant

Moberg Research, Inc.

Ambler, PA2 decisions2008–20191 recall

FDA records 2 decisions for Moberg Research, Inc. (Ambler, PA) from 2008 to 2019: 2 510(k) clearances. Most are in product codes OMA (Amplitude-Integrated Electroencephalograph) and OLT (Non-Normalizing Quantitative…). Its devices cite 11 predicates, 1 of them its own earlier devices. 1 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 Moberg Research, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

1in 2023

2008high 1 (2023) · low 0 (2008)2026

Class I Class II/III not classified

FIG. 1 — Moberg Research, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Moberg Research, Inc.’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 “Moberg”

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

Moberg Medical, Inc. 2

Moberg Research, 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?

What has been recalled?

Other applicant names beginning “Moberg”