FDA applicant

Oms Medical Supplies, Inc.

Weymouth, MA6 decisions1988–19960 recalls

FDA records 6 decisions for Oms Medical Supplies, Inc. (Weymouth, MA) from 1988 to 1996: 6 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and IPF (Stimulator, Muscle, Powered). 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 Oms Medical Supplies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Oms Medical Supplies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Oms Medical Supplies, 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

Oms Medical Supplies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?