FDA applicant

Moberg Medical, Inc.

Ambler, PA2 decisions1992–19960 recalls

FDA records 2 decisions for Moberg Medical, Inc. (Ambler, PA) from 1992 to 1996: 2 510(k) clearances. Most are in product codes GWQ (Full-Montage Standard Electroencephalograph) and GWF (Stimulator, Electrical, Evoked Response). Its devices cite 2 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 Moberg Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Moberg Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Moberg”

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

Moberg Research, Inc. 2

Moberg Medical, 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?

Other applicant names beginning “Moberg”